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新型药物诱导疗法单独应用或在年轻多发性骨髓瘤患者中序贯自体干细胞移植:一项114例患者的单中心回顾性研究

Novel agent induction therapy alone or followed by autologous stem cell transplantation in younger patients with multiple myeloma: A single-center retrospective study of 114 cases.

作者信息

Wang Yan, Xu Pengpeng, Chen Yubao, Fan Qingye, Li Junmin, Zhao Weili, Mi Jianqing, Yan Hua

机构信息

Department of Hematology, Ruijin Hospital, Shanghai Jiao-Tong University School of Medicine, Shanghai 200025, P.R. China.

出版信息

Mol Clin Oncol. 2016 Jan;4(1):107-113. doi: 10.3892/mco.2015.658. Epub 2015 Oct 16.

Abstract

To define the role of autologous stem cell transplantation (ASCT) in newly diagnosed multiple myeloma (MM) in the era of novel agents, we analyzed follow-up data of patients treated by these agents alone or followed by ASCT. From January, 2008 to December, 2012, 136 patients with MM, aged <65 years, completed bortezomib- or thalidomide-based induction therapy and 114 patients achieved at least a partial response (PR). A total of 42 patients underwent ASCT. After a median follow-up of 39 months (range, 5-74 months), the median progression-free survival (PFS) was 23 months in the non-ASCT group vs. 42 months in the ASCT group (P=0.001), and the 5-year overall survival (OS) rate was 58.9 vs. 81.2%, respectively (P=0.03). The multivariate analysis revealed that complete response (CR) and maintenance therapy (MT) were independent factors of improved OS in both groups. Moreover, a subgroup analysis was performed according to the response status to evaluate the role of ASCT and MT. In the CR subgroup, neither ASCT nor MT exerted a significant effect on PFS or OS. In the very good PR subgroup, ASCT after MT (ASCT/MT) significantly improved PFS, but not OS. In patients exhibiting PR, ASCT/MT significantly prolonged PFS and OS. Therefore, ASCT in the era of novel agents maintains an important role in younger MM patients, particularly those achieving a PR after induction therapy. Furthermore, MT is a key factor associated with long-term survival in all MM patients.

摘要

为了明确在新型药物时代自体干细胞移植(ASCT)在新诊断的多发性骨髓瘤(MM)中的作用,我们分析了单独接受这些药物治疗或随后接受ASCT治疗的患者的随访数据。2008年1月至2012年12月,136例年龄<65岁的MM患者完成了基于硼替佐米或沙利度胺的诱导治疗,114例患者至少达到部分缓解(PR)。共有42例患者接受了ASCT。中位随访39个月(范围5 - 74个月)后,非ASCT组的中位无进展生存期(PFS)为23个月,而ASCT组为42个月(P = 0.001),5年总生存率(OS)分别为58.9%和81.2%(P = 0.03)。多因素分析显示,完全缓解(CR)和维持治疗(MT)是两组中OS改善的独立因素。此外,根据缓解状态进行亚组分析以评估ASCT和MT的作用。在CR亚组中,ASCT和MT对PFS或OS均未产生显著影响。在非常好的PR亚组中,MT后ASCT(ASCT/MT)显著改善了PFS,但未改善OS。在表现为PR的患者中,ASCT/MT显著延长了PFS和OS。因此,在新型药物时代,ASCT在年轻MM患者中仍发挥着重要作用,尤其是那些诱导治疗后达到PR的患者。此外,MT是所有MM患者长期生存的关键因素。

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Am Soc Clin Oncol Educ Book. 2012:515-22. doi: 10.14694/EdBook_AM.2012.32.21.

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