Chen Wenming, Cai Zhen, Chim Chor Sang, Chng Wee Joo, Du Juan, Fu Chengcheng, Gao Wen, Hanamura Ichiro, Hou Jian, Huang Jeffrey Shang-Yi, Ishida Tadao, Li Chunrui, Liu Aijun, Ptushkin Vadim, Takezako Naoki, Wong Raymond Siu Ming, Yoon Dok Hyun
Department of Hematology, Myeloma Research Center of Beijing, Beijing Chaoyang Hospital, Capital Medical University, Beijingk, China.
Bone Marrow Transplantation Center, the First Affiliated Hospital, Zhejiang University School of Medicine, Zhejiang, China.
Clin Hematol Int. 2025 Aug 8;7(3):36-59. doi: 10.46989/001c.141401. eCollection 2025.
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.
抗CD38单克隆抗体(mAb),包括达雷妥尤单抗和isatuximab,已成为复发/难治性多发性骨髓瘤(RRMM)治疗的关键组成部分。本专家共识为其最佳使用提供了循证指导,包括方案选择、老年或体弱患者的特殊考虑以及高危亚组的治疗。涉及的关键主题包括基于抗CD38方案的选择、根据虚弱程度和合并症对患者进行分层、血液学毒性管理策略以及再治疗的考虑因素。基于抗CD38 mAb的方案在不同的RRMM人群中已显示出临床疗效,包括具有高危细胞遗传学异常(如1q21+)的患者。虽然耐药性仍然是一个临床挑战,尤其是在既往接受过治疗的患者中,但目前的证据支持在经过较长洗脱期(通常为6至12个月)后再次使用抗CD38 mAb的可行性,这可能使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或体弱个体中的持续效用,通过适当的监测和支持性护理可以实现持久缓解。此外,抗CD38 mAb被认为是不断发展的治疗模式中的关键组成部分,支持将其用于涉及新兴免疫疗法(如CAR-T细胞和双特异性抗体)的联合策略。本共识提供了一个指导个体化治疗决策的框架,并强调了持续研究以优化抗CD38 mAb融入RRMM现代治疗格局的必要性。