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成年T细胞白血病/淋巴瘤患者的非亲属供者骨髓移植。

Bone marrow transplantation from unrelated donors for patients with adult T-cell leukaemia/lymphoma.

作者信息

Nakase K, Hara M, Kozuka T, Tanimoto K, Nawa Y

机构信息

Division of Hematology, Ehime Prefectural Central Hospital, Matsuyama City, Ehime, Japan.

出版信息

Bone Marrow Transplant. 2006 Jan;37(1):41-4. doi: 10.1038/sj.bmt.1705197.

Abstract

Adult T-cell leukaemia/lymphoma (ATLL) is a highly aggressive haematological malignancy. More than 40 cases of ATLL treated by allogeneic bone marrow transplantation (BMT) from sibling donors have been reported, while there have been only a few cases of unrelated BMT for treatment of this disease. We began performing allogeneic BMT from unrelated donors in 1999 to improve the outcome of ATLL patients with no suitable sibling donors. Eight ATLL patients underwent unrelated BMT; five received the conventional conditioning regimen consisting of cyclophosphamide and total body irradiation, while three received a reduced-intensity preparative regimen. Two patients died due to encephalopathy of unknown aetiology on days 10 and 35, and one patient died due to progression of ATLL 25 months after BMT. Five patients are currently alive and disease-free at a median of 20 months after BMT. Proviral human T-lymphotropic virus type-I (HTLV-I) DNA load in peripheral blood mononuclear cells (PBMCs) was assessed in four cases before and after BMT. HTLV-I proviral DNA load was reduced significantly after transplantation. Unrelated BMT is feasible for treatment of ATLL. Further studies in a larger number of cases are required to determine the optimal conditioning regimen and stem cell source.

摘要

成人T细胞白血病/淋巴瘤(ATLL)是一种侵袭性很强的血液系统恶性肿瘤。已有超过40例接受同胞供体异基因骨髓移植(BMT)治疗的ATLL病例报道,而采用无关供体BMT治疗该疾病的病例仅有少数。我们于1999年开始进行无关供体异基因BMT,以改善无合适同胞供体的ATLL患者的治疗效果。8例ATLL患者接受了无关供体BMT;5例接受了由环磷酰胺和全身照射组成的传统预处理方案,而3例接受了减低强度预处理方案。2例患者分别在第10天和第35天因病因不明的脑病死亡,1例患者在BMT后25个月因ATLL进展死亡。5例患者目前存活且无疾病,BMT后中位时间为20个月。对4例患者在BMT前后评估了外周血单个核细胞(PBMC)中的I型人嗜T淋巴细胞病毒(HTLV-I)前病毒DNA载量。移植后HTLV-I前病毒DNA载量显著降低。无关供体BMT治疗ATLL是可行的。需要对更多病例进行进一步研究,以确定最佳预处理方案和干细胞来源。

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