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首页> 外文期刊>Bone marrow transplantation >Effect of induced GVHD in leukemia patients relapsing after allogeneic bone marrow transplantation: single-center experience of 33 adult patients.
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Effect of induced GVHD in leukemia patients relapsing after allogeneic bone marrow transplantation: single-center experience of 33 adult patients.

机译:诱导的GVHD对同种异体骨髓移植后复发的白血病患者的影响:33名成人患者的单中心经验。

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In a retrospective single center study, we examined the outcome of induced GVHD in leukemia patients relapsing after allogeneic BMT. Thirty-three adult patients with leukemia (15 AML, 3 ALL, and 15 CML) persisting or relapsing 1-36 months (median, 6) after allogeneic BMT underwent various immune manipulations and consequently developed acute and/or chronic GVHD at our center. Immunotherapies to elicit GVHD comprised chemotherapy followed by PBSC (n = 18), non-myeloablative transplant (n = 2), PBL followed by IFN-alpha (n = 5), PBL alone (n = 3), abrupt cessation of CsA (n = 3), and CsA withdrawal combined with IFN-alpha (n = 2). Twenty-four (72.7%) patients obtained a remission including complete hematological or cytogenetic remission, respectively, for acute leukemias or CML. Overall survival of patients, estimated at 3 years using the Kaplan-Meier method, was 33.9% (95% CI, 20-52%). Twelve patients including two patients with ALL remain in complete hematological (n = 5) or cytogenetic remission (n = 7) 3-93 months (median 12) after achieving remission. Twelve (63.2%) of 19 dead patients died due to treatment-related toxicities; five patients from acute GVHD, three from GVHD followed by infections and four from infections. By multivariate Cox analysis, only chronic GVHD resulted in a higher probability of disease-free survival (P = 0.026). Eight patients who had both acute GVHD
机译:在一项回顾性单中心研究中,我们检查了同种异体BMT复发的白血病患者中诱导GVHD的结果。在同种异体BMT后持续或复发1-36个月(中位数为6)的33例成人白血病患者(15 AML,3 ALL和15 CML)经历了各种免疫操作,因此在我们中心发展为急性和/或慢性GVHD。引发GVHD的免疫疗法包括化学疗法,然后进行PBSC(n = 18),非清髓性移植(n = 2),PBL其次是IFN-alpha(n = 5),仅PBL(n = 3),突然终止CsA( n = 3),CsA退出与IFN-alpha结合(n = 2)。急性白血病或CML的缓解(包括完全血液学或细胞遗传学缓解)的患者为二十四名(72.7%)。使用Kaplan-Meier方法在3年时估计的患者总生存率为33.9%(95%CI,20-52%)。在达到缓解后,十二名患者(包括两名ALL患者)仍保持完全血液学(n = 5)或细胞遗传学缓解(n = 7)3-93个月(中位数12)。 19名死亡患者中有12名(63.2%)因与治疗有关的毒性而死亡;急性GVHD的5例患者,GVHD的3例,其次是感染,4例是感染。通过多变量Cox分析,只有慢性GVHD导致无病生存的可能性更高(P = 0.026)。急性I型GVHD和慢性GVHD的8例患者均未患白血病而活着。我们得出的结论是,同种异体BMT后,急性GVHD与相当大的毒性相关,而慢性GVHD在白血病复发中保持缓解。

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