首页> 外文期刊>Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation >Allogeneic Stem Cell Transplantation in Therapy-Related Myelodysplasia after Autologous Transplantation for Lymphoma: A Retrospective Study of the Francophone Society of Bone Marrow Transplantation and Cellular Therapy
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Allogeneic Stem Cell Transplantation in Therapy-Related Myelodysplasia after Autologous Transplantation for Lymphoma: A Retrospective Study of the Francophone Society of Bone Marrow Transplantation and Cellular Therapy

机译:淋巴瘤自体移植后治疗相关髓细胞癌的同种异体干细胞移植:骨髓移植和细胞疗法的特写社会回顾性研究

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Therapy-related myelodysplastic syndrome (t-MDS) after autologous stem cell transplantation (ASCT) is a rare complication with no curative option. Allogeneic hematopoietic stem cell transplantation (allo-HSCT) may be considered for eligible patients and has been understudied in t-MDS. We report 47 consecutive patients with t-MDS after an ASCT who underwent allo-HSCT with a median age of 58 years (range, 30 to 71 years) at transplantation and a median follow-up of 22 months (range, 0.7 to 107). The median overall survival (OS) was 6.9 months (95% confidence interval [CI], 0 to 19 months). OS rates were 45% (29% to 60%) and 30% (15% to 45%) at 1 and 3 years after transplantation, respectively. On univariate analysis, prior therapy for t-MDS before allo-HSCT (P = .02) and mismatched donors (P = .004) were associated with poor OS. Three-year nonrelapse mortality (NRM) and relapse rates were 44% (25% to 63%) and 41% (22% to 61%), respectively. Mismatched donors (P < .001) were associated with higher NRM and a high-risk MDS (P = .008) with a higher relapse risk. On multivariate analysis, HLA mismatch was associated with higher NRM (hazard ratio, 6.21; 95% CI, 1.63 to 23.62; P = .007). In conclusion, our results suggest that one third of the patients who develop t-MDS after an ASCT for lymphoma are cured after an allo-HSCT. The use of mismatched donors with standard graft-versus-host disease prophylaxis should be avoided in such an indication for allo-HSCT. It will be worthwhile to see if the implementation of cyclophosphamide post-transplantation will improve the outcome with mismatched donors. (C) 2019 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc.
机译:自体干细胞移植(ASCT)后治疗相关的髓细胞增生综合征(T-MDS)是罕见的并非治疗选择。组分造血干细胞移植(Allo-HSCT)可考虑符合条件的患者,并在T-MDS中被解读。在ASCT后,在ASCT后,在移植的58岁(范围为30至71岁)的allo-hsct后,连续47名连续患有T-MDS的患者,中位数为22个月(范围,0.7至107) 。中位数总存活(OS)为6.9个月(95%置信区间[CI],0至19个月)。在移植后1和3年,OS率分别为45%(29%至60%)和30%(15%至45%)。在单变量分析中,在Allo-HSCT(P = 0.02)和不匹配的供体(P = .004)之前对T-MDS的先前治疗与差的OS相关。三年的非筛选死亡率(NRM)和复发率分别为44%(25%至63%),分别为41%(22%至61%)。不匹配的供体(P <.001)与较高的NRM和高风险MDS(P = .008)相关,复发风险较高。在多变量分析中,HLA失配与较高的NRM(危险比,6.21; 95%CI,1.63至23.62; P = .007)。总之,我们的结果表明,在ALCT-HSCT后,在ASCT后开发T-MDS的患者中的三分之一。在此类指示中,应避免使用标准移植物与宿主疾病预防的错配供体。值得看看移植后环磷酰胺的实施是否会改善不匹配的供体的结果。 (c)2019年美国移植和细胞疗法。 elsevier公司发布

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