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

Renato Bassan(Associazione Italiana Ematologia Oncologia Pediatrica), Giuseppe Rossi(Associazione Italiana Ematologia Oncologia Pediatrica), Enrico Maria Pogliani(Associazione Italiana Ematologia Oncologia Pediatrica), Eros Di Bona(Associazione Italiana Ematologia Oncologia Pediatrica), Emanuele Angelucci(Associazione Italiana Ematologia Oncologia Pediatrica), Irene Cavattoni(Associazione Italiana Ematologia Oncologia Pediatrica), Giorgio Lambertenghi‐Deliliers(Associazione Italiana Ematologia Oncologia Pediatrica), Francesco Mannelli(Associazione Italiana Ematologia Oncologia Pediatrica), Alessandro Levis(Associazione Italiana Ematologia Oncologia Pediatrica), Fabio Ciceri(Associazione Italiana Ematologia Oncologia Pediatrica), Daniele Mattei(Associazione Italiana Ematologia Oncologia Pediatrica), Erika Borlenghi(Associazione Italiana Ematologia Oncologia Pediatrica), Elisabetta Terruzzi(Associazione Italiana Ematologia Oncologia Pediatrica), Carlo Borghero(Associazione Italiana Ematologia Oncologia Pediatrica), Claudio Romani(Associazione Italiana Ematologia Oncologia Pediatrica), Orietta Spinelli(Associazione Italiana Ematologia Oncologia Pediatrica), Manuela Tosi(Associazione Italiana Ematologia Oncologia Pediatrica), Elena Oldani(Associazione Italiana Ematologia Oncologia Pediatrica), Tamara Intermesoli(Associazione Italiana Ematologia Oncologia Pediatrica), Alessandro Rambaldi(Associazione Italiana Ematologia Oncologia Pediatrica)
Journal of Clinical Oncology
July 7, 2010
Cited by 274

Abstract

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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