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急性淋巴细胞白血病患儿孤立性髓外复发:化疗与骨髓移植治疗结果的比较。BFM复发研究组

Isolated extramedullary relapse in children with acute lymphoblastic leukemia: a comparison between treatment results of chemotherapy and bone marrow transplantation. BFM Relapse Study Group.

作者信息

Borgmann A, Hartmann R, Schmid H, Klingebiel T, Ebell W, Göbel U, Peters C, Gadner H, Henze G

机构信息

University Medical Center Rudolf Virchow, Free University of Berlin, Department of Pediatric Hematology and Oncology, Germany.

出版信息

Bone Marrow Transplant. 1995 Apr;15(4):515-21.

PMID:7655375
Abstract

The purpose of this study was to determine the therapeutic efficacy of different treatment strategies, namely chemotherapy, allogeneic and autologous bone marrow transplantation (BMT), for extramedullary relapse of acute lymphoblastic leukemia (ALL) in children in second or subsequent remission. Between 1983 and 1993, 165 patients up to 19 years of age with extramedullary relapse of ALL were registered in the multicenter ALL-REZ BFM trials. One hundred and thirty four children received chemotherapy only; 17 children were grafted from HLA-identical sibling donors 152 days (46-392 days) after diagnosis of relapse, and 14 children underwent autologous BMT after a median time of 137 (range 23-300) days. Event-free survival (EFS) at 5 years was 0.47 +/- 0.05 for patients receiving chemotherapy: 0.76 +/- 0.07 for late, 0.33 +/- 0.08 for early and 0.33 +/- 0.07 for very early relapsed patients. Sixty five patients are in complete remission (CR), 61 patients relapsed, 5 died from therapy related complications, 2 patients in CR were lost to follow-up and one patient developed a second malignancy. For patients who had undergone BMT, EFS at 5 years was 0.36 +/- 0.10 without significant difference between autologous BMT (8 of 14 in CR, 6 relapsed) and allogeneic BMT (6 of 17 in CR, 4 died of acute toxicity, and 7 relapsed).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究的目的是确定不同治疗策略,即化疗、异基因和自体骨髓移植(BMT),对儿童急性淋巴细胞白血病(ALL)第二次或后续缓解期髓外复发的治疗效果。1983年至1993年期间,165例19岁以下ALL髓外复发患者登记参加了多中心ALL-REZ BFM试验。134名儿童仅接受化疗;17名儿童在复发诊断后152天(46 - 392天)接受了来自HLA匹配同胞供者的移植,14名儿童在中位时间137天(范围23 - 300天)后接受了自体BMT。接受化疗患者的5年无事件生存率(EFS)为0.47±0.05:晚期复发患者为0.76±0.07,早期复发患者为0.33±0.08,极早期复发患者为0.33±0.07。65例患者完全缓解(CR),61例复发,5例死于治疗相关并发症,2例CR患者失访,1例发生第二恶性肿瘤。接受BMT的患者5年EFS为0.36±0.10,自体BMT(14例中8例CR,6例复发)和异基因BMT(17例中6例CR,4例死于急性毒性,7例复发)之间无显著差异。(摘要截短至250字)

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