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Cardiac events during treatment with proteasome inhibitor therapy for multiple myeloma
Cardio-Oncology volume 3, Article number: 4 (2017)
Proteasome inhibitors (PI) bortezomib and carfilzomib are cornerstone therapies for multiple myeloma. Higher incidence of cardiac adverse events (CAEs) has been reported in patients receiving carfilzomib. However, risk factors for cardiac toxicity remain unclear. Our objective was to evaluate the incidence of CAEs associated with PI and recognize risk factors for developing events.
This was a descriptive analysis of 96 patients with multiple myeloma who received bortezomib (n = 44) or carfilzomib (n = 52). We compared the cumulative incidence of CAEs using a log rank test. Patient-related characteristics were assessed and multivariate analysis was used to identify risk factors for developing CAEs.
PI-related CAEs occurred in 21 (22%) patients. Bortezomib-associated CAEs occurred in 7 (16%) patients while carfilzomib-associated cardiac events occurred in 14 (27%) patients. The cumulative incidence of CAEs was not significantly different between agents. Events occurred after a median of 67.5 days on PI therapy. Heart failure was the most prevalent event type. More patients receiving carfilzomib were monitored by a cardiologist. By multivariate analysis, a history of prior cardiac events and longer duration of PI therapy were identified as independent risk factors for developing CAEs.
AEs were common in patients receiving PIs. Choice of PI did not impact the cumulative incidence of CAEs. Early involvement by a cardiologist in patients at high risk for CAEs may help to mitigate the frequency and severity of CAEs.
Multiple myeloma (MM) is a clonal disorder of terminally differentiated plasma cells that accounts for approximately 13% of hematologic malignancies . Clinical features of MM include hypercalcemia, anemia, renal insufficiency, lytic bone disease and increased risk of infection. Proteasome inhibitors (PIs) have become cornerstone therapies for management of MM [2,3,4,5,6]. These agents bind to the constitutive 26S proteasome, causing accumulation of protein byproducts within plasma cells and subsequent apoptosis [7, 8]. Bortezomib is used predominately in the front line setting, while second-generation carfilzomib is used in the relapsed/refractory setting.
Cardiac toxicities associated with carfilzomib identified in earlier studies include hypertension, arrhythmia, heart failure, ischemic heart disease and cardiomyopathy [9, 10]. These carfilzomib-associated toxicities were confirmed to occur at a higher incidence compared to bortezomib in the ENDEAVOR trial . While a strong signal for cardiac toxicity has not been associated with bortezomib use, several case reports [12,13,14,15,16] have described CAEs in patients receiving this agent.
Patients with MM have a 54–74% risk of cardiovascular disease at baseline [1, 9, 10, 17]. Reasons for this increased burden include advanced age at diagnosis (median 62 years), exposure to various chemotherapies including autologous stem cell transplantation, and disease specific complications such as cardiac amyloidosis and renal insufficiency. The primary objective of this research was to identify cardiac event risk factors for patients receiving PI-based therapies for multiple myeloma.
This was a descriptive analysis of 96 consecutive MM patients receiving PI-based therapies at Vanderbilt University Medical Center from 2011 to 2014. MM disease risk was determined by conventional metaphase cytogenetic data or fluorescence in situ hybridization data according to the Mayo Stratification for Myeloma and Risk-Adapted Therapy . A line of therapy was defined as planned initial therapy in patients. For example, planned induction chemotherapy followed by autologous stem cell transplantation followed by maintenance therapy was considered one line of therapy. Estimated 10-year atherosclerotic cardiovascular disease (ASCVD) risk was calculated using the Pooled Cohort Equations; this represented their risk of myocardial infarction, coronary artery disease death, fatal or nonfatal stroke. Patients with light chain (AL) amyloidosis (biopsy proven or clinically suspected) were excluded.
Cardiac adverse events (CAEs) were evaluated only while patients were on active therapy with either carfilzomib- or bortezomib-based treatment. CAEs were graded according to the Common Terminology Criteria for Adverse Events version 4.0. Heart failure was characterized by at least 1 item in 2 out of the 3 following categories: symptoms (paroxysmal nocturnal dyspnea, shortness of breath, swelling, orthopnea, weight gain), physical findings (jugular venous distention, crackles, peripheral edema, S3 gallop), and diagnostic tests (pulmonary edema on chest radiograph, elevated B-type natriuretic peptide). Severity of heart failure events was defined as symptoms with mild to moderate activity (grade 2), symptoms at rest or with minimal exertion requiring intervention (grade 3), or life-threatening consequences requiring urgent intervention (grade 4). Acute coronary syndrome was defined as at least 2 out of 3 clinical findings of chest pain, troponin I elevation, and ischemic electrocardiographic changes. Sudden cardiac death was defined as death within 24 h of PI therapy without obvious cancer progression. Symptomatic arrhythmias included atrial fibrillation or flutter requiring treatment. Arterial and/or venous thromboembolism were determined by imaging. Pulmonary hypertension was defined as tricuspid regurgitation >3 m/s. Grade III hypertension was defined as systolic BP ≥160 mm Hg or diastolic BP ≥100 mm Hg requiring more than one drug or more intensive therapy than previously used. Grade IV hypertension was defined by life-threatening consequences (e.g. malignant hypertension, transient or permanent neurologic deficit, hypertensive crisis) requiring urgent intervention.
The primary objective was to determine risk factors for development of CAEs in patients receiving PI-based therapy. Patient-related factors were compared between patients with and without CAEs using the Wilcoxon rank-sum test for continuous variables and chi-square test for categorical variables. Cumulative incidence of CAEs was compared between bortezomib and carfilzomib using the log-rank test. Logistic regression multivariate analysis was performed to identify risk factors for developing PI-related CAEs. The variables considered in this analysis were a prior history of cardiac events, use of antithrombotic (antiplatelet or anticoagulant) medications, and cumulative number of days on therapy. For days on therapy analysis, various time intervals were tested. Six-month time intervals were selected based on confidence interval and reproducibility. A statistical significance level of .05 was used throughout. Computations were performed using the statistical package R (version 2.3.1).
A total of 96 patients received PIs with 46% (n = 44) receiving bortezomib-based therapy and 54% (n = 52) receiving carfilzomib-based therapy. All patients in the carfilzomib cohort had prior exposure to bortezomib during previous lines of therapy; however, only bortezomib-related events in the bortezomib cohort and carfilzomib-related events in the carfilzomib cohort were included in the analysis. The cut-off date for collection of follow-up data was July 2015.
PI-related CAEs occurred in 22% (n = 21) of patients. Table 1 and Fig. 1 depict baseline characteristics grouped by patients who experienced CAEs (cases, n = 21) versus those who did not (controls, n = 75). More patients in the cases group had a prior history of atrial fibrillation/flutter (14% vs 3%, P = .03) or heart failure (19% vs 0%, P < .001) than in the control group. Additionally, patients in the cases group were more likely to be taking antithrombotic (52% vs 29%, P = .05), beta blocker (52% vs 15%, P < .001), lipid-lowering (67% vs 23%, P < .001), or loop diuretic (19% vs 5%, P = .04) medications. Lastly, number of days on PI therapy was greater in patients who experienced CAEs versus those who did not (407 vs 250, P = .02).
By multivariate analysis (Table 2), every 6-month interval of PI therapy was associated with higher incidence of CAEs (HR 1.94, 95% CI 1.21–3.09, P = .006). Additionally, a history of cardiac events prior to initiation of PI therapy predisposed to treatment-emergent CAEs (HR 3.48, 95% CI 1.03–12.8, P = .045). Antithrombotic use trended towards greater likelihood of CAEs but did not reach statistical significance.
Cumulative incidence of CAEs was not significantly different between the 2 PI agents (log-rank test P = .41, Fig. 2). Bortezomib-related CAEs occurred in 7 (16%) out of 44 patients while carfilzomib-related CAEs occurred in 14 (27%) out of 52 patients. Carfilzomib users had significantly more prior lines of therapy (median, 2 vs. 0; P < .001) and were significantly more likely to be followed by a cardio-oncologist (35% vs. 11%, P = .008).
Events occurred after a median of 67.5 (range, 4–456) days on PI therapy. Grade 3 or 4 events accounted for 56% of CAEs. There were no cardiac arrests or deaths associated with PI therapy. In the setting of a cardiac event, planned PI therapy was permanently discontinued 29% of the time (43% of the time when a cardio-oncologist was involved, 21% of the time in the absence of cardiology care, P = .30). Heart failure was the most common type of CAE for both bortezomib and carfilzomib (Table 3). Four out of 13 (31%) heart failure events led to withdrawal of PI therapy. Nine out of 13 patients who developed symptomatic heart failure had preserved left ventricular ejection fraction (LVEF); 2 bortezomib users and 2 carfilzomib users experienced decline in LVEF to < 55% from previously normal LVEF.”
While the mechanism of cardiotoxicity from these agents is not entirely understood, off-target proteasome inhibition is believed to cause accumulation of misfolded proteins within cardiomyocytes . A number of in vitro and in vivo animal studies [20,21,22,23,24,25,26,27,28,29] have linked dysfunction of the ubiquitin-proteasome system to myocardial injury, cardiomyopathies, and atherosclerosis.
A high prevalence of cardiovascular disease is well-documented in the MM patient population, with 54–74% having a history of cardiac events at baseline [9, 10, 17]. However, risk factors for developing PI-related cardiotoxicity are not well established. Clarifying the risk factors for PI toxicity will allow providers to guide patient selection and facilitate risk reduction strategies.
We demonstrate that history of prior cardiac event was the most significant risk factor for developing PI-related CAEs. Specifically, a history of heart failure or atrial fibrillation/flutter was significantly more prevalent in patients who went on to develop CAEs versus those who did not. Patients who developed CAEs also had higher usage rates of antithrombotic (antiplatelet or anticoagulant), beta blocker, lipid lowering, and loop diuretic medications, which suggests a higher burden of baseline comorbidities in this group. Based on these findings, we recommend careful consideration of patients’ past medical history and preexisting cardiovascular risk factors with use of PI therapy.
Based on existing literature, we expected more CAEs in the carfilzomib cohort compared to the bortezomib cohort, especially since patients receiving carfilzomib were more heavily pretreated. Pooled safety data from 4 phase II clinical trials for carfilzomib demonstrated a 22% incidence of CAEs . In a retrospective study of 130 carfilzomib users with relapsed/refractory multiple myeloma (RRMM), 26 (20%) were hospitalized due to CAEs . Meanwhile, bortezomib-associated CAEs have been considered relatively uncommon. A meta-analysis of data from key phase II and III studies demonstrated a 2% incidence of bortezomib-associated high grade heart failure in both newly diagnosed and RRMM cohorts . Additionally, the 2 PI agents were directly compared in the ENDEAVOR trial , which again demonstrated a higher cardiac event rate with carfilzomib compared with bortezomib. It is interesting that a cardiac substudy within this trial found higher rates of hypertension, heart failure, and pulmonary hypertension in the carfilzomib group.
In our data from a “real world” clinical setting, there was not a statistically significant difference in CAEs between patients receiving carfilzomib or bortezomib. Crucially, patients treated with carfilzomib were significantly more likely to receive co-managed care from a cardio-oncologist. We propose that routine monitoring by a cardiologist may have reduced the incidence and severity of CAEs in carfilzomib users. Furthermore, much of the observed cardiotoxicity is perhaps difficult to distinguish from baseline cardiovascular dysfunction in this at-risk population. We therefore recommend co-managed care as a general strategy in all MM patients for risk reduction by way of optimizing medical therapy and controlling comorbidities.
Other important factors to consider include timing of events and types of cardiac toxicity. In phase II clinical trials for carfilzomib , 12% of patients experienced CAEs within 1 day of initial dosing, and the incidence of events did not increase in later cycles. While there were CAEs in this series occurring within days of initial dosing, multivariate analysis exposed a significant positive correlation between duration of therapy and risk of events. However, we cannot be certain that this correlation reflects a treatment effect rather than a longer observation period. In the phase II carfilzomib  and phase III ENDEAVOR trials , hypertension occurred most frequently but heart failure was most likely to cause treatment discontinuation. Similarly, we found that heart failure and hypertension comprised the majority of CAEs in both bortezomib and carfilzomib users.
The study may have been underpowered to detect a significant difference in incidence of CAEs between carfilzomib and bortezomib. Due to the retrospective design of this study, assignment to treatment drug was nonrandomized. Since carfilzomib is often reserved for relapsed/refractory MM, all patients in the carfilzomib cohort had prior exposure to bortezomib and in general were more heavily pretreated. Therefore, cumulative effects or delayed toxicity from previous agents may account for a higher rate of CAEs in the carfilzomib cohort. Finally, we could not rule out alternative etiologies of cardiac dysfunction when attributing suspected CAEs to PI therapy, particularly when concomitant agents were used.
Incidence of PI-related CAEs did not differ significantly between bortezomib and carfilzomib users; both agents were associated with substantial rates of cardiotoxicity. Prior history of cardiac events was associated with increased risk of developing PI-related CAEs. Longer duration of PI therapy correlated with greater likelihood of cardiotoxicity. Heart failure was both an important risk factor and subsequently the most prevalent type of PI-related cardiotoxicity. Close monitoring by a cardio-oncologist may reduce risk of CAEs.
Atherosclerotic cardiovascular disease
Cardiac adverse event
Left ventricular ejection fraction
Relapsed/refractory multiple myeloma
Raab MS, Podar K, Breitkreutz I, Richardson PG, Anderson KC. Multiple myeloma. Lancet (London, England). 2009;374(9686):324–39.
Kumar S, Flinn I, Richardson PG, Hari P, Callander N, Noga SJ, Stewart AK, Turturro F, Rifkin R, Wolf J, et al. Randomized, multicenter, phase 2 study (EVOLUTION) of combinations of bortezomib, dexamethasone, cyclophosphamide, and lenalidomide in previously untreated multiple myeloma. Blood. 2012;119(19):4375–82.
Rajkumar SV. Doublets, triplets, or quadruplets of novel agents in newly diagnosed myeloma? Hematol Am Soc Hematol Educ Program. 2012;2012:354–61.
Vij R, Wang M, Kaufman JL, Lonial S, Jakubowiak AJ, Stewart AK, Kukreti V, Jagannath S, McDonagh KT, Alsina M, et al. An open-label, single-arm, phase 2 (PX-171-004) study of single-agent carfilzomib in bortezomib-naive patients with relapsed and/or refractory multiple myeloma. Blood. 2012;119(24):5661–70.
Jagannath S, Vij R, Stewart AK, Trudel S, Jakubowiak AJ, Reiman T, Somlo G, Bahlis N, Lonial S, Kunkel LA, et al. An open-label single-arm pilot phase II study (PX-171-003-A0) of low-dose, single-agent carfilzomib in patients with relapsed and refractory multiple myeloma. Clin Lymphoma Myeloma Leuk. 2012;12(5):310–8.
Siegel DS, Martin T, Wang M, Vij R, Jakubowiak AJ, Lonial S, Trudel S, Kukreti V, Bahlis N, Alsina M, et al. A phase 2 study of single-agent carfilzomib (PX-171-003-A1) in patients with relapsed and refractory multiple myeloma. Blood. 2012;120(14):2817–25.
Demo SD, Kirk CJ, Aujay MA, Buchholz TJ, Dajee M, Ho MN, Jiang J, Laidig GJ, Lewis ER, Parlati F, et al. Antitumor activity of PR-171, a novel irreversible inhibitor of the proteasome. Cancer Res. 2007;67(13):6383–91.
Kuhn DJ, Chen Q, Voorhees PM, Strader JS, Shenk KD, Sun CM, Demo SD, Bennett MK, van Leeuwen FW, Chanan-Khan AA, et al. Potent activity of carfilzomib, a novel, irreversible inhibitor of the ubiquitin-proteasome pathway, against preclinical models of multiple myeloma. Blood. 2007;110(9):3281–90.
Siegel D, Martin T, Nooka A, Harvey RD, Vij R, Niesvizky R, Badros AZ, Jagannath S, McCulloch L, Rajangam K, et al. Integrated safety profile of single-agent carfilzomib: experience from 526 patients enrolled in 4 phase II clinical studies. Haematologica. 2013;98(11):1753–61.
Atrash S, Tullos A, Panozzo S, Bhutani M, Van Rhee F, Barlogie B, Usmani SZ. Cardiac complications in relapsed and refractory multiple myeloma patients treated with carfilzomib. Blood Cancer J. 2015;5:e272.
Dimopoulos MA, Moreau P, Palumbo A, Joshua D, Pour L, Hajek R, Facon T, Ludwig H, Oriol A, Goldschmidt H, et al. Carfilzomib and dexamethasone versus bortezomib and dexamethasone for patients with relapsed or refractory multiple myeloma (ENDEAVOR): a randomised, phase 3, open-label, multicentre study. Lancet Oncol. 2016;17(1):27–38.
Voortman J, Giaccone G. Severe reversible cardiac failure after bortezomib treatment combined with chemotherapy in a non-small cell lung cancer patient: a case report. BMC Cancer. 2006;6:129.
Hacihanefioglu A, Tarkun P, Gonullu E. Acute severe cardiac failure in a myeloma patient due to proteasome inhibitor bortezomib. Int J Hematol. 2008;88(2):219–22.
Bockorny M, Chakravarty S, Schulman P, Bockorny B, Bona R. Severe heart failure after bortezomib treatment in a patient with multiple myeloma: a case report and review of the literature. Acta Haematol. 2012;128(4):244–7.
Honton B, Despas F, Dumonteil N, Rouvellat C, Roussel M, Carrie D, Galinier M, Montastruc JL, Pathak A. Bortezomib and heart failure: case-report and review of the French Pharmacovigilance database. Fundam Clin Pharmacol. 2014;28(3):349–52.
Enrico O, Gabriele B, Nadia C, Sara G, Daniele V, Giulia C, Antonio S, Mario P. Unexpected cardiotoxicity in haematological bortezomib treated patients. Br J Haematol. 2007;138(3):396–7.
Li W, Garcia D, Cornell RF, Gailani D, Laubach J, Maglio ME, Richardson PG, Moslehi J. Cardiovascular and Thrombotic Complications of Novel Multiple Myeloma Therapies: A Review. JAMA Oncol 2016, Epub ahead of print.
Mikhael JR, Dingli D, Roy V, Reeder CB, Buadi FK, Hayman SR, Dispenzieri A, Fonseca R, Sher T, Kyle RA, et al. Management of newly diagnosed symptomatic multiple myeloma: updated Mayo stratification of Myeloma and risk-adapted therapy (mSMART) consensus guidelines 2013. Mayo Clin Proc. 2013;88(4):360–76.
Tannous P, Zhu H, Nemchenko A, Berry JM, Johnstone JL, Shelton JM, Miller Jr FJ, Rothermel BA, Hill JA. Intracellular protein aggregation is a proximal trigger of cardiomyocyte autophagy. Circulation. 2008;117(24):3070–8.
Wang P, Calise J, Powell K, Divald A, Powell SR. Upregulation of proteasome activity rescues cardiomyocytes following pulse treatment with a proteasome inhibitor. Am J Cardiovasc Dis. 2014;4(1):6–13.
Versari D, Herrmann J, Gossl M, Mannheim D, Sattler K, Meyer FB, Lerman LO, Lerman A. Dysregulation of the ubiquitin-proteasome system in human carotid atherosclerosis. Arterioscler Thromb Vasc Biol. 2006;26(9):2132–9.
Schlossarek S, Carrier L. The ubiquitin-proteasome system in cardiomyopathies. Curr Opin Cardiol. 2011;26(3):190–5.
Predmore JM, Wang P, Davis F, Bartolone S, Westfall MV, Dyke DB, Pagani F, Powell SR, Day SM. Ubiquitin proteasome dysfunction in human hypertrophic and dilated cardiomyopathies. Circulation. 2010;121(8):997–1004.
Tsukamoto O, Minamino T, Okada K, Shintani Y, Takashima S, Kato H, Liao Y, Okazaki H, Asai M, Hirata A, et al. Depression of proteasome activities during the progression of cardiac dysfunction in pressure-overloaded heart of mice. Biochem Biophys Res Commun. 2006;340(4):1125–33.
Weekes J, Morrison K, Mullen A, Wait R, Barton P, Dunn MJ. Hyperubiquitination of proteins in dilated cardiomyopathy. Proteomics. 2003;3(2):208–16.
Birks EJ, Latif N, Enesa K, Folkvang T, le Luong A, Sarathchandra P, Khan M, Ovaa H, Terracciano CM, Barton PJ, et al. Elevated p53 expression is associated with dysregulation of the ubiquitin-proteasome system in dilated cardiomyopathy. Cardiovasc Res. 2008;79(3):472–80.
Herrmann J, Wohlert C, Saguner AM, Flores A, Nesbitt LL, Chade A, Lerman LO, Lerman A. Primary proteasome inhibition results in cardiac dysfunction. Eur J Heart Fail. 2013;15(6):614–23.
Nowis D, Maczewski M, Mackiewicz U, Kujawa M, Ratajska A, Wieckowski MR, Wilczynski GM, Malinowska M, Bil J, Salwa P, et al. Cardiotoxicity of the anticancer therapeutic agent bortezomib. Am J Pathol. 2010;176(6):2658–68.
Tian Z, Zheng H, Li J, Li Y, Su H, Wang X. Genetically induced moderate inhibition of the proteasome in cardiomyocytes exacerbates myocardial ischemia-reperfusion injury in mice. Circ Res. 2012;111(5):532–42.
Xiao Y, Yin J, Wei J, Shang Z. Incidence and risk of cardiotoxicity associated with bortezomib in the treatment of cancer: a systematic review and meta-analysis. PLoS One. 2014;9(1):e87671.
Availability of data and materials
The dataset is available from the corresponding author on reasonable request.
RFC and DJL conceived and designed the study. JHC, RFC, and SLH collected and interpreted the retrospective data. SEP performed statistical analysis. JHC drafted the manuscript, which was revised by DJL and RFC. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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Chen, J.H., Lenihan, D.J., Phillips, S.E. et al. Cardiac events during treatment with proteasome inhibitor therapy for multiple myeloma. Cardio-Oncology 3, 4 (2017). https://doi.org/10.1186/s40959-017-0023-9
- Proteasome inhibitors
- Risk factors