首页> 外文期刊>Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation >Transplantation in remission improves the disease-free survival of patients with advanced myelodysplastic syndromes treated with myeloablative T cell-depleted stem cell transplants from HLA-identical siblings.
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Transplantation in remission improves the disease-free survival of patients with advanced myelodysplastic syndromes treated with myeloablative T cell-depleted stem cell transplants from HLA-identical siblings.

机译:缓解期移植可改善患有贫血的T细胞的干细胞移植(来自HLA相同的兄弟姐妹)治疗的晚期骨髓增生异常综合症患者的无病生存率。

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摘要

From 1985 to 2004, 49 patients with advanced myelodysplastic syndromes (MDS) (> or =5% blasts) or acute myeloid leukemia (AML) transformed from MDS underwent T cell depleted bone marrow or peripheral blood hematopoietic stem cell transplantation (HSCT) from HLA-identical siblings following conditioning with a myeloablative regimen that included total body irradiation (44 patients) or busulfan (5 patients). Thirty-six patients received chemotherapy (3 low dose and 33 induction doses) before conditioning, and 13 patients did not receive any chemotherapy. Prior to transplantation, 22 of the 36 treated patients were in hematologic remission; 4 were in a second refractory cytopenia phase (26 responders); 8 had failed to achieve remission; and 2 of the responders had progression or relapse of their MDS (10 failures). No post-transplantation pharmacologic prophylaxis for graft-versus-host disease (GVHD) was given. The median age was 48 yrs (range 13-61). Forty-five of the 49 patients engrafted; 2 had primary graft failure; and 2 died before engraftment. Only 3 patients developed acute GVHD (aGVHD) (grades I and III) and 1 chronic GVHD (cGVHD). At 3 yrs post-transplantation, the overall survival (OS) was 54% in the responders; 31% in the untreated group; and 0% in the failure group (P=.0004). The disease free survival (DFS) was 50%, 15% and 0% in each group respectively (P=.0008). In multivariate analysis, disease status before cytoreduction remained highly correlated with DFS (P<.001). The cumulative incidence (CI) of relapse at 2-yrs post-transplantation for the responders was 23%; for the untreated group was 38%; and for the failures was 50%. The CI of non-relapse mortality at 2-yrs post-transplantation, for the responders was 23%; for the untreated group was 38%; and for the failures was 40%. All survivors achieved a Karnofsky Performance Status (KPS) of > or =90. These results indicate that patients with advanced MDS who achieve and remain in remission or a second refractory cytopenia phase with chemotherapy before conditioning can achieve successful long-term remissions following a myeloablative T cell depleted allogeneic HSCT.
机译:从1985年到2004年,对49例由MDS转化为晚期骨髓增生异常综合征(MDS)(>或= 5%胚细胞)或急性髓细胞性白血病(AML)的患者进行了HLA的T细胞去除骨髓或外周血造血干细胞移植(HSCT) -采取包括全身体照射(44例)或白消安(5例)的清髓疗法调理后的同胞。 36例患者在调理前接受了化疗(3次低剂量和33次诱导剂量),而13例患者未接受任何化疗。移植前,在36位接受治疗的患者中,有22位处于血液学缓解状态。 4例处于第二难治性血细胞减少症阶段(26名反应者); 8名未达到缓解;和2位回应者的MDS进展或复发(10次失败)。没有针对移植物抗宿主病(GVHD)的移植后药理预防措施。中位年龄为48岁(范围13-61)。 49例患者中有45例; 2例发生原发性移植失败;有2人在嫁接前死亡。仅3例患者出现了急性GVHD(aGVHD)(I和III级)和1例慢性GVHD(cGVHD)。移植后3年,应答者的总生存率(OS)为54%;未治疗组为31%;失败组中为0%(P = .0004)。每组的无病生存率(DFS)分别为50%,15%和0%(P = .0008)。在多变量分析中,细胞减少前的疾病状态与DFS仍然高度相关(P <.001)。应答者在移植后2年时复发的累积发生率(CI)为23%;未治疗组为38%;失败率为50%。对于有反应者,移植后2年的非复发死亡率的CI为23%;未治疗组为38%;失败率为40%。所有幸存者的Karnofsky绩效状态(KPS)≥90。这些结果表明,晚期MDS患者在调理之前达到并保持缓解状态或通过化疗接受第二次难治性血细胞减少症阶段治疗后,可在清髓性T细胞清除异体造血干细胞移植后获得成功的长期缓解。

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