复发/难治性多发性骨髓瘤临床实践中基于抗cd38治疗的共识指南和建议:来自泛太平洋多发性骨髓瘤工作组

Q4 Health Professions
Clinical hematology international Pub Date : 2025-08-08 eCollection Date: 2025-01-01 DOI:10.46989/001c.141401
Wenming Chen, Zhen Cai, Chor Sang Chim, Wee Joo Chng, Juan Du, Chengcheng Fu, Wen Gao, Ichiro Hanamura, Jian Hou, Jeffrey Shang-Yi Huang, Tadao Ishida, Chunrui Li, Aijun Liu, Vadim Ptushkin, Naoki Takezako, Raymond Siu Ming Wong, Dok Hyun Yoon
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引用次数: 0

摘要

抗cd38单克隆抗体(mab),包括daratumumab和isatuximab,已经成为治疗复发/难治性多发性骨髓瘤(RRMM)的关键成分。这一专家共识为其最佳使用提供了基于证据的指导,包括方案选择、对老年人或体弱患者的特殊考虑以及对高危亚群的治疗。讨论的关键主题包括选择基于抗cd38的方案,根据虚弱和合并症对患者进行分层,管理血液学毒性的策略,以及重新治疗的考虑。基于抗cd38单抗的治疗方案已经在不同的RRMM人群中证明了临床疗效,包括高风险细胞遗传学异常(如1q21+)的患者。虽然耐药仍然是一个临床挑战,特别是在先前暴露的患者中,目前的证据支持在一段相当长的洗脱期(通常为6至12个月)后再挑战抗CD38单抗的可行性,这可能会使CD38表达和免疫效应功能部分恢复。共识还强调了这些药物在老年人或体弱个体中的持续效用,在这些人群中,通过适当的监测和支持性护理可以实现持久的反应。此外,抗cd38单克隆抗体被认为是不断发展的治疗模式中的关键组成部分,支持它们用于包括CAR-T细胞和双特异性抗体等新兴免疫疗法的联合策略。这一共识为指导个体化治疗决策提供了一个框架,并强调了继续研究将抗cd38单克隆抗体优化整合到RRMM现代治疗领域的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Consensus Guidelines and Recommendations for the anti-CD38-based Therapy in Clinical Practice for Relapsed/Refractory Multiple Myeloma: From the Pan-Pacific Multiple Myeloma Working Group.

Anti-CD38 monoclonal antibodies (mAbs), including daratumumab and isatuximab, have become key components of treatment for relapsed/refractory multiple myeloma (RRMM). This expert consensus provides evidence-based guidance on their optimal use, including regimen selection, special considerations for elderly or frail patients, and the treatment of high-risk subgroups. Key topics addressed include the selection of anti-CD38-based regimens, patient stratification by frailty and comorbidities, strategies for managing hematologic toxicities, and considerations for re-treatment. Anti-CD38 mAb-based regimens have demonstrated clinical efficacy across diverse RRMM populations, including patients with high-risk cytogenetic abnormalities such as 1q21+. While resistance remains a clinical challenge, particularly in previously exposed patients, current evidence supports the feasibility of anti-CD38 mAb rechallenge following a substantial washout period (typically 6 to 12 months), which may allow partial recovery of CD38 expression and immune effector function. The consensus also emphasizes the continued utility of these agents in elderly or frail individuals, where durable responses can be achieved with appropriate monitoring and supportive care. Moreover, anti-CD38 mAbs are recognized as key components within evolving treatment paradigms, supporting their use for combination strategies involving emerging immunotherapies such as CAR-T cells and bispecific antibodies. This consensus provides a framework to guide individualized treatment decisions and highlights the need for continued research to optimize the integration of anti-CD38 mAbs into the modern therapeutic landscape of RRMM.

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