替司他抗缓解多发性骨髓瘤患者慢性免疫性血小板减少症

EJHaem Pub Date : 2025-05-25 DOI:10.1002/jha2.70062
Renata Quevedo-Salazar, José Miguel Yáñez-Reyes, Elías Eugenio González-López, Ana Varela-Constantino, Andrés Gómez-De León, Xitlaly Judith González-Leal, David Gómez-Almaguer
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引用次数: 0

摘要

我们报告一例76岁的难治性免疫性血小板减少症(ITP)和多发性骨髓瘤(MM)的妇女,经替司他单抗治疗后,两种情况均得到缓解。多次ITP治疗失败后,她的血小板计数继续下降。开始使用替司他抗可导致血小板快速和持续增加,同时伴有可测量的残余疾病(MRD)阴性的MM反应。值得注意的是,仅在四次全剂量后就实现了缓解,并且此后患者一直处于完全缓解状态。该病例强调了teclistamab作为难治性ITP的潜在治疗方法,提示b细胞成熟抗原(BCMA)靶向治疗在自身免疫性疾病中的新作用。试验注册作者已确认该提交不需要临床试验注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Teclistamab-Induced Remission of Chronic Immune Thrombocytopenia in a Patient With Multiple Myeloma

We report the case of a 76-year-old woman with refractory immune thrombocytopenia (ITP) and multiple myeloma (MM) who achieved remission of both conditions following teclistamab treatment. After failing multiple ITP therapies, her platelet count continued to decline. Initiation of teclistamab led to a rapid and sustained platelet increase, alongside MM response with measurable residual disease (MRD) negativity. Notably, remission was achieved after only four full doses, and the patient has remained in complete remission since. This case highlights teclistamab as a potential treatment for refractory ITP, suggesting a novel role for B-cell maturation antigen (BCMA)-targeted therapies in autoimmune diseases.

Trial Registration

The authors have confirmed clinical trial registration is not needed for this submission.

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