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

机译:成年T细胞白血病/淋巴瘤患者的无关供体的骨髓移植。

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摘要

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.
机译:成人T细胞白血病/淋巴瘤(ATLL)是一种高度侵袭性的血液恶性肿瘤。据报道,有40例来自同胞供体的同种异体骨髓移植(BMT)治疗的ATLL病例,而仅有少数几例无关的BMT病例用于治疗该疾病。我们从1999年开始从无关的供体中进行异基因BMT,以改善没有合适的同胞供体的ATLL患者的预后。 8例ATLL患者接受了无关的BMT;五名接受了由环磷酰胺和全身照射组成的常规调理方案,而三名接受了强度降低的制备方案。 BMT后25个月,有2例患者死于病因不明的脑病,而1例患者死于ATLL进展25个月。 BMT后中位数20个月,目前有5名患者活着并且没有疾病。在BMT之前和之后的4例患者中,评估了外周血单核细胞(PBMC)中的原人I型T淋巴细胞病毒(HTLV-1)DNA负荷。移植后,HTLV-1的前病毒DNA负载显着降低。无关的BMT对于ATLL的治疗是可行的。为了确定最佳的调节方案和干细胞来源,需要对大量病例进行进一步研究。

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