Author: Jackie Harris, Pharm.D, BCPS, Executive Director, MSHP Research and Education Foundation
MSHP R&E Foundation is currently accepting submissions and nominees for several awards.
MSHP R&E Best Practice Award
The Best Practice Award program recognizes innovation and outstanding performance in a pharmacy directed initiative. The theme for the 2020 award focuses on Innovative Stewardship Roles. Submission deadline is December 30th, 2019.
A poster of the program will be highlighted during the Spring Meeting Poster Session. The award recipient will be honored at a Reception during the Spring Meeting and have the opportunity to provide a brief podium presentation detailing the implementation and impact of the project to the attendees.
Applicants will be judged on their descriptions of programs and practices currently employed in their health system based on the following criteria:
· Inventiveness of the program
· Significance of the program to the health system
· Demonstration of benefit to patient care as supported by program evaluation data
· Significance of the program to pharmacy practice
· Quality of submitted program report
· Relevance to other institutions
Applicants must be active MSHP members practicing in a health-system setting such as a large or small hospital, home health, ambulatory clinic or other health care system. More than one successful program from a health system may be submitted for consideration.
Award recipient will receive half off their meeting registration, a plaque and a $250 honorarium.
Submission Instructions: A program summary not to exceed 400 words must be submitted with the application and include the following information.
· Background – description of need for program
· Goals and specific aims of the program
· Program description/methods – description of development process, role(s) of the pharmacist, timeline
· Results - when results are not yet available, include a description of how impact of the program will be measured
· Conclusion – established and/or expected clinical impact of the program
· Submissions may also include any pictures, graphs, figures or data tables that support the summary. Each of these must be clearly labeled and described. Such information will not count against the 400 word limit.
• Email your submission to firstname.lastname@example.org with Best Practice Award Submission in the subject line.
MSHP R&E Best Residency Project Award
The Best Residency Project Award recognizes innovation and outstanding performance in a pharmacy residency project. A poster of the program will be highlighted during the Spring Meeting Poster Session. The award recipient will be honored at a Reception during the Spring Meeting and have the opportunity to provide a brief podium presentation detailing the implementation and impact of the project to the attendees. Submission deadline is December 30th, 2019.
Applicants will be judged based on the following criteria:
· Inventiveness of the project
· Significance of the project to the health system
· Demonstration of benefit to patient care as supported by project evaluation data
· Significance of the project to pharmacy practice
· Quality of submitted project report
Applicants must be active MSHP members completing a residency in a health-system setting such as a large or small hospital, home health, ambulatory clinic or other health care system.
· Background – description of need for project
· Goals and specific aims of the project
· Results - when results are not yet available, include a description of how impact of the project will be measured
· Conclusion – established and/or expected clinical impact of the project
Email your submission to email@example.com with Best Residency Project Award Submission in the subject line.
The Garrison award was established in 1985, named after Thomas Garrison for his long standing support of MSHP (past-president 1974-1976), ASHP (past-president 1984) and numerous professional and academic contributions to Pharmacy. The Garrison Award is presented each year to a deserving candidate who has been nominated in recognition of sustained contributions in multiple areas:
· Outstanding accomplishment in practice in health-system pharmacy;
· Outstanding poster or spoken presentation at a state or national meeting;
· Publication in a nationally recognized pharmacy or medical journal;
· Demonstrated activity with pharmacy students from St. Louis or the UMKC Schools of Pharmacy;
· Development of an innovative service in a health-system pharmacy in either education, administration, clinical service, or distribution;
· Contributions to the profession through service to ASHP, MSHP and/or local affiliates.
Each letter of nomination must include:
· Name, work address, and telephone number of nominee;
· Name, work address, and telephone number of nominator;
· Sufficient explanation and documentation of the nominee’s accomplishment(s) to allow a proper decision by the selection committee;
· and Curriculum Vitae of the Nominee.
· To be considered for the Garrison Award, the nominee must be a current active member of the Missouri Society of Health-System Pharmacists. The winner will be selected by the Board of Directors of the MSHP Research and Education Foundation. Email your nomination to firstname.lastname@example.org with Garrison Award Submission in the subject line.
Submission Deadline for Garrison Award is January 31, 2020.
Authors: Shu-wen Tran, B.S., UMKC PharmD Candidate 2020 and Diana Tamer, B.S., Pharm.D., BCOP
How is it possible that patients with certain metastatic cancers are still treated with traditional chemotherapy when targeted precision medicine is available for them as first line agents? While sequencing the whole genome led to having technologies today to sequence each patient’s tumor DNA, and finding targeted therapies for tumorigenesis driving mutations; these therapies are costly and not affordable to most patients—even those with insurance coverage. Is there any way to drive down the cost of oncolytic agents? Let’s explore some avenues.
Targeted therapy, otherwise known as precision medicine, are medications designed to specifically target driving mutation(s) that is/are causing the cancer type. Targeted therapy differs from traditional therapy in that they act on a specific pathway or gene mutation related to the cancer type instead of acting systemically, affecting all normal and abnormal cells. Over the past 10 years, the FDA has approved more than 80 targeted oncolytic therapies, with more than half of them approved for oral administration.1 It is important to understand that traditional chemotherapies remain the standard of care in early stages of cancer, while targeted drug therapies are options for patients with metastatic disease—if they harbor a particular mutation. That is also partly because as new drugs are studied in clinical trials for cancer patients, they start testing them in patients that have no other options and are at more advanced stages of their disease. That being said, as these drugs gain approval, clinical trials in earlier stages of the disease are underway; which will lead to maybe more use of these agents at all stages of cancer.
Disparities in insurance plan coverage for cancer treatment is one of the most challenging aspects patients are facing. Patients are faced with a financial burden when their plan coverage diverges (medical versus pharmacy benefit), and their oral cancer drug therapy treatment is submitted through their pharmacy benefit, instead of their medical benefit. Often times a set-back in cancer treatment occurs because they are unable to afford therapy. So why is this happening?
“Medical benefits often require patients to pay a flat copayment (perhaps $20 to $50 per visit) for care in an outpatient setting, which can include administration of intravenous medications. Pharmacy benefits, by contrast, often have a tiered copayment structure and other provisions that increase cost sharing for more expensive medications. Pharmacy benefits may include coinsurance (in which patients are responsible for a percentage of the medication cost), high overall deductibles, and caps on annual drug benefits.”2 Most insurance plans place oral cancer agents into a “specialty tier” or “fourth tier,” which may require a cost-sharing responsibility for the patient of anywhere from 25 to 33 percent of the cost of the drug, leading to copays which can range from$150-$7,000 per month. And these medications are taken chronically, typically on a daily basis, until disease progression, unacceptable toxicity, or death. And a common question that patient ask in clinic is: “What would I do when I can no longer afford this treatment?”
In 2013, the Cancer Drug Parity Act3 was first introduced to Congress. The purpose of this bill is to help ensure that patients will not pay more for oral chemotherapy agents under their pharmacy benefit than they would for an intravenous chemotherapy agent under their medical benefit. One might wonder, don’t we have something like this in effect? Well, yes—in 43 states. Since 2007, many states have passed their own oral parity law, but it only applies to state health plans, leaving out patients under self-funded and fully insured health plans. If Congress approves this bill, the new federal legislation will require all health plans, including the remaining seven states to adopt this cancer drug parity act. Currently, seven states have yet to adopt this cancer drug parity act: Alabama, Idaho, Michigan, Montana, North Carolina, South Carolina, and Tennessee4.
In a retrospective claims analysis published by Dr. Dusetzina and colleagues5, authors found that oral chemotherapy parity laws showed only “modest” financial benefit for patients. Their analysis encompassed 63,780 patients from three nationwide insurers (Aetna, Humana, and UnitedHealthcare), comparing effects before and after oral chemotherapy parity laws. Patients that were studied lived in one of 16 states that had implemented oral chemotherapy parity laws from July 2008 to July 2012, and who were receiving chemotherapy treatment. Results showed an increase in patient out-of-pocket (OOP) spend of more than $100 per month in plans subject to parity versus a slight decline in plans not subject to parity (8.4% to 11.1% vs. 12.0% to 11.7%, p=0.004). Monthly patient OOP spend on oral chemotherapy agents showed a decline in plans subject to parity in the 25th-, 50th-, and 75th percentile ($19.44, $32.13, $10.83, p<0.001), but saw an increase at the 90th- and 95th percentile ($37.19, $143.25, p<0.001). Dr. Dusetzina and colleagues conclude that “these laws alone may be insufficient to ensure that patients are protected from high out-of-pocket costs.”
So what should we do? As more and more precision, targeted therapies are being pumped into the market, cancer patients should not have to pay any less for their oral cancer drug treatment under their pharmacy benefit than they would under their medical benefit. It is currently unclear exactly how many patients will benefit from this bill. This federal act is a start to help patients gain access to precision medicine. The underlying issue may be the price of the agents themselves. But that’s another article for another time.
Authors: Marissa Chow, Pharm.D. Candidate Class of 2021 and
Emily Shor, Pharm. D.
Patients with malignancies have a 20% to 30% increased risk for venous thromboembolism (VTE), such as deep vein thrombosis (DVT) and pulmonary embolism (PE), due to their hypercoagulable state.1-3 Additionally, a VTE at the time of or within one year of cancer diagnosis is correlated with more advanced stages of cancer and increased risk of death.4 The 2019 NCCN and 2016 CHEST guidelines recommend that patients with a cancer associated VTE be anticoagulated for at least three months or indefinitely while cancer is active, patient is undergoing treatment, or risk factors remain present.2-3,5 However, the NCCN guidelines do not provide recommendations regarding routine VTE prophylaxis in ambulatory cancer patients unless they have certain risk factors, such as certain cancer types and/or chemotherapy agents. 2 Managing cancer-associated thrombosis (CAT) must balance both a patient’s increased risk of recurrent VTE patients alongside risks of bleeding.
The CLOT trial established low-molecular-weight heparin (LMWH) as first line therapy for chronic anticoagulation therapy in patients with metastatic disease with acute VTE.6 Despite frequent self-injections, which can affect patient adherence, LMWHs have a faster onset and reaches steady state more quickly than vitamin K antagonists.7 Moreover, dalteparin significantly decreased risk of recurrent VTE compared to oral anticoagulants.6 While warfarin offers an oral alternative, it can be difficult to maintain a therapeutic INR due to frequent follow-up, drug-drug interactions with chemotherapy agents, malnutrition, and possible liver dysfunction.
Since their development, utilization of direct oral anticoagulants (DOACs) has greatly increased as their efficacy and safety were established in the setting of VTE treatment within the general population in various landmark trials. DOACs do not require frequent lab monitoring and have few drug-food interactions. However, until recently, the role of DOACs in CAT has been unclear due to limited evidence from subgroup analyses of cancer patients in each DOAC’s landmark trials. Although DOACs offer more convenient administration, further investigation of the role of DOACs as effective and safe agents in the prophylaxis and treatment of VTE in cancer patients is needed. This article will review the recently published literature regarding the use of DOACs in cancer patients.
VTE Treatment in Cancer Patients
The studies assessing the efficacy and safety of DOACs for VTE treatment in the general population had limited enrollment of cancer patients, ranging from 3% to 9%.8-11 Subgroup analyses of these patients show promising results, but the enrolled cancer patients likely had a lower risk profile. Randomized trials have recently assessed the role of apixaban, rivaroxaban, and edoxaban in CAT treatment as compared to the efficacy and safety of utilizing therapeutic dosing of a LMWH, dalteparin.
Apixaban: ADAM VTE12
The ADAM VTE Trial, a multicenter, open-label trial, randomized patients with cancer-associated acute VTE to receive dalteparin or apixaban (10 mg twice daily for seven days followed by 5 mg twice daily). The most frequent types of cancer were colorectal, lung, pancreas, and breast cancers, and 65.5% of patients had metastatic disease. In the apixaban group (n=145), no major bleeding events occurred within six months compared to three major bleeding events (2.1%) in the dalteparin group (n=142) (p=0.9956). Recurrent VTE occurred in five patients (3.4%) in the apixaban group and 20 patients (14.1%) in the dalteparin group (HR [hazard ratio]: 1.36; 95% CI [confidence interval]: 0.79-2.35). Monthly quality of life surveys regarding concern for excess bruising, stress, irritation, burden of delivery, and overall satisfaction (p<0.05) also favored apixaban. Thus, data from this trial supports oral apixaban therapy as it was associated with low rates of bleeding and significantly lower VTE recurrence rates. However, full results of this study have not been published yet.
The SELECT-D Trial was a multicenter, open-label pilot study that assessed the safety and efficacy of rivaroxaban for treatment of active VTE in patients with cancer. Patients with an active VTE were randomized to receive dalteparin or rivaroxaban (15 mg BID for three weeks, followed by 20 mg daily for a total of six months). The most prevalent primary tumors included colorectal cancer and lung cancer. The primary efficacy endpoint (VTE recurrence at 6 months) occurred in 18 (8.9%) of 203 dalteparin patients and eight (3.9%) of 203 rivaroxaban patients, resulting in a cumulate VTE recurrence rate at six months of 11% for patients receiving dalteparin and 4% for those receiving rivaroxaban (HR: 0.43; 95% CI: 0.19-0.99). The primary safety endpoint of major bleeding occurred in six patients (3.0%) receiving dalteparin and 11 patients (5.4%) receiving rivaroxaban, resulting in a cumulative major bleeding rate of 4% for the dalteparin group and 6% for rivaroxaban group (HR: 1.83; 95% CI: 0.68-4.96). Major bleeding events most commonly occurred within the gastrointestinal tract, and there were no identified CNS bleeds. Clinically relevant non-major bleeding (CRNMB) during the six-month period occurred in 4% of dalteparin patients and 13% of rivaroxaban patients (HR: 3.76; 95% CI: 1.63-8.69), indicating that although rivaroxaban and dalteparin have similar rates of major bleeding, patients receiving rivaroxaban experienced higher rates of CRNMB. Most CRNMB occurred within gastrointestinal or urologic systems. Overall, patients with esophageal/gastroesophageal cancer experienced more bleeding compared to other cancer types, which may be related to the site of action of rivaroxaban. Ultimately, this trial suggests that rivaroxaban may be a viable alternate VTE treatment option to LMWH in cancer patients. However, results of this trial cannot be translated to longer treatment due to the short follow up period.
Edoxaban: Hokusai VTE Cancer 14
The Hokusai VTE Cancer trial was an open-label, noninferiority trial that assessed the role of edoxaban for CAT treatment. Adult patients with active cancer and VTE were randomized and stratified to receive either dalteparin or edoxaban 60 mg daily after receiving a LMWH for five days. The edoxaban dose was adjusted based on renal function (CrCl 30-50 mL/min), body weight (< 60 kg), or use of concomitant potent P-glycoprotein inhibitors. Colorectal, lung, genitourinary, and breast cancer were the most common cancer types included. Patients were treated for six to 12 months as determined by the treating physician. The primary outcome (composite of recurrent VTE or major bleeding after 12 months) occurred in 67 of 522 edoxaban patients (12.8%) and 71 of 524 dalteparin patients (13.5%) (HR: 0.97; 95% CI: 0.70-1.36; p=0.006 for noninferiority; p=0.87 superiority). Separately, recurrent VTE occurred in 41 patients (7.9%) in the edoxaban group and 59 patients (11.3%) in the dalteparin group (HR: 0.71; 95% CI: 0.48-1.06; p = 0.09) while major bleeding occurred in 36 (6.9%) and 21 (4.0%) in the edoxaban and dalteparin group, respectively (HR: 1.77; 95% CI: 1.03-3.04; P = 0.04). Most major bleeding events in the edoxaban arm occurred as gastrointestinal bleeding in the setting of gastrointestinal cancer. Ultimately, edoxaban was found to be noninferior to dalteparin in regard to the primary composite outcome, but it is important to consider the patient’s risk for bleeding, particularly based on cancer type. However, the study was underpowered to determine a difference in major bleeding based on cancer site in order to determine if solely patients with gastrointestinal cancer had an increased risk of bleeding compared to other cancer types. Additionally, similar to the ADAM VTE and SELECT-D studies, the ideal duration of anticoagulation treatment remains unclear as patients received anticoagulation for up to 12 months.
Based on the available literature, rivaroxaban, edoxaban, and apixaban appear to be well-tolerated and efficacious in the treatment of CAT. However, a patient-specific approach that takes into consideration a patient’s type of cancer, renal function, hepatic function, and adherence should be utilized. A recent consensus statement from the International Society of Thrombosis and Haemostasis Scientific and Standardization Committee recommends DOACs as first-line options in cancer patients if they have a low bleeding risk, and there are no drug-drug interactions.15 Remaining patients should continue to receive LMWH, especially if they have a high risk of bleeding. In particular, DOACs appear to consistently be associated with increased bleeding risk in patients with gastrointestinal or genitourinary cancers, so DOACs should be avoided in these populations. In accordance, the NCCN guidelines caution the use of DOACs in patients with cancer and urinary or GI tract lesions, pathology, or instrumentation as noted in the SELECT-D and Hokusai VTE Cancer studies.3,13-14 At this time, it is difficult to make direct comparisons between DOACs in regard to their efficacy and safety due to the trial designs only comparing each DOAC to LMWH, but, most notably, rivaroxaban and edoxaban were found to have a statistically significant increased risk of CRNMB and major bleeding, respectively. Thus, patient specific factors, such as renal function, hepatic function, cancer type, and bleeding risk, should be considered when selection anticoagulation therapy.
VTE Prophylaxis in Ambulatory Cancer Patients
A cancer patient’s risk of CAT is strongly associated with the type of cancer. Currently, thromboprophylaxis in ambulatory cancer patients is not routinely recommended but has been considered in high risk patients, such as those with a high Khorana Risk Score (> 3 points indicates high risk). The Khorana score assess the patient’s cancer diagnosis, body mass index, and CBC. DOACs offer a convenient alternative for VTE prophylaxis to LMWH.16 Recently, apixaban and rivaroxaban have been assessed in trials to be utilized in this setting.
Apixaban: AVERT Trial17
The AVERT Trial was a placebo-controlled, double-blind trial that assessed the role of apixaban compared to placebo for thromboprophylaxis in intermediate-to-high risk (Khorana score >2) ambulatory patients with cancer and initiating chemotherapy. Patients were randomized to initiate apixaban 2.5 mg twice daily or placebo within 24 hours of chemotherapy initiation for a treatment period of 180 days. The most common types of primary cancer included gynecologic (25.8%), lymphoma (25.3%), and pancreatic (13.6%) cancers. The primary efficacy outcome (first episode of objectively documented major VTE (proximal DVT or PE) within 180 days) occurred in 12 of 288 patients (4.2%) in the apixaban group and 28 of 275 patients (10.2%) in the placebo group (HR: 0.41; 95% CI: 0.26-0.65; p<0.001), indicating a significantly lower risk of VTE in patients treated with apixaban, which was primarily driven by a lower rate of PE in the apixaban group. However, a statistically significant increase in major bleeding episodes was found in the apixaban group. Major bleeding events occurred in 10 of 288 patients (3.5%) in the apixaban group and five of 275 patients (1.8%) in the placebo group (HR: 2.0; 95% CI: 1.01-3.95; p=0.046). The major bleeding events were primarily associated with gastrointestinal bleeding, hematuria, and gynecologic bleeding with apixaban, and major bleeding most commonly occurred in patients with cancer of gastrointestinal or gynecologic nature. Overall, this trial displayed that there was no difference in survival between the apixaban and placebo groups; however, most of the patients in the trial had advanced stages of cancer. The study consisted of limited types of cancers, so it is difficult to make conclusions regarding apixaban’s safety and efficacy in other cancer types; however, most commonly, included patients had cancers that significantly increased their risk for thrombosis events. Additionally, this study had a limited population with reduced renal function, a population at an increased risk of bleeding.
Rivaroxaban: CASSINI Trial18
The CASSINI Trial was a double-blind, multi-centered, placebo-controlled trial. This study randomized patients with a solid tumor or lymphoma initiating a new cancer regimen and a Khorana score of at least two to receive rivaroxaban 10 mg or placebo daily for up to 180 days. Patients were screened every eight weeks for the development of the efficacy and safety endpoints. The most common types of primary cancer included pancreatic cancer (32.6%) and gastric/gastroesophageal junctional cancer (20.9%). Of patients with a solid tumor, 54.5% had metastatic disease. Of note, more patients with a history of VTE were randomly assigned to the rivaroxaban group compared to the placebo group (2.6% v. 0.5%). Additionally, 43.7% of patients in the rivaroxaban group and 50.2% of patients in the placebo group discontinued therapy prematurely. The mean intervention period (time period from the first dose of either drug through the last dose plus two days) was 4.3 months. The primary efficacy endpoint (development of DVT or PE) occurred in 11 (2.6%) of 420 rivaroxaban patients compared to 27 (6.4%) of 421 placebo patients during the intervention period (HR: 0.40; 95% CI: 0.20-0.80). However, during the period up to day 180, the primary efficacy composite endpoint occurred in 25 (6.0%) of the rivaroxaban patients compared to 37 (8.8%) of the 421 placebo patients (HR: 0.66; 95% CI: 0.40-1.09). The primary safety endpoint (major bleeding) occurred in 8 (2.0%) of the 405 rivaroxaban patients and 4 (1.0%) patients in the placebo arm (HR: 1.96; 95% CI: 0.59-6.49; p=0.26). Ultimately, in this population, low-dose rivaroxaban did not result in a statistically significant reduction in VTE at 180 days when compared to placebo, but, in the pre-specified intervention period, there was a 3.6% absolute reduction in thromboembolism with rivaroxaban, which may be hypothesis generating as this time period could be subject to bias. These findings are consistent with results of previous trials assessing rivaroxaban for thromboprophylaxis in cancer patients, such as the PROTECHT and SAVE-ONCO trials. However, the CASSINI trial included a higher-risk population. Additionally, an overall discontinuation rate of approximately 47% may be a limitation due to the inability to fully depict the bleeding and VTE occurrence. Overall, the role of rivaroxaban as thromboprophylaxis in this patient population remains promising.
Apixaban and rivaroxaban have both been shown to be noninferior to current standard therapy placebo. Current recommendation for anticoagulation therapy for ambulating cancer patients suggest that no further anticoagulation is needed. However, these studies show that DOACs may be used as primary prophylaxis in high-risk patients. Most notably, both studies showed an increased risk of bleeding, which must be considered and evaluated for each patient. Further research is needed in order to determine optimal anticoagulation in ambulating cancer patients with less advanced stages of cancer. Additionally, the optimal timing and duration of thromboprophylaxis as well as the impact of thromboprophylaxis on cancer prognosis remain unclear.
Authors: Nicholas Pauley, PharmD Candidate 2020 and
Mallory Crain, PharmD
Acute myeloid leukemia (AML) is the most common form of acute leukemia in adults.1 The average age at diagnosis is 69 years with a 5-year survival rate of 28.3%.2 A key determinant for increased survival is the patient’s ability to undergo intense induction chemotherapeutic regimens. However, intensive therapies are not always an option since some patients are unable to tolerate these treatments due to age and comorbidities. Fortunately, targeted therapies have expanded treatment options for these patients.
Targeting specific genetic mutations in AML has become a large area of research in recent years. Specifically, isocitrate dehydrogenase (IDH) 1 or 2 mutations are present in approximately 20% (IDH1: 7-14%, IDH2: 8-19%) of newly diagnosed patients with AML.3 Until recently, there were no specific therapies for patients with these mutations. Two IDH inhibitors, enasidenib and ivosidenib, were FDA approved in August 2017 and July 2018, respectively. Both agents increase myeloid differentiation through inhibition of the IDH enzymes.4,5
Enasidenib is currently FDA approved at a dose of 100 mg by mouth once daily for the treatment of relapsed/refractory AML in patients with an IDH2 mutation.4 Although enasidenib is only FDA approved for relapsed/refractory patients, the NCCN guidelines also recommend enasidenib as an option for older patients who are unfit for intensive therapy.6 No significant drug interactions requiring dose adjustments have been identified.4
A phase 1, dose escalation and expansion study evaluated AML patients with an IDH2 mutation who were treated with enasidenib. A total of 109 patients in the study had relapsed/refractory AML. The median age was 67 years, and most patients received at least two prior therapies. The overall response rate (ORR) was 38.5% with a complete remission (CR) of 20.2%. The median overall survival (OS) was 9.3 months. Of note, the median time to first response was 1.9 months.7 This study also evaluated 29 newly diagnosed patients who were deemed unfit for standard regimens. The ORR was 30.8% with a CR of 18%. The estimated median OS was 11.3 months.8
Ivosidenib is FDA approved at a dose of 500 mg for patients with an IDH1 mutation who have relapsed/refractory AML or are > 75 years with newly diagnosed AML (or those who cannot tolerate intensive induction chemotherapy). Dose adjustments for ivosidenib are recommended if it is given with strong CYP3A4 inhibitors since ivosidenib is a major CYP3A4 substrate. Induction of CYP3A4 has also been reported.5
A phase 1, dose escalation and expansion study evaluated AML patients with an IDH1 mutation who were treated with ivosidenib. A total of 179 patients had relapsed/refractory AML with a median age of 68 years. The ORR was 41.6% with a CR of 21.6%. The median OS in the primary efficacy group was 8.8 months. Similar to enasidenib, the median time to response was 1.9 months. This study also included 34 patients with untreated AML (median age: 76.5 years). The ORR was 58.8% with a CR of 26.5%. Survival data was not published for these patients.9
In regard to safety, both agents have a similar adverse effect profile. The most common adverse events observed in clinical trials were diarrhea, nausea, leukocytosis, febrile neutropenia, and anemia. In addition, 38% of patients treated with enasidenib had indirect hyperbilirubinemia, and 24.6% of patients who received ivosidenib had a prolonged QTc interval. Both agents caused differentiation syndrome in approximately 5% of patients, which is a serious complication that can become life-threatening. Therefore, it is imperative that clinicians are able to identify and treat differentiation syndrome when it occurs.7,10,13
Differentiation syndrome results from rapid proliferation and differentiation of myeloid cells leading to cytokine imbalance and inflammation throughout the body. It can present as a fever, cough, dyspnea, hypoxia, pleural effusions, pulmonary infiltrates, or organ dysfunction of unknown cause. The median onset was 29 days (range 5 to 59) for ivosidenib and 48 days (range 10 to 340) for enasidenib in the phase 1 trials.7,9 Patients who experience differentiation syndrome should be initiated on dexamethasone 10 mg IV every 12 hours for a minimum of 3 days or until symptoms resolve. If patients also develop leukocytosis, initiation of hydroxyurea may be considered. Ivosidenib and enasidenib should only be discontinued if severe symptoms persist for more than 48 hours after the start of dexamethasone.4,5
Within recent years, several new agents, including targeted therapy, have emerged as treatment options for AML. In a disease state with previously limited options, having additional lines of therapy potentially allows for increased survival compared to historical treatment options. While intensive induction therapy is still the standard of care for those who can tolerate it, it is not an option for every patient. IDH inhibitors provide another treatment option for relapsed/refractory AML patients as well as those who cannot tolerate intensive induction therapy. In addition, an oral medication taken at home may be more convenient or desirable for some patients. When comparing these agents to traditional chemotherapy, one important factor to consider is the longer expected time to response. The median time to response with IDH inhibitors is 1.9 months compared to an expected response within 30 days with traditional chemotherapy. Although long-term efficacy data is not yet available, the IDH inhibitor phase 1 trials show similar results compared to other standard treatment options given in the relapsed/refractory and newly diagnosed settings.6-9,11 Overall, both of these agents have proven efficacy in AML patients with an IDH mutation, and it is likely that use of IDH inhibitors for the treatment of AML will only continue to grow.
Authors: Avatar Patel, PharmD Candidate 2020; Marissa Olson, PharmD, BCOP and Kristan Augustin, PharmD, BCOP
Cytomegalovirus (CMV) is the largest β-herpesvirus transmitted by direct contact with infectious body fluids and is prevalent in over half of adults by the age of 40 years.1 CMV infection and disease are often characterized together, although they are not synonymous. CMV infection refers to the detection of viral antigens in tested bodily fluid or tissue, while CMV disease refers to symptomatic end-organ disease.2 While most individuals do not have signs or symptoms associated with CMV infection, primary infection leads to life-long latency. Reactivation of CMV infection occurs in 50-60% of patients after hematopoietic stem cell transplantation (HSCT) due to decreased CD4+ and CD8+ lymphocytes and represents the most common infection in HSCT.2 CMV reactivation is associated with increased morbidity and mortality post-HSCT. Common complications include pneumonia, colitis, and hepatitis. Risks for CMV reactivation include recipient and donor CMV seropositivity, transplant modality, and recipient’s age. Infection risk in HSCT patients can be broken down into three phases which include early phase (day 0 to day 30), intermediate phase (day 31 to day 100), and late phase (day 101 and after) post-transplant. Although CMV reactivation in HSCT patients can occur at any time, most reactivation is seen during the intermediate phase. Without prophylaxis, 80% of CMV-seropositive patients undergoing HSCT will have CMV reactivation.4
Prevention of CMV complications in HSCT patients can be approached by primary prophylaxis or preemptive therapy. Primary prophylaxis includes treating high risk patients, defined as recipients who are CMV-seropositive, during the first 100 days after transplant. Preemptive therapy is defined as the initiation of therapy after the detection of CMV viremia. Current National Comprehensive Cancer Network (NCCN) guidelines for preemptive therapy recommend valganciclovir or ganciclovir as first-line agents for the treatment of CMV viremia. Foscarnet or cidofovir are recommended as second-line agents for resistant CMV or for patients unable to tolerate first line therapy.5 The major limitations of preemptive therapy include weekly clinical follow-up and lack of protection against early CMV reactivation, which can lead to complications. While primary prophylaxis reduces early CMV reactivation, it does not prevent late onset reactivation, and use of antiviral therapies may be associated with significant adverse events such as myelosuppression and nephrotoxicity.6
Letermovir (PrevymisTM) was approved by the Food and Drug Administration (FDA) in November 2017 for CMV prophylaxis in HSCT CMV-seropositive recipients. Letermovir is the first non-nucleoside 3,4 dihydroquinazoline, reversible viral terminase inhibitor. It acts on the late stages of viral replication by inhibiting viral terminase at UL56 subunit which prevents viral DNA cleavage and results in inhibition of viral replication.6 Letermovir differs from other antiviral agents with CMV activity, such as ganciclovir, valganciclovir and foscarnet, in that it does not target UL54. Rather, it has a unique binding domain on UL56, which prevents cross-resistance with other agents.5 It is available as both an immediate-release tablet and intravenous formulation. It is initiated at 480 mg once daily beginning between day 0 and day 28 posttransplant and continued through day 100. Letermovir is eliminated via hepatic uptake OATP1B1/3 with a half-life of 12 hours.
In addition, letermovir is also a substrate of P-glycoprotein and a moderate inhibitor of CYP3A and CYP2C8 which can lead to drug-drug interactions. Trials have shown letermovir reduces the AUC of voriconazole by 50% and increases the AUC and Tmax of atorvastatin.2 Dosage should be decreased to 240 mg once daily in patients receiving concomitant therapy with cyclosporine as cyclosporine-mediated OTAP1B1/3 inhibition has been shown to double the AUC of letermovir.7 There are no dose adjustments recommended for creatinine clearance > 10 ml/min and mild or moderate hepatic impairment (Child Pugh class A or B). Letermovir is also not recommended in patients with severe hepatic impairment (Child Pugh class C) due to increased exposure.
NCCN guidelines updated in early 2019 added letermovir as a first-line agent for CMV prophylaxis in CMV-seropositive allogeneic HSCT recipients based on the results of a phase III study. The trial randomized 545 subjects in a 2:1 ratio to receive letermovir or placebo daily through week 14. The primary end point was the proportion of subjects with clinically significant CMV infection, defined as > 300 copies/ml via PCR testing, through week 24. Patients were stratified based on CMV disease risk and were eligible if they were CMV-seropositive and had an undetectable level of CMV DNA within 5 days of randomization. A decrease in clinically significant CMV infection at week 24 was observed in the letermovir group compared to the placebo group (37.5% vs. 60.6%, p < 0.001). In addition, all-cause mortality was lower at week 24 for patients receiving letermovir (10.2% vs. 15.9%, p < 0.03). Patients being treated for graft versus host disease (GvHD) or those with T-cell depleted grafts were found to have the greatest benefit from letermovir prophylaxis. However, the trial did show a rise in CMV infection when letermovir was discontinued after 100 days which may suggest the reduced benefit of letermovir prophylaxis when discontinued. There were no statistical significant differences in adverse effects between the two treatment groups.7
Letermovir has proven efficacy when used as CMV prophylaxis in HSCT CMV-seropositive recipients. It offers clinicians a therapeutic option without the significant toxicities seen with other antiviral treatments. Although the phase III trial showed a significant decline in rates of CMV infection and all-cause mortality at 24 weeks, there are still unanswered questions. Upon discontinuation of letermovir, high risk patients were more likely to have CMV reactivation. In addition, while this trial only evaluated letermovir for prevention of CMV in HSCT patients, future trials may assess the potential option to use letermovir as a treatment option due to the minimal adverse effect profile.
1. Centers for Disease Control and Prevention. Cytomegalovirus (CMV) and Congenital CMV Infection. www.cdc.gov/cmv/overview (accessed 2019 June 6).
2. Ljungman P, Boeckh M, Hirsch HH et al. Definitions of Cytomegalovirus infection and disease in transplant patients for use in clinical trials. Clin Infect Dis. 2016;1(1):87-91.
3. Deleenheer B, Spriet I, Maertens J. Pharmacokinetic drug evaluation of letermovir prophylaxis for cytomegalovirus in hematopoietic stem cell transplantation. Expert Opinion on Drug Metabolism & Toxicology. 2018;14(12):1197-1207.
4. Styczynski J. Who is the patient at risk of CMV recurrence: A review of the current scientific evidence with a focus on hematopoietic cell transplantation. Infect Dis Ther. 2018;7:1-16.
5. National Comprehensive Cancer Network. Prevention and treatment of cancer-related infections (updated 2019). www.nccn.org/professionals/physician_gls/pdf/infections.pdf (accessed 2019 Jul 18).
6. Razonable RR. Role of letermovir for prevention of cytomegalovirus infection after allogeneic hematopoietic stem cell transplantation. Curr Opin Infect Dis. 2018;31:286-291.
7. Foolad F, Aitken SL, Chemaly RF. Letermovir for the prevention of cytomegalovirus infection in adult cytomegalovirus-seropositive hematopoietic stem cell transplant recipients. Expert Review of Clinical Pharmacology. 2018;11(10):931-941.
Authors: Betsy Abraham, PharmD: PGY-1 Pharmacy Resident, NorthShore University HealthSystemKatie Lentz, PharmD, BCOP: Oncology Clinical Pharmacy Specialist, Barnes-Jewish Hospital
Nausea and vomiting are common in patients who are on chemotherapy. A recent analysis of 991 patients receiving chemotherapy showed an incidence of anticipatory nausea of 8 to 14%, with rates increasing with each subsequent cycle.1 Patients beginning a cancer treatment consistently list chemotherapy-induced nausea and vomiting (CINV) as one of their greatest fears.2 Patient factors which increase the risk of nausea and vomiting include: female gender, age less than 50 years, dehydration, history of motion sickness, prior history of nausea and vomiting with chemotherapeutic agents, receiving chemotherapy outpatient, dose and emetogenicity of chemotherapy, no history of alcohol consumption and radiation (whole body or upper abdomen). Inadequately controlled emesis decreases the quality of life for patients, increases the use of healthcare resources, and can impair a patient from completing chemotherapy.3-4 However, new insights into the pathophysiology of CINV and a better understanding of the risk for these effects have helped clinicians better treat and prevent CINV.
There are three subtypes of CINV which include: acute, delayed and anticipatory (see Table 1 for list of available agents). Acute CINV occurs within 24 hours after chemotherapy. Patients who are at greater risk for anticipatory CINV include those who have any of the patient factors which increase the risk of nausea and vomiting. The neurotransmitter responsible for anticipatory CINV is serotonin (5HT3). Therefore, treatment of CINV is with 5HT3 receptor antagonists (5HT3-RA) such as ondansetron (Zofran®). On the other hand, delayed CINV occurs 1 to 7 days after chemotherapy. The chemotherapeutic classes/agents which increase the risk for delayed CINV are ones of high emetic risk (> 90% of patients experience CINV without appropriate prophylaxis) which include, but are not limited to: anthracyclines, platinum analogs, cyclophosphamide (Cytoxan®), and ifosfamide (Ifex®).5 The neurotransmitter believed to primarily be responsible for delayed CINV is Substance P. However, delayed CINV is treated with a combination of antiemetics which include Neurokinin-1 receptor antagonists (NK1-RA) such as aprepitant (Emend®) and fosaprepitant intravenous (Emend®), corticosteroids, and the 5HT3-RA palonosetron (Aloxi®) (see Table 2 for list of combinations).6-7 Finally, anticipatory CINV happens prior to receiving a chemotherapeutic agent and is seen in patients with a history of CINV with prior use of chemotherapeutic agents. Treatment of anticipatory CINV is with benzodiazepines, specifically lorazepam (Ativan®).
Despite receiving antiemetic prophylaxis for acute and/or delayed CINV, some patients may experience breakthrough nausea and vomiting. Various antiemetics may be used during this time, including 5HT3-RAs, dopamine receptor antagonists, and cannabinoids. 5HT3-RAs such as ondansetron, palonosetron, granisetron (Kytril®) and dolasetron (Anzemet®) are usually well-tolerated by most patients and have constipation and migraine-like headaches as its side effects. Dopamine receptor antagonists such as prochlorperazine (Compazine®), promethazine (Phenergan®), and metoclopramide (Reglan®) are commonly prescribed; however, these agents carry unpleasant side effects such as extrapyramidal symptoms such as acute dystonia as well as sedation.6-7 Patients who develop acute dystonic reactions are treated with anticholinergics: benztropine (Cogentin®) and diphenhydramine (Benadryl®). Furthermore, cannabinoids, like dronabinol (Marinol®) and nabilone (Cesamet®) can be used second line for breakthrough CINV. These are synthetic analogs of delta-9-tetrahydrocannabinol, a naturally occurring component of Cannabis sativa. Cannabinoids carry side effects such as increased appetite, sedation, dysphoria, or euphoria. Therefore, these agents are prescribed only when patients have CINV with the preferred agents.6-8
Additionally, one agent that has recently come to prominence for CINV is the second-generation anti-psychotic olanzapine (Zyprexa®) typically used for the treatment of bipolar I disorder and schizophrenia. A randomized, double-blind phase 3 trial compared olanzapine with placebo in combination with dexamethasone (Decadron®), aprepitant or fosaprepitant, and a 5HT3-RA. The study revealed that the anti-emetic combination with olanzapine, as compared with placebo, had a lower proportion of patients with no CINV in the first 24 hours (74% vs. 45%, p = 0.002), the period from 25 to
120 hours after chemotherapy (42% vs. 25%, p = 0.002), and the overall 120-hour period (37% vs. 22%, P=0.002).9 Moreover, complete-response rate was also significantly increased with olanzapine during the three periods: 86% versus 65% (p < 0.001), 67% versus 52% (P=0.007), and 64% versus 41% (P<0.001).9 Dosed at 5-10 mg by mouth daily, olanzapine has become a novel agent used in combination with dexamethasone and palonosetron in patients with moderate to high emetogenic potential.
Authors: Justice Oehlert, PharmD Candidate 2020 and
Kathryn Lincoln, PharmD, BCPS, BCIDP, Clinical Pharmacist – Infectious Diseases, Olathe Medical Center
The discovery of antibiotics in the 20th century ushered in a golden age of medicine. Before the discovery of penicillin in 1928 and its subsequent wide-spread use, bacterial infections were much more deadly. The introduction of antimicrobial therapies markedly increased the average life expectancy and drastically reduced the mortality rate of communicable diseases. Over the next several decades many new classes of antibiotics were discovered and marketed. As we entered the 21st century, the discovery of new antibiotic classes plateaued, and newly approved agents had been limited to classes that were already established. Bacterial resistance to antibiotics has steadily followed the introduction of new agents. As soon as an agent is used in clinical practice, populations of bacteria that are exposed begin selecting individuals that harbor genetic mechanisms of resistance. Furthermore, resistance mechanisms often render the pathogen resistant to multiple, if not all, agents in a given class of antibiotics. Due to the costly development process and low rate of return on investment, pharmaceutical companies have had little incentive to perform research and development on new antimicrobial agents. Thus, we are currently seeing higher rates of resistance to our commonly employed antibiotics. Agents that had typically been reserved due to toxicity or low resistance, such as colistin, tigecycline or carbapenems, are being forcibly employed. As a result, resistance to these agents is increasing at an alarming rate. Pairing this resistance with a lack of viable antibiotic treatment options leads to a global crisis. The 2014 study commissioned by the UK government used predictive modeling to demonstrate that, in a worst case scenario, by 2050, the death rate from resistant bacteria could be as high as 10 million individuals per year, surpassing the current death rate of cancer.1
Pathogenic bacteria in humans are acquiring resistance at an alarming rate, often to many different available antibiotics. Multi-drug resistant (MDR) bacteria are non-susceptible to at least one agent in three or more antimicrobial classes, extensively-drug resistant (XDR) are non-susceptible to at least one agent in all but two or fewer classes, and pandrug-resistant bacteria are non-susceptible to all available agents.2 Some of the most concerning organisms to consider are gram negative bacilli (GNB), which are responsible for 45-70% of ventilator-associated pneumonia cases (VAP), 20-30% of catheter-related bloodstream infections, and commonly cause sepsis related to urinary tract infections (UTI) or surgical site infections.3 Gram-negative bacteria are often intrinsically more resistant to common antibiotics due to their additional lipopolysaccharide membrane, which serves as a permeability barrier to many drugs.2 Additionally, gram-negative bacteria can acquire resistance through mutations as well as horizontally transfer resistance genes through transformation, transduction, and conjugation both within and between species. Bacteria introduced into humans via consumption of livestock is potentially able to transfer resistance, having been demonstrated with extended spectrum beta-lactamase (ESBL) and the colistin resistance gene mcr-1 in GNR.2
The most relevant MDR gram-negative pathogens in humans are members of Enterobacteriaceae, such as Escherichia coli, Citrobacter spp., Enterobacter spp., Klebsiella spp., Pseudomonas aeruginosa, and Acinetobacter spp. In the latest antibiotic resistance report released by the CDC in 2013, carbapenem-resistant Enterobacteriaceae (CRE) account for approximately 9,000 infections and 600 deaths per year.10
Several studies have been performed to evaluate resistance rates of GNB in institutional settings. The INICC, SENTRY, ANSRPRG, and EARS-NET analyzed data in a multitude of countries and in both ICU and non-ICU settings. Results demonstrated Enterobacteriaceae resistance to fluoroquinolones from 0-70%, 3rd generation cephalosporins 0-72%, and carbapenems 0-59%, depending on the study. Pseudomonas aeruginosa was 0-53% resistant to fluoroquinolones, 0-51% resistant to aminoglycosides, 0-55% resistant to piperacillin/tazobactam, 0-44% resistant to ceftazidime, and 3-60% resistant to carbapenems. The resistance variability between study sites reiterates the importance of generating local antibiograms to help guide empiric therapy for bacterial infections.
For Enterobacteriaceae, the primary mechanism of resistance to beta-lactams is the production of beta-lactamases, which are enzymes that hydrolyze the beta-lactam ring of these agents and render them unable to bind to penicillin-binding protein (PBP). Additionally, AmpC, an inducible beta-lactamase, can confer further resistance to 2nd and 3rd generation cephalosporins in Enterobacter spp., Citrobacter freundii, Serratia marcescens, Morganella morganii, and others. Exposure to penicillins and 1st-3rd generation cephalosporins can cause the AmpC gene to become de-repressed and resistance can evolve quickly. Additionally, plasmid-borne beta-lactamases of the ESBL variety confer resistance to all cephalosporins. Finally, strains which carry plasmid-borne carbapenemases that inactivate carbapenems have rapidly spread.3
While all Enterobacteriaceae are naturally susceptible to fluoroquinolones, chromosomal mutations in DNA gyrase and topoisomerase IV genes modify the binding affinity and raise the MIC for specific agents. Additionally, mutations may lead to decreased permeability into the cytoplasm or increased drug efflux. Plasmid-borne mechanisms of resistance have also been observed, and are frequently associated with ESBL producing strains.3
Pseudomonas aeruginosa, like the Enterobacteriaceae, also carry an inducible AmpC cephalosporinase that confer resistance to 3rd generation cephalosporins. Wild-type strains are intrinsically resistant to amoxicillin, amoxicillin/clavulanate, 1st and 2nd generation cephalosporins, cefotaxime, ceftriaxone, and ertapenem. They are susceptible to piperacillin, ceftazidime, cefepime, imipenem, meropenem, and doripenem. Mutations in efflux transporters rendering them overexpressed confers resistance to aztreonam, cefepime, and meropenem. Fluoroquinolone resistance results from mutations in topoisomerase-encoding genes and/or hyperactive efflux systems. Finally, colistin resistance has been well documented in regards to selection of mutants. More recently, transferable resistance has been described in Pseudomonas harboring mcr-5, a variant of the gene discussed previously.3,11
The newest advancement in the bacterial arms race is the emergence of resistance to colistin. Certain species are intrinsically resistant, such as Proteus spp., Providencia spp., Serratia spp., and Morganella spp. Naturally, MDR strains of these organisms are concerning due to the lack of susceptibility to colistin, which is currently the last resort agent for CRE. Until recently, transferable resistance to colistin had not been observed. The plasmid-borne mcr-1 gene confers resistance to colistin and was described in farm animals in several countries, including the U.S. In China, the mcr-1 gene has been found in humans, livestock, and food products.2,3
Ceftolozane/tazobactam (TOL/TAZ) is a cephalosporin/beta-lactamase inhibitor combination FDA approved for the treatment of complicated intra-abdominal infections (cIAIs), in combination with metronidazole, and complicated urinary tract infections (cUTIs), including pyelonephritis. TOL/TAZ demonstrated superiority to levofloxacin in the outcomes of composite cure and microbiological eradication in cUTI. It was non-inferior to meropenem in the outcome of clinical cure of cIAI.5 It is highly potent against P. aeruginosa, most Enterobacteriaceae and also ESBL-producing GNB, but provides little activity against Acinetobacter baumannii.5,7 Common mechanisms of resistance in P. aeruginosa are ineffective against ceftolozane/tazobactam. TOL/TAZ provides most of its utility in practice towards treating Pseudomonas and ESBL producing GNB infections while sparing carbapenems. It has been referred to as the most potent antibiotic against Pseudomonas.7
Ceftazidime/avibactam (TAZ/AVI) is a cephalosporin/beta-lactamase inhibitor combination FDA approved for cUTI, cIAI (in combination with metronidazole), healthcare-associated pneumonia (HAP) and VAP.7 The addition of avibactam restores activity of ceftazidime to a variety of organisms, including ESBL producing GNB and some, but not all, carbapenemase producing GNB, including Pseudomonas aeruginosa.4,5,7 In comparison to TOL/TAZ, the presence of avibactam leads to retention of activity against GNB that produce Klebsiella pneumoniae carbapenemases (KPC).6 In clinical trials, TAZ/AVI plus metronidazole was compared with meropenem in patients with cIAIs and nosocomial pneumonia, and proved non-inferiority. An open-label trial comparing TAZ/AVI to best available therapy in cUTI or cIAI caused by ceftazidime-resistant Enterobacteriaceae or P. aeruginosa showed utility as an alternative to carbapenems.7 The Consortium of Resistance Against Carbapenems in Klebsiella and other Enterobacteriaceae (CRACKLE) database demonstrated that therapy for CRE infection with TAZ/AVI had significantly lower mortality than therapy with colistin. Current data does not support the use of TAZ/AVI as monotherapy when MDR GNB are suspected. Use of local antibiograms should be employed to pair its use with an aminoglycoside, fosfomycin, tigecycline, or colistin.7
Meropenem/vaborbactam is the first carbapenem/beta-lactamase inhibitor combination product available. Addition of vaborbactam restores activity of meropenem against some, but not all, carbapenemase producing GNB.7 It was FDA approved for cUTI, including acute pyelonephritis, after demonstrating non-inferiority to piperacillin/tazobactam.4,7 On a negative note, one study found that the addition of vaborbactam did not increase in vitro activity against P. aeruginosa or Acinetobacter spp. in comparison to meropenem alone.4 Real-life clinical data is lacking at this point, which will be necessary to define its place in clinical practice.7
Plazomicin is the newest agent in the aminoglycoside class and is active against MDR Enterobacteriaceae due to its stability against AMEs.4,7 Plazomicin spectrum of activity includes Enterobacteriaceae (including CRE, ESBL, and MDR isolates) as well as methicillin-resistant Staphylococcus aureus (MRSA) irrespective of resistance to currently available aminoglycosides. Moreover, plazomicin has demonstrated favorable in vitro activity against polymyxin-resistant Enterobacteriaceae, including mcr-1 producing isolates.4,9 FDA approval was achieved for cUTI based on comparisons of plazomicin with meropenem or colistin with concurrent tigecycline or meropenem, in which non-inferiority was demonstrated. Favorable lung penetration, in comparison to colistin, may hold some promise as to future adjunctive therapy for VAP. Plazomicin potentially has utility as part of combination therapy for XDR GNB along with novel beta-lactams.7
Eravacycline, a synthetic fluorocycline with similarities to tigecycline, has activity against GNB and gram positive cocci. It inhibits peptide elongation by binding to the 30s subunit of the bacterial ribosome and inhibiting addition of amino acids to the growing peptide chain. Many mechanisms of resistance, such as ESBL production, do not affect the activity of eravacycline. While it does not inhibit P. aeruginosa, it is active against MRSA and vancomycin-resistant enterococcus (VRE). Its advantages over tigecycline include more potent in vitro activity, excellent oral bioavailability, lower potential for drug interactions, and greater activity in biofilms. Of note, it extensively concentrates in alveolar macrophages, indicating potential utility in pneumonias caused by MDR bacteria. It is the most potent antibiotic against carbapenem resistant A. baumannii. Eravacycline is FDA approved for cIAI based on 2 clinical trials that demonstrated non-inferiority to ertapenem and meropenem.
Omadacycline is a semisynthetic derivative of minocycline within the tetracycline class. It is FDA approved for the treatment of acute bacterial skin and skin structure infections (ABSSSIs) as well as community-acquired pneumonia (CAP). Coverage includes gram-positive, including MRSA and VRE, gram-negative, anaerobic and atypical pathogens. FDA approval was obtained for ABSSSIs based on the results of 2 trials demonstrating non-inferiority to linezolid. Approval for CAP was obtained based on a trial comparing omadacycline to moxifloxacin, in which omadacycline demonstrated non-inferiority.8
Imipenem/cilastatin/relebactam (IMI/REL) is a carbapenem/beta-lactamase inhibitor that gained FDA approval in July 2019 for complicated UTIs, including pyelonephritis, and cIAIs, both due to a set of susceptible organisms. The addition of relebactam restores activity against KPC type carbapenemases, but not the other carbapenemases. IMI/REL was compared to imipenem alone in patients with cIAIs and cUTIs and demonstrated non-inferiority, but the trials were not selective for MDR infections. It is expected that IMI/REL will provide an additional therapeutic option against KPC producing GNB.4 In vitro analysis show that 32% of imipenem non-susceptible P. aeruginosa strains from the Study for Monitoring Antimicrobial Resistance Trends (SMART) global surveillance program remain resistant with the addition of relebactam.12 A trial comparing IMI/REL to piperacillin/tazobactam in patients with pneumonia has been completed, but the results are not currently available.
Ruppé E. Ann. Intensive Care. 2015; 5:21.
Submit for CE
Author: Christopher Clayton, PharmDPreceptor: Jacob Kettle, PharmD, BCOP
The human immune system possesses essential and sophisticated mechanisms capable of recognizing, attacking, and ultimately causing lysis of tumor cells.1,2 The efficacy of these processes is unfortunately limited due to insufficient numbers of T-cells specific for tumor antigens, blunted T-cell activation resulting from immune checkpoints, and an immunosuppressive tumor microenvironment.3 The principle theory behind CAR-T (chimeric antigen receptor T-cell) therapy is to overcome the shortcomings of the human immune system through the laboratory design and development of immune cells which specifically target cancer in sufficient abundance to yield a tumor response.4
CAR-T therapy is produced through a complex manufacturing process that generally takes several weeks to complete. The process begins with T-cell extraction from the patient through leukapheresis. A CAR is then introduced ex vivo to the T-cells via viral transfer vector.3,5 The CAR T-cells then undergo expansion to produce enough cells to provide an adequate dose before they can be administered to the patient. Following administration, the modified T-cells will presumably recognize the target on tumor cells and initiate an immune cascade to destroy the malignant cells.3,6,7 Due to the length of time needed to both develop a therapy and for the immune system to illicit a response after administration, the use of conventional cytotoxic chemotherapy is a necessary component of CAR-T therapy.5
Access to CAR-T is currently limited to a relatively small number of institutions owing to the complexity of CAR T-cell manufacture and administration. Further, the immense financial burden (up to $475,000 for the drug cost alone) creates additional logistical barriers to implementation.
Overview of Evidence
While CAR-T only has FDA approval for DLBCL and ALL, researchers are actively striving to identify more uses for CARs in other types of malignancy as research is underway in numerous solid tumors and hematological malignancies.14,15,16 For instance, CARs have been designed to target B-cell maturation antigen (BCMA) for treatment of multiple myeloma, type 1 insulin-like growth factor receptor (IGF1R) and receptor tyrosine kinase-like orphan receptor (ROR1) for sarcoma, and the L1-cell adhesion molecule (L1-CAM) for ovarian cancer.14,15 The greatest challenge in developing new therapy appears to be establishing targets on the cancer cells that are not routinely expressed on normal tissue.14
Treatment with CAR-T is associated with considerable risks. The most common serious complication of CAR-T therapy is cytokine release syndrome (CRS), a phenomenon caused by the rapid release of inflammatory cytokines and chemokines.17 CRS generally occurs 2-3 days following administration and is characterized by fever, hypotension, hypoxia, tachycardia, and cardiac, renal, or hepatic dysfunction.16 Reported frequency of CRS ranges from 57% to 93% of patients with many experiencing a severe and potentially life-threatening reaction.10,11,13 Management of CRS revolves around initiation of immune suppression (i.e. corticosteroids) and supportive care measures to support end organ function.16 Tocilizumab, an anti-IL-6 monoclonal antibody, is also an effective component of proper management.17,18 Beyond CRS, neurotoxicity is also a common and severe adverse effect of CAR-T. As many as 40% of patients will experience neurologic symptoms, including encephalopathy, headache, tremor, dizziness, aphasia, delirium, insomnia, anxiety, autonomic neuropathy, agitation, and psychosis.13,17 Symptoms tend to occur 4-10 days following treatment and persist for up to two weeks or longer.13,17 Seizures and life-threatening cerebral edema may also occur.17 Likewise, it is recommended to initiate one month of seizure prophylaxis beginning on the day of treatment.17 Less severe and more persistent chronic side effects of CAR-T therapy include infections, blood dyscrasias, acute kidney injury, and increased hepatic enzyme levels among others.6,7 Many of these effects could occur for up to 8 weeks following treatment.
CAR-T therapy has demonstrated efficacy in the treatment of patients with relapsed or refractory DLBCL or ALL, both of which are historically challenging disease states. Further, the potential for customization suggests CAR-T may become an important treatment modality in additional tumor types in the future. Despite the promise, CAR-T is associated with frequent and potentially life-threatening adverse events as well as financial and logistical barriers due to the complexity of this type of therapy. Assuming the current trajectory holds and use of CAR-T becomes more widespread in the future, it will become increasingly more important for pharmacists in all practice settings to become familiar with this emerging cancer treatment.
Authors: Borden Edgar, UMKC PharmD Candidate 2019 and
Sarah Cox, PharmD, MS
Medicinal marijuana is a growing topic being discussed in Missouri. Recently, Missouri passed Amendment 2, which enacted a new section to be known as Section 1 of Article XVI of the Missouri Constitution1. This change allowed the use of medical marijuana for certain medical conditions. However, marijuana is classified as a schedule I controlled substance by the Drug Enforcement Agency (DEA)2. This may pose a challenge to health-systems when caring for patients licensed and legally using medical marijuana under state law. According to the Missouri Department of Health and Senior Services (DHSS), patients could begin applying to receive a medical marijuana card on the 28th of June. For an additional $100 fee, a patient may grow up to six flowering plants1.
With the foreseeable increase in the use of medical marijuana and its derivatives, hospitals must be prepared for managing these patients and pharmacy must be at the forefront of these decisions. Fortunately, many states have legalized the use of medical marijuana and have shared recommendations or guidance for health-system policies. Minnesota and Washington were among the first to pilot successful policy guidelines with other states following similar principles3-6. In addition, the Missouri Hospital Association (MHA) recently released model medical marijuana staff bylaws and policy templates7. A description of each policy guideline is provided below.
Medical marijuana was passed in the state of Minnesota in 2014. The Minnesota Hospital Association released a recommendation for policies that gave three options for pharmacies to consider when creating their own policy.
The Missouri Hospital Association model medical marijuana staff bylaws and policy templates closely resembled the previously discussed policies provided by the Minnesota Hospital Association. The policy templates and model medical staff bylaws can be found at the following link: https://web.mhanet.com/medical-marijuana.aspx7.
Washington state legalized medical marijuana in 1998. The Washington Health Care Association released model guidelines for the recommendation of medical marijuana in long term care settings. The recommendation is for medical marijuana to be allowed but for it to be handled by the patient. The facility should verify that the patient has all required documentation and has brought their own legitimate supply of medical marijuana. The patient is then responsible for identifying a designated provider that is not affiliated with the long-term care facility. Each patient can only identify one provider and each provider can only assist one patient. This provider is responsible for checking in with the medical marijuana, dispensing it to the patient, and checking out with any leftover medical marijuana6.
Since the legalization of medical marijuana in Missouri, many health-systems have been discussing policies and procedures to put in place. And many health-systems have looked to pharmacy for the answer. Use these guidelines as blueprints to be tweaked based on individual health-system need.
Authors: Peggy Pace, RPh, BCGP, BCPS and
Chelsea Meczkowski, PharmD
Christian Hospital- St. Louis
HMG CoA reductase inhibitors, or “statins”, soon became the mainstay of treatment for secondary prevention in atherosclerotic cardiovascular disease (ASCVD) after their introduction to the prescription market in 1987. Their benefit has been primarily attributed to the reduction of blood cholesterol, specifically the LDL-C component, though other mechanisms have been proposed and are being investigated.1 After the publication in 2008 of Justification for the Use of Statins in Primary Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER), primary prevention was added as an indication for the first time.2
As the US population ages, statin use is expected to increase among elders. In fact, from 1999-2011, statin use in patients older than 80 years increased nearly four-fold.3 This article will evaluate current evidence on the safety and effectiveness of these agents in patients > 75 years when used for primary prevention. Their use for secondary prevention will not be evaluated.
There are several tools available online to estimate risk of ASCVD in patients without known heart or vascular disease. Commonly used tools are the ACC/AHA ASCVD Risk Estimator Plus and the Pooled Cohort Equations to estimate 10-year risk for ASCVD events.4,5 The outcome of these estimators is heavily dependent on age, such that all patients > 75 are advised to start statin therapy if LDL-C is 70 mg/dL or greater. A caveat is that these tools should not be used to seek therapy advice for patients older than 79 years. The American Board of Internal Medicine acknowledges these estimators’ weakness for use in the elderly with advice at “Choosing Wisely”, a campaign aimed at reduction of medication, testing, and procedure overuse. The advice to older patients states in part: “Many older adults have high cholesterol. Their doctors usually prescribe statins to prevent heart disease. But for older people, there is no clear evidence that high cholesterol leads to heart disease or death. In fact, some studies show the opposite—that older people with the lowest cholesterol levels have the highest risk of death.”6 Similarly, the American College of Cardiology 2018 Guideline on the Management of Blood Cholesterol says that for patients older than 75, statins should be started only after a clinical assessment and a discussion of risk.7 Risk for ASCVD increases with age, so why the caution when adding a statin to drug regimens of older patients?
Additions to medication regimens should be made when benefits clearly outweigh risks, and only after discussion with the patient and/or their caregiver. Reasons for caution when adding a statin include comorbidities, complicating existing drug regimens, increased expense, the potential for drug interactions with existing medications, and of course potential side effects such as myopathy, impaired cognition, and new onset diabetes.
The likelihood of drug interactions is increased in elders because the oxidative capacity of the liver decreases with age. Any medications metabolized by oxidation are more likely to accumulate.8 Statins are metabolized to varying degrees by cytochrome P450 (CYP) enzymes, an oxidative pathway.9 Medications that induce, inhibit, or compete for the CYP enzymes will require careful monitoring. These interactions could result in reduced levels/ineffectiveness (i.e., atorvastatin + rifampin) or increased levels/side effects (i.e., simvastatin + verapamil) of the statin.10,11
Myopathy, a known side effect of statin therapy, can lead to sedentary behavior resulting in increased frailty and falls. This side effect is hotly debated among experts but remains a complaint in about 1 in 5 patients.12 Avoiding movement due to muscle pain can worsen frailty and lead to weakness. A fall can be disastrous in an elder, especially if it results in a fracture requiring surgery. In addition to surgical risks, post-op complications, delayed healing, and months of physical therapy could result in loss of independence.
Cognitive impairment has been recognized with these agents, though the mechanism is not understood. Statins are thought to be protective of cognition in some conditions, but cause impairment in other patients.13 If it occurs, it is generally reversible with drug discontinuation.13 Cognitive side effects could easily be overlooked or attributed to something else, and elders themselves may be unwilling to report these symptoms.
The risk of new onset diabetes is increased with the use of statins.14 This may take years to manifest, so it may seem to be less of a concern in a person with a limited life expectancy. However, CDC reports that a person who has survived to age 75 in 2016 is expected to live on average another 12.3 years.15
Risk vs. Benefits: the Actual Numbers
The World Health Organization has requested that study results be reported in Absolute Risk Reduction (ARR) or Number Needed to Treat (NNT), rather than Relative Risk Reduction (RRR), as these convey a clearer picture of expected benefit.16 This has mostly been ignored, making it difficult to determine if a perceived benefit is worth the associated risks.17 Relative risk gives risk of occurrence of an event in the experimental group relative to the control group. Absolute risk tells us the number of events in the experimental group versus the number in the control group in absolute terms. The number needed to treat tells us how many patients have to receive a treatment for one patient to benefit.
For example, if the risk of developing a disease or condition is 20% and an intervention can reduce that risk to 15%, it is correct to say the intervention showed a RRR of 25% [(20%-15%)/20%], which sounds more significant than the ARR of 5% (20%-15%). The NNT is the inverse of the ARR, or 1/0.5=20 patients need to be treated for one to realize a benefit in this example.18 The more impressive sounding 20% RRR might persuade patients and providers to accept the risks associated with treatment, while the 5% ARR might not offer a benefit they think is worth those risks. For this reason, it is helpful to convert reported RRR to ARR or NNT for patients up front when discussing whether to start a new therapy.
JUPITER was said to prove the benefit of taking rosuvastatin for primary prevention, reporting a 43% reduction of risk, according to the trial authors.2 How did they arrive at these figures? In the placebo group the rate of a negative outcome was 1.36% while in the rosuvastatin group the rate was 0.77%. The ARR was 1.36%-0.77%=0.59%.2 Stated as RRR, this figure is (1.36-0.77)/1.36 or 43%.2 So the ARR is less than 1%, but the over 40% RRR was the figure the study authors chose to report, and what readers remember. The NNT in JUPITER is 1/0.0059= 170 patients for one year for one patient to realize a benefit.
Pravastatin in elderly individuals at risk of vascular disease (PROSPER), which enrolled patients aged 70-82, reported that the primary composite endpoint at 3 years (CHD-related death, nonfatal MI, and stroke) in the placebo group was 16.2% vs. 14.1% in the pravastatin group.19 This is an ARR = 2.1%, but is reported as a relative risk reduction of 13%.19 This corresponds to 48 patients treated for 3 years for one patient to realize a benefit. PROSPER was not exclusively a primary prevention trial, but analysis of the primary prevention subgroup showed no benefit with the statin.19
The Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack (ALLHAT-LLT) trial concluded there was no significant difference in outcomes when pravastatin vs. placebo was used for primary prevention in adults older than 65.20 The Third Heart Outcomes Prevention Evaluation(HOPE-3) trial also looked at statin use for primary prevention.21 Refreshingly, HOPE-3 reported the ARR and NNT in the published trial. The ARR was 1.1%, corresponding to 91 patients needing to be treated for 5.6 years for one patient to benefit.21 These stastistics are summarized in the table below.
Studies Evaluating Statin Use for Primary Prevention in the Elderly
A new study, Statin therapy for reducing events in the elderly (STAREE) is currently recruiting with an estimated study completion in 2033.22 Until then, we have precious few trials that include the elderly to assist in making decisions on whether to start or continue statins in patients over 75 with no evidence of ASCVD.
ASCVD increases with age so it seems reasonable that lipid lowering therapy provides a benefit in older adults, but this assumption does not always hold up to scrutiny. There are numerous other risk reduction strategies with proven benefit that should be considered besides reducing cholesterol, such as blood pressure control and lifestyle modifications.23 Shared decision making should be used to elicit patients’ values and goals of care to be sure therapies are aligned with expressed wishes.24 In addition, factors such as life expectancy, time to benefit, current comorbidities, costs, and risks of therapy must be included in frank discussions with patients and/or caregivers before agreeing on the best course of treatment for older adults.