TY - JOUR
T1 - Case Report
T2 - Cardiac Tamponade in Association With Cytokine Release Syndrome Following CAR-T Cell Therapy
AU - Moriyama, Shohei
AU - Fukata, Mitsuhiro
AU - Yokoyama, Taku
AU - Ueno, Shohei
AU - Nunomura, Takuya
AU - Mori, Yasuo
AU - Kato, Koji
AU - Miyamoto, Toshihiro
AU - Akashi, Koichi
N1 - Funding Information:
This work was supported by JSPS KAKENHI Grant Number JP17K11577.
Funding Information:
KK received research funding from Chugai Pharmaceutical, Takeda Pharmaceutical, Kyowa Kirin, AbbVie, Novartis, Eisai, Janssen, Celgene, Ono Pharmaceutical, Daiichi Sankyo, and honorarium from Chugai Pharmaceutical, Takeda Pharmaceutical, Kyowa Kirin, Novartis. KA received research funding from Chugai Pharmaceutical, Takeda Pharmaceutical, Kyowa Kirin, AbbVie, Eisai, Ono Pharmaceutical, Asahi Kasei, Shionogi, Sumitomo Dainippon Pharma, Otsuka Pharmaceutical, Taiho Pharmaceutical, Astellas Pharma, and honorarium from AbbVie, Eisai. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher Copyright:
Copyright © 2022 Moriyama, Fukata, Yokoyama, Ueno, Nunomura, Mori, Kato, Miyamoto and Akashi.
PY - 2022/3/21
Y1 - 2022/3/21
N2 - Chimeric antigen receptor T (CAR-T) cell therapy has been shown to have substantial efficacy against refractory hematopoietic malignancies. However, it frequently causes cytokine release syndrome (CRS) as a treatment-specific adverse event. Although cardiovascular events associated with CAR-T cell therapy have been increasingly reported recently, pericardial disease is a rare complication and its clinical course is not well characterized. Here, we report a case of acute pericardial effusion with cardiac tamponade after CAR-T cell therapy. Case Summary: A 59-year-old man with refractory diffuse large B-cell lymphoma underwent CAR-T cell therapy. Grade 2 CRS was observed on day 0; it progressed to grade 4 on day 7 and was accompanied by a fever over 39°C, hypoxia requiring intubation, hypotension requiring the use of a vasopressor agent, and supraventricular tachycardia. Although cardiac function was preserved, marked pericardial effusion with the collapse of the right heart was detected on echocardiography. Since pericardiocentesis was considered to have a high complication risk due to severe myelosuppression, medications for CRS were prioritized. Tocilizumab, an interleukin-6 inhibitor, and high-dose methylprednisolone (1 g/day for 3 days) were administered for the management of severe CRS. On day 8, the pericardial effusion decreased, and the hemodynamic status markedly stabilized. CRS did not exacerbate after the steroid dose was reduced. Further, lymphoma size reduced after the induction of CAR-T cell therapy, and tumor regrowth was not noted at 3 months after CAR-T cell infusion. Conclusion: Interleukin-6 pathway inhibitors and corticosteroid therapy should be considered in the context of CRS for significant pericardial effusion after CAR-T cell therapy in the acute phase.
AB - Chimeric antigen receptor T (CAR-T) cell therapy has been shown to have substantial efficacy against refractory hematopoietic malignancies. However, it frequently causes cytokine release syndrome (CRS) as a treatment-specific adverse event. Although cardiovascular events associated with CAR-T cell therapy have been increasingly reported recently, pericardial disease is a rare complication and its clinical course is not well characterized. Here, we report a case of acute pericardial effusion with cardiac tamponade after CAR-T cell therapy. Case Summary: A 59-year-old man with refractory diffuse large B-cell lymphoma underwent CAR-T cell therapy. Grade 2 CRS was observed on day 0; it progressed to grade 4 on day 7 and was accompanied by a fever over 39°C, hypoxia requiring intubation, hypotension requiring the use of a vasopressor agent, and supraventricular tachycardia. Although cardiac function was preserved, marked pericardial effusion with the collapse of the right heart was detected on echocardiography. Since pericardiocentesis was considered to have a high complication risk due to severe myelosuppression, medications for CRS were prioritized. Tocilizumab, an interleukin-6 inhibitor, and high-dose methylprednisolone (1 g/day for 3 days) were administered for the management of severe CRS. On day 8, the pericardial effusion decreased, and the hemodynamic status markedly stabilized. CRS did not exacerbate after the steroid dose was reduced. Further, lymphoma size reduced after the induction of CAR-T cell therapy, and tumor regrowth was not noted at 3 months after CAR-T cell infusion. Conclusion: Interleukin-6 pathway inhibitors and corticosteroid therapy should be considered in the context of CRS for significant pericardial effusion after CAR-T cell therapy in the acute phase.
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UR - http://www.scopus.com/inward/citedby.url?scp=85138578391&partnerID=8YFLogxK
U2 - 10.3389/fcvm.2022.848091
DO - 10.3389/fcvm.2022.848091
M3 - Article
AN - SCOPUS:85138578391
SN - 2297-055X
VL - 9
JO - Frontiers in Cardiovascular Medicine
JF - Frontiers in Cardiovascular Medicine
M1 - 848091
ER -