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首页> 外文期刊>Bone marrow transplantation >Benefits of additional cycles of bortezomib/thalidomide/dexamethasone (VTD) induction therapy compared to four cycles of VTD for newly diagnosed multiple myeloma
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Benefits of additional cycles of bortezomib/thalidomide/dexamethasone (VTD) induction therapy compared to four cycles of VTD for newly diagnosed multiple myeloma

机译:与新诊断的多发性骨髓瘤的vtd的四个循环相比,Bortezomib /沙利度胺/地塞米松(VTD)诱导治疗的额外循环(VTD)感应治疗的益处

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摘要

Bortezomib/thalidomide/dexamethasone (VTD) induction therapy followed by autologous stem cell transplantation (ASCT) is one of the standard therapies for newly diagnosed multiple myeloma (NDMM). However, the appropriate depth of response to induction therapy and timing of upfront ASCT are still debated. We investigated if two additional cycles of VTD (VTD6) improved the responses and progression-free survival (PFS) compared with four cycles of VTD (VTD4). We retrospectively reviewed outcomes of 190 NDMM patients treated with at least four cycles of VTD followed by ASCT between September 2014 and August 2017 [VTD4, n = 129 (67.9%); VTD6, n = 61 (32.1%)]. The VTD6 group had a higher pre-ASCT complete response (CR) rate than the VTD4 group (31.1% versus 10.1%, P = very good partial response (VGPR), and 2-year PFS were similar. Multivariate analysis revealed age, beta(2)-microglobulin, and pre-ASCT CR as important factors for PFS. Two additional cycles of VTD prolonged PFS in patients with PR only after VTD4 [Hazard ratio (HR) = 0.29, P = 0.016] or those with Revised International Staging System stage I/II (HR = 0.36, P = 0.039). In conclusion, two additional VTD cycles may be helpful for patients with PR only after VTD4 but high risk MM needs the other treatment options.
机译:Bortezomib /沙利度胺/地塞米松(VTD)感应治疗随后是自体干细胞移植(ASCT)是新诊断的多发性骨髓瘤(NDMM)的标准疗法之一。然而,对对诱导治疗的适当响应和初期asct的时间仍然讨论。我们研究了与VTD(VTD4)的四个循环相比改善了两种VTD(VTD6)的额外循环改善了无响应和无进展生存(PFS)。我们回顾性地审查了190名NDMM患者的结果,治疗了至少四个VTD周期,然后于2014年9月至2017年8月(VTD4,N = 129(67.9%); VTD6,N = 61(32.1%)]。 VTD6组的预先取代完整响应(CR)率高于VTD4组(31.1%对10.1%,P =非常好的部分响应(VGPR)和2年的PFS是相似的。多变量分析显示年龄,β (2)-Microglobulin,以及预先ASCT CR作为PFS的重要因素。PR在VTD4 [危险比(HR)= 0.29,P = 0.016]或经修订的国际分期期间,PR患者的两种额外的VTD延长PFS循环系统阶段I / II(HR = 0.36,P = 0.039)。总之,只有在VTD4之后,PR的患者可能有助于患者,但高风险MM需要其他治疗方案。

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  • 来源
    《Bone marrow transplantation》 |2019年第12期|共9页
  • 作者单位

    Univ Ulsan Coll Med Ulsan Univ Hosp Dept Internal Med Div Hematol &

    Oncol Ulsan South Korea;

    Kyungpook Natl Univ Kyungpook Natl Univ Hosp Sch Med Dept Hematol Oncol Daegu South Korea;

    Kyungpook Natl Univ Kyungpook Natl Univ Hosp Sch Med Dept Hematol Oncol Daegu South Korea;

    Sungkyunkwan Univ Sch Med Samsung Med Ctr Dept Hematol Oncol Seoul South Korea;

    Chonnam Natl Univ Hwasun Hosp Dept Hematol Oncol Hwasun South Korea;

    Chonnam Natl Univ Hwasun Hosp Dept Hematol Oncol Hwasun South Korea;

    Univ Ulsan Coll Med Ulsan Univ Hosp Dept Internal Med Div Hematol &

    Oncol Ulsan South Korea;

    Pusan Natl Univ Hosp Med Res Inst Sch Med Dept Internal Med Div Hematol Oncol Busan South Korea;

    Inje Univ Busan Paik Hosp Dept Hematol Oncol Busan South Korea;

    Dong A Univ Coll Med Dong A Med Ctr Dept Internal Med Busan South Korea;

    Catholic Univ Daegu Sch Med Daegu Catholic Univ Hosp Dept Hematol Oncol Daegu South Korea;

    Yeungnam Univ Med Ctr Dept Hematol Oncol Daegu South Korea;

    Kosin Univ Coll Med Gospel Hosp Dept Internal Med Div Hematol Busan South Korea;

    Sungkyunkwan Univ Sch Med Samsung Med Ctr Dept Hematol Oncol Seoul South Korea;

    Catholic Univ Korea Coll Med Seoul St Marys Hosp Dept Hematol Seoul South Korea;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 治疗学;
  • 关键词

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