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异基因造血干细胞移植治疗多发性骨髓瘤的长期疗效。

Long-term outcome after allogeneic stem cell transplantation in multiple myeloma.

机构信息

Comprehensive Cancer Center, Department of Hematology, Helsinki University Hospital and University of Helsinki, Haartmaninkatu 4, P.O. Box 372, 00290, Helsinki, Finland.

Department of Medicine, Kuopio University Hospital, Kuopio, Finland.

出版信息

Ann Hematol. 2021 Jun;100(6):1553-1567. doi: 10.1007/s00277-021-04514-y. Epub 2021 Apr 17.

DOI:10.1007/s00277-021-04514-y
PMID:33866396
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8116307/
Abstract

The role of allogeneic hematopoietic stem cell transplantation (allo-SCT) in multiple myeloma is controversial. We analyzed the results of 205 patients transplanted in one center during 2000-2017. Transplantation was performed on 75 patients without a previous autologous SCT (upfront-allo), on 74 as tandem transplant (auto-allo), and on 56 patients after relapse. Median overall survival (OS) was 9.9 years for upfront-allo, 11.2 years for auto-allo, and 3.9 years for the relapse group (p = 0.015). Progression-free survival (PFS) was 2.4, 2.4, and 0.9 years, respectively (p < 0.001). Non-relapse mortality at 5 years was 8% overall, with no significant difference between the groups. Post-relapse survival was 4.1 years for upfront-allo and auto-allo, and 2.6 years for the relapse group (p = 0.066). Survival of high-risk patients was reduced. In multivariate analysis, the auto-allo group had improved OS and chronic graft-versus-host disease was advantageous in terms of PFS, OS, and relapse incidence. Late relapses occurred in all groups. Allo-SCT resulted in long-term survival in a small subgroup of patients. Our results indicate that auto-allo-SCT is feasible and could be considered for younger patients in the upfront setting.

摘要

异基因造血干细胞移植(allo-SCT)在多发性骨髓瘤中的作用存在争议。我们分析了 2000-2017 年期间在一个中心接受移植的 205 例患者的结果。75 例患者未接受先前的自体 SCT( upfront-allo),74 例患者接受了串联移植(auto-allo),56 例患者在复发后接受了移植。 upfront-allo、auto-allo 和复发组的中位总生存期(OS)分别为 9.9 年、11.2 年和 3.9 年(p = 0.015)。无进展生存期(PFS)分别为 2.4、2.4 和 0.9 年(p < 0.001)。5 年时非复发死亡率总体为 8%,各组间无显著差异。 upfront-allo 和 auto-allo 的复发后生存率为 4.1 年,复发组为 2.6 年(p = 0.066)。高危患者的生存情况有所下降。多变量分析显示,auto-allo 组 OS 改善,慢性移植物抗宿主病有利于 PFS、OS 和复发发生率。所有组均发生晚期复发。allo-SCT 使一小部分患者获得了长期生存。我们的结果表明,自体 allo-SCT 是可行的,并且可以考虑用于初诊时年轻患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/810d/8116307/f304d14e2eb9/277_2021_4514_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/810d/8116307/d1c48691f971/277_2021_4514_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/810d/8116307/f304d14e2eb9/277_2021_4514_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/810d/8116307/d1c48691f971/277_2021_4514_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/810d/8116307/f304d14e2eb9/277_2021_4514_Fig2_HTML.jpg

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