Chemotherapy-Phased Imatinib Pulses Improve Long-Term Outcome of Adult Patients With Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia: Northern Italy Leukemia Group Protocol 09/00

被引:210
作者
Bassan, Renato [1 ]
Rossi, Giuseppe
Pogliani, Enrico M.
Di Bona, Eros
Angelucci, Emanuele
Cavattoni, Irene
Lambertenghi-Deliliers, Giorgio
Mannelli, Francesco
Levis, Alessandro
Ciceri, Fabio
Mattei, Daniele
Borlenghi, Erika
Terruzzi, Elisabetta
Borghero, Carlo
Romani, Claudio
Spinelli, Orietta
Tosi, Manuela
Oldani, Elena
Intermesoli, Tamara
Rambaldi, Alessandro
机构
[1] Osped Riuniti Bergamo, USC Ematol, I-24128 Bergamo, Italy
关键词
STEM-CELL TRANSPLANTATION; MINIMAL RESIDUAL DISEASE; TYROSINE KINASE INHIBITOR; POLYMERASE-CHAIN-REACTION; BLAST CRISIS; THERAPY; COMBINATION; APOPTOSIS; STI571; RESISTANCE;
D O I
10.1200/JCO.2010.28.1287
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Short imatinib pulses were added to chemotherapy to improve the long-term survival of adult patients with Philadelphia chromosome (Ph) -positive acute lymphoblastic leukemia (ALL), to optimize complete remission (CR) and stem-cell transplantation (SCT) rates. Patients and Methods Of 94 total patients (age range, 19 to 66 years), 35 represented the control cohort (ie, imatinib-negative [IM-negative] group), and 59 received imatinib 600 mg/d orally for 7 consecutive days (ie, imatinib-positive [IM-positive] group), starting from day 15 of chemotherapy course 1 and from 3 days before chemotherapy during courses 2 to 8. Patients in CR were eligible for allogeneic SCT or, alternatively, for high-dose therapy with autologous SCT followed by long-term maintenance with intermittent imatinib. Results CR and SCT rates were greater in the IM-positive group (CR: 92% v 80.5%; P = .08; allogeneic SCT: 63% v 39%; P = .041). At a median observation time of 5 years (range, 0.6 to 9.2 years), 22 patients in the IM-positive group versus five patients in the IM-negative group were alive in first CR (P = .037). Patients in the IM-positive group had significantly greater overall and disease-free survival probabilities (overall: 0.38 v 0.23; P = .009; disease free: 0.39 v 0.25; P = .044) and a lower incidence of relapse (P = .005). SCT-related mortality was 28% (ie, 15 of 54 patients), and postgraft survival probability was 0.46 overall. Conclusion This imatinib-based protocol improved long-term outcome of adult patients with Ph-positive ALL. With SCT, post-transplantation mortality and relapse remain the major hindrance to additional therapeutic improvement. Additional intensification of imatinib therapy should warrant a better molecular response and clinical outcome, both in patients selected for SCT and in those unable to undergo this procedure.
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页码:3644 / 3652
页数:9
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