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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

Authors :
Giorgio Lambertenghi-Deliliers
Carlo Borghero
Renato Bassan
Giuseppe Rossi
Claudio Romani
Tamara Intermesoli
Elisabetta Terruzzi
Erika Borlenghi
Orietta Spinelli
Enrico Pogliani
Fabio Ciceri
Alessandro Levis
Irene Cavattoni
Emanuele Angelucci
Francesco Mannelli
Manuela Tosi
Eros Di Bona
Daniele Mattei
Elena Oldani
Alessandro Rambaldi
Bassan, R
Rossi, G
Pogliani, Em
Di Bona, E
Angelucci, E
Cavattoni, I
Lambertenghi Deliliers, G
Mannelli, F
Levis, A
Ciceri, Fabio
Mattei, D
Borlenghi, E
Terruzzi, E
Borghero, C
Romani, C
Spinelli, O
Tosi, M
Oldani, E
Intermesoli, T
Rambaldi, A.
Pogliani, E
Ciceri, F
Rambaldi, A
Source :
Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 28(22)
Publication Year :
2010

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.

Details

ISSN :
15277755
Volume :
28
Issue :
22
Database :
OpenAIRE
Journal :
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Accession number :
edsair.doi.dedup.....3ab0a62c1d60117a426e13abfeb1e66b