首页> 外文期刊>Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation >Post-Transplant Outcomes in High-Risk Compared with Non-High-Risk Multiple Myeloma: A CIBMTR Analysis
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Post-Transplant Outcomes in High-Risk Compared with Non-High-Risk Multiple Myeloma: A CIBMTR Analysis

机译:与非高风险多发性骨髓瘤相比,高风险的移植后结果:CIBMTR分析

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Conventional cytogenetics and interphase fluorescence in situ hybridization (FISH) identify high-risk multiple myeloma (HRM) populations characterized by poor outcomes. We analyzed these differences among HRM versus non-HRM populations after upfront autologous hematopoietic cell transplantation (autoHCT). Between 2008 and 2012, 715 patients with multiple myeloma identified by 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 HRM patients (17.5%), induction with bortezomib and immunomodulatory agents (imids) was higher compared with non-HRM (56% versus 43%, P <.001) with similar pretransplant complete response (CR) rates (14% versus 16%, P.1). At day 100 post-transplant, at least a very good partial response was 59% in HRM and 61% in non-HRM (P =.6). More HRM patients received post transplant therapy with bortezomib and imids (26% versus 12%, P =.004). Three-year post-transplant progression free (PFS) and overall survival (OS) rates in HRM versus non-HRM were 37% versus 49% (P <.001) and 72% versus 85% (P <.001), respectively. At 3 years, PFS for HRM patients with and without post-transplant therapy was 46% (95% confidence interval [CI], 33 to 59) versus 14% (95% CI, 4 to 29) and in non-HRM patients with and without post-transplant therapy 55% (95% CI, 49 to 62) versus 39% (95%.CI, 32 to 47); rates of OS for HRM patients with and without post-transplant therapy were 81% (95% CI, 70 to 90) versus 48% (95% CI, 30 to 65) compared with 88% (95% CI, 84 to 92) and 79% (95% CI, 73 to 85) in non-HRM patients 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 =.08). In addition to HRM, higher stage, less than a CR pretransplant, 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 with non-HRM patients, but these resporises are not sustained. Post-transplant therapy appeared to improve the poor outcomes of HRM. (C) 2016 American Society for Blood and Marrow Transplantation.
机译:常规的细胞遗传学和相间荧光原位杂交(FISH)可以鉴定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人群之间的这些差异。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,通过FISH和/或具有前期autoHCT的细胞遗传学数据鉴定的715例多发性骨髓瘤患者。 HRM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;所有其他人都是非人力资源经理。在125例HRM患者中(17.5%),与非HRM相比,硼替佐米和免疫调节剂(imids)的诱导率更高(56%对43%,P <.001),而移植前完全缓解(CR)率相近(14%对16%,第1页)。移植后第100天,HRM至少有很好的局部缓解,非HRM至少有61%(P = .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 = .004)。 HRM与非HRM的三年移植后无进展(PFS)和总生存(OS)率分别为37%对49%(P <.001)和72%对85%(P <.001) 。在3年时,接受和不接受移植后治疗的HRM患者的PFS为46%(95%置信区间[CI]为33至59),而非HRM患者为14%(95%CI为4至29)。且未进行移植后治疗的比例为55%(95%CI,49-62),而39%(95%CI,32-47);接受和不接受移植后治疗的HRM患者的OS率分别为81%(95%CI,70至90)和48%(95%CI,30至65),而88%(95%CI,84至92)接受和不接受移植后治疗的非HRM患者分别为79%(95%CI,73至85)。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 = .08)。除HRM外,更高的阶段,少于CR的移植前,缺乏移植后治疗以及非裔美国人种族与较差的OS有关。总之,我们显示,与非HRM患者相比,HRM患者在移植后第100天获得了相似的反应,但是这些表现没有持续。移植后治疗似乎可以改善HRM的不良预后。 (C)2016美国血液和骨髓移植学会。

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