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成人急性淋巴细胞白血病的巩固治疗:一项前瞻性随机试验,比较异基因与自体骨髓移植,并检测自体骨髓移植后重组白细胞介素-2的影响。BGMT研究组。

Consolidation treatment of adult acute lymphoblastic leukemia: a prospective, randomized trial comparing allogeneic versus autologous bone marrow transplantation and testing the impact of recombinant interleukin-2 after autologous bone marrow transplantation. BGMT Group.

作者信息

Attal M, Blaise D, Marit G, Payen C, Michallet M, Vernant J P, Sauvage C, Troussard X, Nedellec G, Pico J

机构信息

Department of Hematology, Hôpital Purpan, Toulouse, France.

出版信息

Blood. 1995 Aug 15;86(4):1619-28.

PMID:7632972
Abstract

A prospective, randomized trial was initiated in adult acute lymphoblastic leukemia (ALL) to compare (1) disease-free survival (DFS) after allogeneic or autologous bone marrow transplantation (BMT) and (2) the relapse rate of patients treated with or without interleukin-2 (IL-2) after autologous BMT. A total of 135 previously untreated patients, aged under 55 years, received the Berlin-Frankfurt-Muster (BFM) induction regimen: 126 patients (93%), of which 120 were HLA-typed, achieved complete remission (CR). According to this genetic randomization, patients with (n = 43) or without an HLA-identical sibling (n = 77) were to receive allogeneic or autologous BMT, respectively. The 3-year post-CR probability of DFS was significantly higher in the HLA-identical sibling group than in the non-HLA-identical sibling group (68% v 26%; P < .001). Eligible patients were randomized to receive (n = 30) or not to receive (n = 30) IL-2 after autologous BMT: the 3-year post-BMT probability of continuous CR was similar in both groups (29% v 27%, respectively). We conclude that, in ALL, early allogeneic BMT after the BFM induction regimen is an effective consolidation treatment and that IL-2 does not decrease the high relapse rate observed after autologous BMT.

摘要

一项针对成人急性淋巴细胞白血病(ALL)的前瞻性随机试验启动,旨在比较:(1)异基因或自体骨髓移植(BMT)后的无病生存期(DFS);(2)自体BMT后接受或未接受白细胞介素-2(IL-2)治疗的患者的复发率。共有135例年龄在55岁以下、先前未接受过治疗的患者接受了柏林-法兰克福-明斯特(BFM)诱导方案:126例患者(93%)达到完全缓解(CR),其中120例进行了HLA分型。根据这种基因随机分组,有HLA相同同胞的患者(n = 43)或无HLA相同同胞的患者(n = 77)分别接受异基因或自体BMT。CR后3年的DFS概率在HLA相同同胞组显著高于非HLA相同同胞组(68%对26%;P <.001)。符合条件的患者在自体BMT后被随机分为接受(n = 30)或不接受(n = 30)IL-2治疗:两组BMT后3年持续CR的概率相似(分别为29%对27%)。我们得出结论,在ALL中,BFM诱导方案后早期进行异基因BMT是一种有效的巩固治疗方法,且IL-2不会降低自体BMT后观察到的高复发率。

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