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缓解期进行移植可提高接受来自 HLA 同型同胞的清髓性 T 细胞去除干细胞移植治疗的晚期骨髓增生异常综合征患者的无病生存率。

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.

作者信息

Castro-Malaspina Hugo, Jabubowski Ann A, Papadopoulos Esperanza B, Boulad Farid, Young James W, Kernan Nancy A, Perales Miguel A, Small Trudy N, Hsu Katharine, Chiu Michelle, Heller Glenn, Collins Nancy H, Jhanwar Suresh C, van den Brink Marcel, Nimer Stephen D, O'Reilly Richard J

机构信息

The Allogeneic Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.

出版信息

Biol Blood Marrow Transplant. 2008 Apr;14(4):458-68. doi: 10.1016/j.bbmt.2008.02.006.

Abstract

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.

摘要

1985年至2004年,49例晚期骨髓增生异常综合征(MDS)(原始细胞≥5%)或由MDS转化而来的急性髓系白血病(AML)患者,在接受包含全身照射(44例患者)或白消安(5例患者)的清髓方案预处理后,接受了来自 HLA 相合同胞的T细胞去除的骨髓或外周血造血干细胞移植(HSCT)。36例患者在预处理前接受了化疗(3例低剂量和33例诱导剂量),13例患者未接受任何化疗。移植前,36例接受治疗的患者中有22例处于血液学缓解状态;4例处于第二个难治性血细胞减少期(26例缓解者);8例未达到缓解;2例缓解者出现MDS进展或复发(10例未缓解者)。未进行移植后移植物抗宿主病(GVHD)的药物预防。中位年龄为48岁(范围13 - 61岁)。49例患者中有45例植入;2例发生原发性移植失败;2例在植入前死亡。仅3例患者发生急性GVHD(I级和III级),1例发生慢性GVHD(cGVHD)。移植后3年,缓解者的总生存率(OS)为54%;未治疗组为31%;未缓解组为0%(P = 0.0004)。无病生存率(DFS)在每组中分别为50%、15%和0%(P = .0008)。多因素分析中,细胞减少前的疾病状态与DFS仍高度相关(P < 0.001)。缓解者移植后2年复发的累积发生率(CI)为23%;未治疗组为38%;未缓解组为50%。缓解者移植后2年非复发死亡率的CI为23%;未治疗组为

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