PMID- 20606084 OWN - NLM STAT- MEDLINE DCOM- 20100818 LR - 20151119 IS - 1527-7755 (Electronic) IS - 0732-183X (Linking) VI - 28 IP - 22 DP - 2010 Aug 1 TI - 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. PG - 3644-52 LID - 10.1200/JCO.2010.28.1287 [doi] AB - 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. FAU - Bassan, Renato AU - Bassan R AD - U.S.C. Ematologia, Ospedali Riuniti, Bergamo, Italy. rbassan@ospedaliriuniti.bergamo.it FAU - Rossi, Giuseppe AU - Rossi G FAU - Pogliani, Enrico M AU - Pogliani EM FAU - Di Bona, Eros AU - Di Bona E FAU - Angelucci, Emanuele AU - Angelucci E FAU - Cavattoni, Irene AU - Cavattoni I FAU - Lambertenghi-Deliliers, Giorgio AU - Lambertenghi-Deliliers G FAU - Mannelli, Francesco AU - Mannelli F FAU - Levis, Alessandro AU - Levis A FAU - Ciceri, Fabio AU - Ciceri F FAU - Mattei, Daniele AU - Mattei D FAU - Borlenghi, Erika AU - Borlenghi E FAU - Terruzzi, Elisabetta AU - Terruzzi E FAU - Borghero, Carlo AU - Borghero C FAU - Romani, Claudio AU - Romani C FAU - Spinelli, Orietta AU - Spinelli O FAU - Tosi, Manuela AU - Tosi M FAU - Oldani, Elena AU - Oldani E FAU - Intermesoli, Tamara AU - Intermesoli T FAU - Rambaldi, Alessandro AU - Rambaldi A LA - eng PT - Controlled Clinical Trial PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20100706 PL - United States TA - J Clin Oncol JT - Journal of clinical oncology : official journal of the American Society of Clinical Oncology JID - 8309333 RN - 0 (Benzamides) RN - 0 (Piperazines) RN - 0 (Pyrimidines) RN - 8A1O1M485B (Imatinib Mesylate) SB - IM MH - Adult MH - Aged MH - Antineoplastic Combined Chemotherapy Protocols/*therapeutic use MH - Benzamides MH - Disease-Free Survival MH - Drug Administration Schedule MH - Female MH - Humans MH - Imatinib Mesylate MH - Italy MH - Male MH - Middle Aged MH - Piperazines/*administration & dosage MH - Precursor Cell Lymphoblastic Leukemia-Lymphoma/*drug therapy/mortality MH - Prognosis MH - Pyrimidines/*administration & dosage MH - Remission Induction MH - Stem Cell Transplantation EDAT- 2010/07/08 06:00 MHDA- 2010/08/19 06:00 CRDT- 2010/07/08 06:00 PHST- 2010/07/08 06:00 [entrez] PHST- 2010/07/08 06:00 [pubmed] PHST- 2010/08/19 06:00 [medline] AID - JCO.2010.28.1287 [pii] AID - 10.1200/JCO.2010.28.1287 [doi] PST - ppublish SO - J Clin Oncol. 2010 Aug 1;28(22):3644-52. doi: 10.1200/JCO.2010.28.1287. Epub 2010 Jul 6.