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The First Autopsy Case of Fatal Acute Cardiac Failure after Administration of Carfilzomib in a Patient with Multiple Myeloma

Carfilzomib (CFZ) improves progression-free survival for patients with relapsed or refractory multiple myeloma (MM) but has shown higher frequency of cardiovascular adverse events (CVAEs) than other proteasome inhibitors. We report the first autopsy case of acute death from cardiac failure shortly a...

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Autores principales: Takakuwa, Teruhito, Otomaru, Ippei, Araki, Taku, Miura, Akiko, Fujitani, Yotaro, Mochizuki, Yasuhide, Miyagi, Yoshimi, Senzaki, Hideto, Yamamura, Ryosuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6512067/
https://www.ncbi.nlm.nih.gov/pubmed/31183224
http://dx.doi.org/10.1155/2019/1816287
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author Takakuwa, Teruhito
Otomaru, Ippei
Araki, Taku
Miura, Akiko
Fujitani, Yotaro
Mochizuki, Yasuhide
Miyagi, Yoshimi
Senzaki, Hideto
Yamamura, Ryosuke
author_facet Takakuwa, Teruhito
Otomaru, Ippei
Araki, Taku
Miura, Akiko
Fujitani, Yotaro
Mochizuki, Yasuhide
Miyagi, Yoshimi
Senzaki, Hideto
Yamamura, Ryosuke
author_sort Takakuwa, Teruhito
collection PubMed
description Carfilzomib (CFZ) improves progression-free survival for patients with relapsed or refractory multiple myeloma (MM) but has shown higher frequency of cardiovascular adverse events (CVAEs) than other proteasome inhibitors. We report the first autopsy case of acute death from cardiac failure shortly after administration of carfilzomib. A 74-year-old female was diagnosed with IgA MM after a 2-year period of smoldering MM. She was refractory to both bortezomib plus dexamethasone and lenalidomide plus dexamethasone therapies, so she subsequently received CFZ in combination with lenalidomide and dexamethasone. The day after the start of the therapy, she complained of severe dyspnea with a significant decline in left ventricular ejection fraction. Her acute cardiac failure rapidly progressed, and she died on day 7 of the start of CFZ. The autopsy showed invasion of inflammatory cells between the myocardial cells and very little myocardial necrosis. There was no obvious thrombus in the coronary artery of the heart, and no infarction or amyloid deposition was observed in the myocardium. Pathological findings of hypersensitivity myocarditis, a drug-induced cardiomyopathy, appeared to agree with this case except for absence of an eosinophilic infiltration of the myocardium. A CFZ-induced CVAE is generally considered reversible. However, rapidly progressing fatal heart failure like in our case is rare. To characterize CFZ-associated CVAE, further case collection is needed.
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spelling pubmed-65120672019-06-10 The First Autopsy Case of Fatal Acute Cardiac Failure after Administration of Carfilzomib in a Patient with Multiple Myeloma Takakuwa, Teruhito Otomaru, Ippei Araki, Taku Miura, Akiko Fujitani, Yotaro Mochizuki, Yasuhide Miyagi, Yoshimi Senzaki, Hideto Yamamura, Ryosuke Case Rep Hematol Case Report Carfilzomib (CFZ) improves progression-free survival for patients with relapsed or refractory multiple myeloma (MM) but has shown higher frequency of cardiovascular adverse events (CVAEs) than other proteasome inhibitors. We report the first autopsy case of acute death from cardiac failure shortly after administration of carfilzomib. A 74-year-old female was diagnosed with IgA MM after a 2-year period of smoldering MM. She was refractory to both bortezomib plus dexamethasone and lenalidomide plus dexamethasone therapies, so she subsequently received CFZ in combination with lenalidomide and dexamethasone. The day after the start of the therapy, she complained of severe dyspnea with a significant decline in left ventricular ejection fraction. Her acute cardiac failure rapidly progressed, and she died on day 7 of the start of CFZ. The autopsy showed invasion of inflammatory cells between the myocardial cells and very little myocardial necrosis. There was no obvious thrombus in the coronary artery of the heart, and no infarction or amyloid deposition was observed in the myocardium. Pathological findings of hypersensitivity myocarditis, a drug-induced cardiomyopathy, appeared to agree with this case except for absence of an eosinophilic infiltration of the myocardium. A CFZ-induced CVAE is generally considered reversible. However, rapidly progressing fatal heart failure like in our case is rare. To characterize CFZ-associated CVAE, further case collection is needed. Hindawi 2019-04-28 /pmc/articles/PMC6512067/ /pubmed/31183224 http://dx.doi.org/10.1155/2019/1816287 Text en Copyright © 2019 Teruhito Takakuwa et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Takakuwa, Teruhito
Otomaru, Ippei
Araki, Taku
Miura, Akiko
Fujitani, Yotaro
Mochizuki, Yasuhide
Miyagi, Yoshimi
Senzaki, Hideto
Yamamura, Ryosuke
The First Autopsy Case of Fatal Acute Cardiac Failure after Administration of Carfilzomib in a Patient with Multiple Myeloma
title The First Autopsy Case of Fatal Acute Cardiac Failure after Administration of Carfilzomib in a Patient with Multiple Myeloma
title_full The First Autopsy Case of Fatal Acute Cardiac Failure after Administration of Carfilzomib in a Patient with Multiple Myeloma
title_fullStr The First Autopsy Case of Fatal Acute Cardiac Failure after Administration of Carfilzomib in a Patient with Multiple Myeloma
title_full_unstemmed The First Autopsy Case of Fatal Acute Cardiac Failure after Administration of Carfilzomib in a Patient with Multiple Myeloma
title_short The First Autopsy Case of Fatal Acute Cardiac Failure after Administration of Carfilzomib in a Patient with Multiple Myeloma
title_sort first autopsy case of fatal acute cardiac failure after administration of carfilzomib in a patient with multiple myeloma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6512067/
https://www.ncbi.nlm.nih.gov/pubmed/31183224
http://dx.doi.org/10.1155/2019/1816287
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