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初诊多发性骨髓瘤的治疗方法。

Current approaches to management of newly diagnosed multiple myeloma.

机构信息

Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Multiple Myeloma Service, Department of medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

出版信息

Am J Hematol. 2022 May;97 Suppl 1:S3-S25. doi: 10.1002/ajh.26512. Epub 2022 Mar 10.

Abstract

Major developments in the treatment of multiple myeloma (MM) over the past decade have led to a continued improvement in survival. Significant progress has been made with deeper and longer remissions seen with newer treatment approaches-both for induction as well as maintenance therapy. The treatment approach to MM is guided by several factors including patient age, frailty, comorbidities, eligibility for autologous stem cell transplantation (ASCT), and risk stratification into standard-risk or high-risk MM. High-risk MM is defined by the presence of t(4;14), t(14;16), t(14;20), del (17p), TP53 mutation, or gain (1q). Transplant eligible patients should receive 4-6 cycles of induction followed by stem cell collection. Patients can then undergo ASCT, or continue induction therapy and shift to maintenance, delaying ASCT till first relapse. Transplant ineligible patients should receive induction therapy followed by maintenance. For induction therapy prior to ASCT, a proteasome inhibitor-IMiD combination remains standard with monoclonal antibody-based quadruplets preferred in high-risk patients. Among transplant ineligible patients, those with standard-risk MM should receive DRd continued until disease progression, while bortezomib containing regimens (VRd or VRd lite) can be considered for high-risk patients. Finally, standard-risk patients should receive lenalidomide maintenance after induction/ASCT, while proteasome inhibitor-IMiD combinations should be used for high-risk patients.

摘要

过去十年中,多发性骨髓瘤(MM)的治疗取得了重大进展,患者的生存率持续提高。随着新的治疗方法的应用,患者获得了更深层次和更持久的缓解,无论是诱导缓解还是维持治疗。MM 的治疗方法受到多种因素的影响,包括患者年龄、虚弱程度、合并症、自体干细胞移植(ASCT)的资格以及标准风险或高风险 MM 的风险分层。高风险 MM 的定义是存在 t(4;14)、t(14;16)、t(14;20)、del(17p)、TP53 突变或 1q 增益。有资格进行移植的患者应接受 4-6 个周期的诱导治疗,然后进行干细胞采集。然后,患者可以接受 ASCT,或者继续进行诱导治疗并转为维持治疗,延迟 ASCT 直到首次复发。不适合进行移植的患者应接受诱导治疗和维持治疗。对于 ASCT 前的诱导治疗,蛋白酶体抑制剂-免疫调节剂(IMiD)联合仍然是标准治疗方案,而在高危患者中,基于单克隆抗体的四联方案更受欢迎。对于不适合移植的患者,标准风险 MM 患者应继续接受 DRd 治疗,直至疾病进展,而含硼替佐米的方案(VRd 或 VRd lite)可用于高危患者。最后,标准风险患者应在诱导/ASCT 后接受来那度胺维持治疗,而高危患者应使用蛋白酶体抑制剂-IMiD 联合治疗。

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