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Long-term follow-up of de novo chronic phase chronic myelogenous leukemia patients on front-line imatinib.

Authors :
Nicolini FE
Alcazer V
Cony-Makhoul P
Heiblig M
Morisset S
Fossard G
Bidet A
Schmitt A
Sobh M
Hayette S
Mahon FX
Dulucq S
Etienne G
Source :
Experimental hematology [Exp Hematol] 2018 Aug; Vol. 64, pp. 97-105.e4. Date of Electronic Publication: 2018 May 23.
Publication Year :
2018

Abstract

For the last 15years, imatinib mesylate (IM) has represented the gold standard treatment for chronic-phase chronic myelogenous leukemia (CP-CML); however, outcomes in the very long term remain unknown. We retrospectively analyzed the outcome of 418 IM first-line treated CP-CML patients followed in three reference centers over 15years in and outside of clinical trials, which is believed to represent the "real-life" care of such patients. Molecular analyses were standardized over the years. In case of intolerance or resistance or IM cessation and progression, all clinical data were collected and analyzed. After a median follow-up of 83 months (range 1-194), the overall survival (OS) rates were 91% and 82%, the progression-free survival (PFS) rates were 88.5% and 81%, and the event-free survival rates, including switching to another tyrosine kinase inhibitor, were 65% and 51%, respectively, at 5 and 10years. Thirteen patients (3%) entered blast crisis (BC) with a median survival of 2.2years after BC onset. Forty-nine percent of patients were in major molecular response at 1 year. Univariate analysis failed to detect any impact on survival of molecular response at 3 and 6 months. Sokal score had a significant impact on OS and PFS in a Cox model. Age had a significant impact on OS and PFS, mainly due to deaths in elderly patients unrelated to CML. Overall, 21% of patients reached a stable (≥1 year) molecular response 4 (MR4) and 6.5% reached MR4.5. At last follow-up, 63% of patients were still on IM and 19% were in treatment-free remission. We conclude that IM is an excellent therapeutic option providing impressive long-term OS rates.<br /> (Copyright © 2018 ISEH -- Society for Hematology and Stem Cells. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1873-2399
Volume :
64
Database :
MEDLINE
Journal :
Experimental hematology
Publication Type :
Academic Journal
Accession number :
29800673
Full Text :
https://doi.org/10.1016/j.exphem.2018.05.003