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多发性骨髓瘤异基因造血干细胞移植的历史回顾

Historical Perspective of Allogeneic Hematopoietic Stem Cell Transplantation for Multiple Myeloma.

作者信息

Aslam Muhammad Faisal, Cheema Asfand Yar, Shahid Daniyal, Maryam Bibi, Mukhopadhyay Debduti, Munir Mishaal, Najam Ali, Ali Hossam M, Bashir Qaiser, Anwer Faiz

机构信息

Department of Medicine, Ascension St. Vincent's East Hospital, Birmingham, Alabama, USA.

Department of Medicine/Taussig Cancer Center, Cleveland Clinic, Cleveland, Ohio, USA.

出版信息

Acta Haematol. 2025;148(3):315-329. doi: 10.1159/000542704. Epub 2024 Nov 25.

Abstract

BACKGROUND

Advances in novel therapies have improved outcomes for multiple myeloma (MM) patients and the use of allo-SCT has decreased. Current guidelines no longer support allo-SCT as consolidation therapy for newly diagnosed MM, even in high-risk cases.

SUMMARY

Allo-SCT is now typically considered only within clinical trials for young, high-risk patients with relapsed or refractory MM (RRMM). It has not proven favorable despite its historical use. CAR T-cell therapy and bispecific antibodies have shown promise in treating triple- and penta-exposed/refractory MM, yet relapse remains common with poor survival rates. The efficacy of allo-SCT following BCMA-directed therapy and other new T-cell-directed therapies is unclear. Allo-SCT might be a viable option for eligible patients who relapse after these therapies, or where such options are unavailable. Advancements in reduced-intensity conditioning regimens have led to lower toxicity and transplant-related (TR) morbidity, lower graft-versus-host disease (GvHD), and TR mortality. Expanded use of alternative donors, like haploidentical donors, has yielded comparable outcomes. Better post-transplant GvHD regimens and maintenance strategies to prevent relapse have been developed.

KEY MESSAGES

This review analyzes available literature to better understand the safety, efficacy, and current role of allo-SCT in managing MM. Newer regimens are needed as routine use of allo-SCT cannot be recommended.

摘要

背景

新型疗法的进展改善了多发性骨髓瘤(MM)患者的治疗效果,异基因造血干细胞移植(allo-SCT)的使用减少。当前指南不再支持将allo-SCT作为新诊断MM的巩固治疗方法,即使在高危病例中也是如此。

总结

目前,allo-SCT通常仅在针对复发或难治性MM(RRMM)的年轻高危患者的临床试验中考虑使用。尽管其有过历史应用,但尚未证明其具有优势。嵌合抗原受体(CAR)T细胞疗法和双特异性抗体在治疗三重和五重暴露/难治性MM方面显示出前景,但复发仍然常见,生存率较低。在靶向B细胞成熟抗原(BCMA)的疗法和其他新的靶向T细胞的疗法之后进行allo-SCT的疗效尚不清楚。对于在这些疗法后复发的符合条件的患者,或者在没有此类选择的情况下,allo-SCT可能是一个可行的选择。降低强度预处理方案的进展导致毒性和移植相关(TR)发病率降低,移植物抗宿主病(GvHD)和TR死亡率降低。扩大使用替代供体,如单倍体相合供体,已产生了可比的结果。已经开发出更好的移植后GvHD方案和预防复发的维持策略。

关键信息

本综述分析了现有文献,以更好地了解allo-SCT在治疗MM中的安全性、疗效和当前作用。由于不建议常规使用allo-SCT,因此需要更新的方案。

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本文引用的文献

4
New Biological Therapies for Multiple Myeloma.多发性骨髓瘤的新型生物疗法。
Annu Rev Med. 2024 Jan 29;75:13-29. doi: 10.1146/annurev-med-050522-033815. Epub 2023 Sep 30.

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