Superiority of allogeneic hematopoietic stem-cell transplantation compared with chemotherapy alone in high-risk childhood T-cell acute lymphoblastic leukemia: Results from ALL-BFM 90 and 95

被引:91
作者
Schrauder, Andre
Reiter, Alfred
Gadner, Helmut
Niethammer, Dietrich
Klingebiel, Thomas
Kremens, Bernhard
Peters, Christina
Ebell, Wolfram
Zimmermann, Martin
Niggli, Felix
Ludwig, Wolf-Dieter
Riehm, Hansjoerg
Welte, Karl
Schrappe, Martin
机构
[1] Univ Med Ctr Schleswig Holstein, Dept Pediat, D-24105 Kiel, Germany
[2] Univ Giessen, Dept Pediat Hematol & Oncol, Giessen, Germany
[3] Univ Tubingen Hosp, Dept Pediat Hematol & Oncol, Tubingen, Germany
[4] Goethe Univ Frankfurt, Dept Pediat Hematol & Oncol, D-6000 Frankfurt, Germany
[5] Univ Hosp, Dept Pediat Hematol & Oncol, Essen, Germany
[6] Univ Med Berlin, Dept Gen Pediat & Bone Marrow Transplantat, Charite, Berlin, Germany
[7] Hannover Med Sch, Dept Pediat Hematol & Oncol, D-3000 Hannover, Germany
[8] Helioc Clin Berlin Buch, Charite, Dept Hematol Oncol & Tumor Immunol, Robert Rossle Klin, Berlin, Germany
[9] St Anna Childrens Hosp, A-1090 Vienna, Austria
[10] Univ Zurich Hosp, Dept Pediat Hematol & Oncol, CH-8091 Zurich, Switzerland
关键词
BONE-MARROW-TRANSPLANTATION; MINIMAL RESIDUAL DISEASE; 2ND REMISSION; PEDIATRIC-PATIENTS; EARLY-DIAGNOSIS; 1ST REMISSION; UKALL X; CHILDREN; THERAPY; TRIALS;
D O I
10.1200/JCO.2006.06.2679
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose The role of hematopoietic stem-cell transplantation (SCT) in first complete remission (CR1) for children with very high-risk (VHR) acute lymphoblastic leukemia (ALL) is still under critical discussion. Patients and Methods In the ALL-Berlin-Frankfurt-Munster (BFM) 90 and ALL-BFM 95 trials, 387 patients were eligible for SCT if there was a matched sibling donor (MSD). T-cell ALL (T-ALL) patients with poor in vivo response to initial treatment represented the largest homogeneous subgroup within VHR patients. Results Of 191 high-risk (HR) T-ALL patients, 179 patients (94%) achieved CR1. Twenty-three patients received an MSD-SCT. Furthermore, in trial ALL-BFM 95, eight matched unrelated donors (MUDs) and five mismatched family donors (MMFDs) were used. The median time to SCT was 5 months (range, 2.4 to 10.8 months) from diagnosis. The 5-year disease-free survival (DFS) was 67% +/- 8% for 36 patients who received an SCT in CR1 and 42% +/- 5% for the 120 patients treated with chemotherapy alone having an event-free survival time of at least the median time to transplantation (Mantel-Byar, P = .01). Overall survival (OS) rate for the SCT group was 67% +/- 8% at 5 years, whereas patients treated with chemotherapy alone had an OS rate of 47% +/- 5% at 5 years (Mantel-Byar, P = .01). Outcome of patients who received MSD-SCT versus MUD-/MMFD-SCT was comparable (DFS, 65% +/- 10% v 69% +/- 13%, respectively). However, relapses only occurred after MSD-SCT (eight of 23 patients), whereas treatment-related mortality only occurred after MUD-/MMFD-SCT (four of 13 patients). Conclusion SCT in CR1 is superior to treatment with chemotherapy alone for childhood HR-T-ALL.
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收藏
页码:5742 / 5749
页数:8
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