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异基因骨髓移植在首次缓解的青少年或成年急性淋巴细胞白血病或淋巴细胞淋巴瘤患者中的作用。

Role of allogenic bone marrow transplantation in adolescent or adult patients with acute lymphoblastic leukaemia or lymphoblastic lymphoma in first remission.

作者信息

De Witte T, Awwad B, Boezeman J, Schattenberg A, Muus P, Raemaekers J, Preijers F, Strijckmans P, Haanen C

机构信息

Department of Internal Medicine, University Hospital St. Radboud, Nijmegen, The Netherlands.

出版信息

Bone Marrow Transplant. 1994 Nov;14(5):767-74.

PMID:7889010
Abstract

Sixty-nine adolescents and adults 15-51 years of age with untreated acute lymphoblastic leukaemia (ALL, 54 patients) or lymphoblastic lymphoma (LL, 15 patients) were referred for intensive antileukaemic therapy. Patients were treated according to one of two protocols. Both included induction and consolidation with vincristine, prednisone, daunorubicin, cyclophosphamide, Ara C and asparaginase. Fifty-eight patients achieved complete remission within 8 weeks of chemotherapy. One additional patient entered remission after allogeneic BMT. Altogether 86% of the patients achieved CR. Thirty-three patients are alive, corresponding to an actuarial survival of 48 +/- 6% at 5 years after start of therapy. Survival from time of achievement of CR is 53 +/- 7% at 5 years and disease-free survival (DFS) is 52 +/- 7%. Consolidation treatment was given to all patients except one. An HLA-identical sibling was identified for 30 patients (45%). Twenty-two patients were scheduled to be transplanted with marrow from an HLA-identical sibling. The survival and DFS in these 22 patients was 58 +/- 11% at 5 years. DFS was not significantly different compared with the DFS of the eight patients who received an auto-BMT and the 26 patients treated with maintenance chemotherapy. DFS at 5 years was 63 +/- 17% and 40 +/- 10%, respectively. We also evaluated the influence of the presence of an HLA-identical sibling on the treatment outcome of all patients alive 12 weeks after initiation of remission-induction therapy.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

69名年龄在15至51岁之间未经治疗的急性淋巴细胞白血病(ALL,54例患者)或淋巴细胞淋巴瘤(LL,15例患者)的青少年及成人被转诊接受强化抗白血病治疗。患者根据两种方案之一进行治疗。两种方案均包括使用长春新碱、泼尼松、柔红霉素、环磷酰胺、阿糖胞苷和天冬酰胺酶进行诱导和巩固治疗。58例患者在化疗8周内达到完全缓解。另有1例患者在异基因骨髓移植后进入缓解期。总共有86%的患者达到完全缓解(CR)。33例患者存活,相当于治疗开始后5年的精算生存率为48±6%。从达到CR时起计算,5年生存率为53±7%,无病生存率(DFS)为52±7%。除1例患者外,所有患者均接受了巩固治疗。为30例患者(45%)找到了HLA相同的同胞。22例患者计划接受来自HLA相同同胞捐献者的骨髓移植。这22例患者5年时的生存率和DFS为58±11%。与接受自体骨髓移植的8例患者和接受维持化疗的26例患者的DFS相比,差异无统计学意义。5年时的DFS分别为63±17%和40±10%。我们还评估了HLA相同同胞的存在对诱导缓解治疗开始12周后所有存活患者治疗结局的影响。(摘要截短至250字)

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