[Outcomes of 138 myelodysplastic syndrome patients with HLA-matched sibling donor allogeneic hematopoietic stem cell transplantation]

Zhonghua Xue Ye Xue Za Zhi. 2020 Feb 14;41(2):132-137. doi: 10.3760/cma.j.issn.0253-2727.2020.02.009.
[Article in Chinese]

Abstract

Objective: To evaluate the outcomes of myelodysplastic syndromes (MDS) patients who received HLA-matched sibling donor allogeneic peripheral blood stem cell transplantation (MSD-PBSCT) . Methods: The clinical data of 138 MDS patients received MSD-PBSCT from Sep. 2005 to Dec. 2017 were retrospectively analyzed, and the overall survival (OS) rate, disease-free survival (DFS) rate, relapse rate (RR) , non-relapse mortality (NRM) rate and the related risk factors were explored. Results: ①After a median follow-up of 1 050 (range 4 to 4 988) days, the 3-year OS and DFS rates were (66.6±4.1) % and (63.3±4.1) %, respectively. The 3-year cumulative incidence of RR and NRM rates were (13.9±0.1) % and (22.2±0.1) %, respectively. ②Univariate analysis showed that patients with grade Ⅲ-Ⅳ acute graft-versus-host disease (aGVHD) or hematopoietic cell transplantation comorbidity index (HCT-CI) ≥2 points or patients in very high-risk group of the Revised International Prognostic Scoring System (IPSS-R) had significantly decreased OS[ (42.9±13.2) %vs (72.9±4.2) %, χ(2)=8.620, P=0.003; (53.3±7.6) %vs (72.6±4.7) %, χ(2)=6.681, P=0.010; (53.8±6.8) %vs (76.6±6.2) %vs (73.3±7.7) %, χ(2)=6.337, P=0.042]. For MDS patients with excess blasts-2 (MDS-EB2) and acute myeloid leukemia patients derived from MDS (MDS-AML) , pre-transplant chemotherapy or hypomethylating agents (HMA) therapy could not improve the OS rate[ (60.4±7.8) %vs (59.2±9.6) %, χ(2)=0.042, P=0.838]. ③Multivariate analysis indicated that the HCT-CI was an independent risk factor for OS and DFS (P=0.012, HR=2.108, 95%CI 1.174-3.785; P=0.008, HR=2.128, 95%CI 1.219-3.712) . Conclusions: HCT-CI was better than the IPSS-R in predicting the outcomes after transplantation. The occurrence of grade Ⅲ-Ⅳ aGVHD is a poor prognostic factor for OS. For patients of MDS-EB2 and MDS-AML, immediate transplantation was recommended instead of receiving pre-transplant chemotherapy or HMA therapy.

目的: 评价人组织相容性抗原(HLA)匹配同胞供者外周血干细胞移植(MSD-PBSCT)治疗骨髓增生异常综合征(MDS)的疗效。 方法: 回顾性总结2005年9月至2017年12月接受MSD-PBSCT治疗的138例MDS患者临床资料,观察患者总生存(OS)率、无病生存(DFS)率、复发(RR)率及非复发死亡率(NRM),分析影响移植预后的危险因素。 结果: ①中位随访1 050(4~4 988)d,3年OS率、DFS率分别为(66.6±4.1)%、(63.3±4.1)%,3年累积RR率、NRM分别为(13.9±0.1)%、(22.2±0.1)%。②单因素分析显示,发生Ⅲ~Ⅳ度急性移植物抗宿主病(aGVHD)、造血干细胞移植合并症指数(HCT-CI)≥2分组和修订的国际预后积分系统(IPSS-R)极高危组的OS率均显著降低[(42.9±13.2)%对(72.9±4.2)%,χ(2)=8.620,P=0.003;(53.3±7.6)%对(72.6±4.7)%,χ(2)=6.681,P=0.010;(53.8±6.8)%对(76.6±6.2)%、(73.3±7.7)%,χ(2)=6.337,P=0.042]。MDS伴有原始细胞过多-2(MDS-EB2)和MDS转化急性髓系白血病(MDS-AML)患者,移植前接收化疗或去甲基化治疗不改善OS[(60.4±7.8)%对(59.2±9.6)%,χ(2)=0.042,P=0.838]。③多因素分析显示,HCT-CI是影响移植后OS和DFS的独立危险因素(P=0.012,HR=2.108,95%CI 1.174~3.785;P=0.008,HR=2.128,95%CI 1.219~3.712)。 结论: HCT-CI评价MDS患者移植后预后优于IPSS-R预后分组;发生Ⅲ~Ⅳ度aGVHD是影响移植后OS的不良预后因素;MDS-EB2和MDS-AML患者可以不化疗直接行MSD-PBSCT。.

Keywords: Hematopoietic stem cell transplantation; Myelodysplastic syndromes; Prognostic factors; Sibling donor.

MeSH terms

  • Graft vs Host Disease*
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Leukemia, Myeloid, Acute*
  • Myelodysplastic Syndromes*
  • Retrospective Studies
  • Siblings
  • Transplantation Conditioning
  • Transplantation, Homologous