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 for Advanced Myelodysplastic Syndrome: Comparison of Outcomes between CD34(+) Selected and Unmodified Hematopoietic Stem Cell Transplantation
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Allogeneic Stem Cell Transplantation for Advanced Myelodysplastic Syndrome: Comparison of Outcomes between CD34(+) Selected and Unmodified Hematopoietic Stem Cell Transplantation

机译:双元性干细胞移植治疗晚期髓细胞增强综合征:CD34(+)选定与未改性造血干细胞移植的结果比较

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摘要

In this study, we compared transplantation outcomes of allogeneic hematopoietic stem cell transplantation (HSCT) in patients with advanced myelodysplastic syndrome (MDS) who received a CD34(+) cell-selected and those who received an unmodified allograft. This analysis initially included 181 patients, 60 who received a CD34(+) cell-selected transplant and 121 who received an unmodified transplant. Owing to significant differences in disease characteristics, the analysis was limited to patients with 10% blasts before HSCT (n = 145). Two groups were defined: low risk, with low- and intermediate-risk cytogenetics (CD34(+), n = 39; unmodified, n = 46), and high risk: poor and very poor risk cytogenetics (CD34(+), n = 19; unmodified, n = 41). In the low-risk group, the incidence of grade II-IV acute graft-versus-host disease (aGVHD) at 1 year post transplantation was 18% in the CD34(+) subgroup versus 41.3% in the unmodified subgroup (P =.015). There were no differences between the subgroups in the incidence of grade III-IV aGVHD. The incidence of chronic graft-versus-host disease (cGVHD) at 3 years in the 2 subgroups was 5.3% and 56%, respectively (P .001). At 3 years post-transplantation, relapse, overall survival (OS), and relapse-free survival (RFS) were similar in the CD34(+) and unmodified subgroups: 8.1% versus 19.4% (P=.187), 58.5% versus 53.7% (P=.51), and 59.5% versus 52.4% (P =.448). However, the composite outcome combining extensive cGVHD-free status and relapse-free status (CRFS) at 3 years was 59.5% in the CD34(+) group versus 19.2% in the unmodified group (P .001). In the high-risk group, grade II-IV aGVHD at 1 year was 31.6% in the CD34(+) subgroup versus 24.4% in the unmodified subgroup (P =.752). There were no differences between the subgroups in the incidence of grade III-IV aGVHD. The incidence of cGVHD at 3 years in the 2 subgroups was 0% versus 27.6% (P=.013). At 3 years post transplantation, relapse, OS, RFS, and CRFS in the 2 subgroups were 31.6% versus 69.3% (P =.007), 35.5% versus 14.5% (P =.068), 31.6% versus 10.7% (P =.045), and 31.6% versus 6.1% (P=.001), respectively. Cytogenetic abnormalities at diagnosis and transplant type had significant univariate associations with RFS in the high-risk cohort. Only cytogenetics (P =.03) remained associated with this outcome in a multivariate model. OS was similar in the 2 transplant groups; however, CRFS was superior in the CD34(+) cell-selected transplant group. (C) 2018 American Society for Blood and Marrow Transplantation.
机译:在本研究中,我们对接受CD34(+)细胞的先进骨髓增生综合征(MDS)患者进行了同种异体造血干细胞移植(HSCT)的移植效果。该分析最初包括181名患者,60名接受CD34(+)细胞选择的移植和121名接受未修改的移植的患者。由于疾病特征的显着差异,分析仅限于HSCT前10%患者的患者(n = 145)。定义两组:低风险,具有低和中等风险的细胞遗传学(CD34(+),n = 39;未修饰,n = 46),风险细胞遗传学差(CD34(+),n = 19;未修饰,n = 41)。在低风险组中,在未修饰的亚组的CD34(+)亚组中,在接生后1年后II-IV级急性移植术患者疾病(AGVHD)的发病率为18%(P =。 015)。亚组在III-IV级AGVHD的发生率之间没有差异。慢性移植物与 - 宿主疾病(CGVHD)在2个亚组3年内的发病率分别为5.3%和56%(P <.001)。在3年后移植后,复发,整体存活(OS)和无复发存活(RFS)在CD34(+)和未改性的亚组中相似:8.1%与19.4%(p = .187),58.5%与53.7%(p = .51)和59.5%对52.4%(p = .448)。然而,在未修饰基团的CD34(+)组与19.2%中,组合广泛的CGVHD地位和无复发状态(CRFS)的复合结果在3岁处为59.5%(P& .001)。在高风险群中,CD34(+)亚组1年的II-IV级AGVHD在未修改的亚组中为24.4%(P = .752)。亚组在III-IV级AGVHD的发生率之间没有差异。 2个亚组3年内CGVHD的发病率为0%,而27.6%(P = .013)。在3年后,2个亚组中的移植后,复发,OS,RFS和CRFs为31.6%,而69.3%(p = .007),35.5%对14.5%(p = .068),31.6%对10.7%(p = .045),分别为31.6%,分别与6.1%(p = .001)。诊断和移植型的细胞遗传学异常与高风险队列中的RFS具有重要的单变量联想。只有细胞遗传学(P = .03)仍然与多元模型中的这种结果相关联。 OS在2种移植组中类似;然而,CRF在CD34(+)细胞选择的移植组中优异。 (c)2018年美国血液和骨髓移植学会。

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