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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

机译:年轻的多发性骨髓瘤患者单独使用新药诱导疗法或自体干细胞移植后疗法:114例单中心回顾性研究

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摘要

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 de novo 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.
机译:为了确定新药时代下自体干细胞移植(ASCT)在新诊断的多发性骨髓瘤(MM)中的作用,我们分析了单独或单独使用这些药物治疗的患者的随访数据。从2008年1月到2012年12月,有136名年龄小于65岁的MM新患者完成了以硼替佐米或沙利度胺为基础的诱导治疗,其中114例至少达到了部分缓解(PR)。共有42例患者接受了ASCT。中位随访39个月(5-74个月)后,非ASCT组中位无进展生存期(PFS)为23个月,而ASCT组为42个月(P = 0.001),和5年总生存率分别为58.9和81.2%(P = 0.03)。多元分析显示,两组的完全缓解(CR)和维持治疗(MT)是改善OS的独立因素。此外,根据反应状态进行了亚组分析,以评估ASCT和MT的作用。在CR亚组中,ASCT和MT均未对PFS或OS产生显着影响。在非常好的PR子组中,MT后ASCT(ASCT / MT)可以显着改善PFS,但不能改善OS。在表现出PR的患者中,ASCT / MT可显着延长PFS和OS。因此,在新药时代,ASCT在年轻的MM患者中,尤其是在诱导治疗后达到PR的患者中,起着重要的作用。此外,MT是与所有MM患者长期生存相关的关键因素。

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