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复发性难治性多发性骨髓瘤患者经 idecabtagene vicleucel 成功控制心脏淀粉样变性:一例病例报告及文献综述

英文原题:A successful control of cardiac amyloidosis by idecabtagene vicleucel in a patient with relapsed and refractory multiple myeloma: a case report and literature review.

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A successful control of cardiac amyloidosis by idecabtagene vicleucel in a patient with relapsed and refractory multiple myeloma: a case report and literature review.

PubMed 2025/06/14(内容时间) Int J Hematol Q3 · IF 1.9(JCR 2025)

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中文摘要

一名50岁日本男性,患五药难治性多发性骨髓瘤(MM),在接受idecabtagene vicleucel(ide-cel)治疗前被发现患有IIIa期心脏免疫球蛋白轻链淀粉样变性。经过慎重考虑并经医院伦理委员会批准后,开始ide-cel治疗。ide-cel输注后急性期出现3级细胞因子释放综合征和心房扑动,但在重症监护室通过支持治疗均耐受良好。患者在ide-cel输注后第60天达到严格完全缓解,第9个月达到心脏缓解,并于第133天因持续性心房扑动接受了导管消融。自ide-cel治疗以来,他已维持血液学和心脏缓解超过1年。本病例凸显了ide-cel在重度经治MM合并心脏淀粉样变性中控制疾病的有效性。

展开英文摘要原文

A 50-year-old Japanese man with penta-drug refractory multiple myeloma (MM) was found to have stage IIIa cardiac immunoglobulin light-chain amyloidosis before idecabtagene vicleucel (ide-cel) therapy. Ide-cel therapy was started after careful consideration and hospital ethics committee approval. Grade 3 cytokine release syndrome and atrial flutter occurred in the acute phase after ide-cel infusion, but these were well-tolerated with supportive care in the intensive care unit.

The patient achieved stringent complete response at day 60 and cardiac response at 9 months after ide-cel infusion with the addition of catheter ablation for sustained atrial flutter on day 133. He has maintained both hematological and cardiac remission for over 1 year since ide-cel therapy. This case highlights the effectiveness of ide-cel for disease control in heavily pretreated MM with cardiac amyloidosis.

论文信息

作者
Ueda Y、Terao T、Fujii N、Mino T、Kubota S、Hayashino K、Fujiwara K、Kondo T
第一作者单位
Department of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.Japan
通讯作者单位
Department of Hematology and Oncology, Okayama University Hospital, Okayama, Japan. nfujii@md.okayama-u.ac.jp.Japan
文献类型
病例报告 · 综述
期刊
International journal of hematology2025 Oct
原文标识
PubMed 40514575 · DOI 10.1007/s12185-025-04016-x