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Post-transplant outcomes in high-risk compared to non-high risk multiple myeloma a CIBMTR analysis

机译:CIBMTR分析与非高风险多发性骨髓瘤相比高风险的移植后预后

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摘要

Conventional cytogenetics and interphase fluorescence in-situ hybridization (FISH) identify a high-risk multiple myeloma (HRM) population characterized by poor outcomes. We analyzed these differences among HRM versus non-HRM after upfront autologous hematopoietic cell transplantation (autoHCT). Between 2008 and 2012, 715 patients with multiple myeloma with FISH and/or cytogenetic data with upfront autoHCT were identified in the Center for International Blood and Marrow Transplant Research database. HRM was defined as del17p, t(4;14), t(14;16), hypodiploidy (< 45 chromosomes excluding -Y) or chromosome 1 p and 1q abnormalities; all others were non-HRM. Among 125 (17.5%) HRM patients, induction with bortezomib and immunomodulatory agents (imid) was higher compared to non-HRM (56% vs 43%, p <0.001) with similar pre-transplant complete response (CR) (14% vs 16%, p 0.1). At day-100 post-transplant, ≥ very good partial response was 59% in HRM and 61% in non-HRM (p=0.6). More HRM patients received post-transplant therapy with bortezomib and imids (26% vs 12%, p=0.004). Three-year post-transplant progression-free (PFS) and overall survival (OS) in HRM versus non-HRM were 37% vs 49%, p <0.001 and 72% vs 85%, p <0.001 respectively. At 3-years, PFS for HRM with and without post-transplant therapy was 46(95% confidence interval 33–59)% versus 14(4–29)% and in non-HRM with and without post-transplant therapy 55(49–62)% versus 39(32–47)%; OS for HRM with and without post-transplant therapy was 81(70–90)% versus 48(30–65)% compared to 88(84–92)% and 79(73–85)% in non-HRM with and without post-transplant therapy respectively. Among patients receiving post-transplant therapy, there was no difference in OS between HRM and non-HRM (p 0.08). In addition to HRM, higher stage, <CR pre-transplant, lack of post-transplant therapy and African-American race were associated with worse OS. In conclusion, we show HRM patients achieve similar day-100 post-transplant responses compared to non-HRM, but these responses are not sustained. Post-transplant therapy appeared to improve the poor outcomes of HRM.
机译:常规的细胞遗传学和相间荧光原位杂交(FISH)可以识别出以不良预后为特征的高危多发性骨髓瘤(HRM)人群。我们分析了前期自体造血细胞移植(autoHCT)后HRM与非HRM之间的这些差异。在2008年至2012年之间,在国际血液和骨髓移植研究中心数据库中识别出715例具有FISH和/或细胞遗传学数据且具有前期autoHCT的多发性骨髓瘤患者。 HRM被定义为del17p,t(4; 14),t(14; 16),二倍体性(<45个染色体,不包括-Y)或1p和1q染色体异常;所有其他都是非人力资源管理。在125名(17.5%)HRM患者中,与相似的移植前完全缓解(CR)的非HRM(56%vs 43%,p <0.001)相比,硼替佐米和免疫调节剂(imid)的诱导率更高(14%vs. 16%,P = 0.1)。移植后第100天,≥很好的部分反应在HRM中为59%,在非HRM中为61%(p = 0.6)。更多的HRM患者接受了硼替佐米和亚胺类药物的移植后治疗(26%比12%,p = 0.004)。与非HRM相比,HRM的三年移植后无进展(PFS)和总生存期(OS)分别为37%vs 49%,p <0.001和72%vs 85%,p <0.001。在3年时,有或没有移植后治疗的HRM患者的PFS为46(95%置信区间33–59)%,而有和没有移植后治疗的非HRM患者的PFS为14(4–29)%55(49) –62)%和39(32–47)%;有和没有移植后治疗的HRM的OS分别为81(70-90)%和48(30-65)%,相比之下,有无HRM的有无HRM的OS为88(84-92)%和79(73-85)%移植后治疗。在接受移植后治疗的患者中,HRM和非HRM之间的OS没有差异(p = 0.08)。除HRM外,更高的阶段,

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