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Final 3-year Results of the Dasatinib Discontinuation Trial in Patients With Chronic Myeloid Leukemia Who Received Dasatinib as a Second-line Treatment.

Authors :
Okada M
Imagawa J
Tanaka H
Nakamae H
Hino M
Murai K
Ishida Y
Kumagai T
Sato S
Ohashi K
Sakamaki H
Wakita H
Uoshima N
Nakagawa Y
Minami Y
Ogasawara M
Takeoka T
Akasaka H
Utsumi T
Uike N
Sato T
Ando S
Usuki K
Mizuta S
Hashino S
Nomura T
Shikami M
Fukutani H
Ohe Y
Kosugi H
Shibayama H
Maeda Y
Fukushima T
Yamazaki H
Tsubaki K
Kukita T
Adachi Y
Nataduka T
Sakoda H
Yokoyama H
Okamoto T
Shirasugi Y
Onishi Y
Nohgawa M
Yoshihara S
Morita S
Sakamoto J
Kimura S
Source :
Clinical lymphoma, myeloma & leukemia [Clin Lymphoma Myeloma Leuk] 2018 May; Vol. 18 (5), pp. 353-360.e1. Date of Electronic Publication: 2018 Mar 15.
Publication Year :
2018

Abstract

Introduction: We previously reported an interim analysis of the DADI (dasatinib discontinuation) trial. The results showed that 48% of patients with chronic myeloid leukemia in the chronic phase who maintained a deep molecular response (DMR) for ≥ 1 year could discontinue second- or subsequent-line dasatinib treatment safely at a median follow-up of 20 months. However, the results from longer follow-up periods would be much more useful from a clinical perspective.<br />Patients and Methods: The DADI trial was a prospective, multicenter trial conducted in Japan. After confirming a stable DMR for ≥ 1 year, dasatinib treatment subsequent to imatinib or nilotinib was discontinued. After discontinuation, the loss of DMR (even of 1 point) was defined as stringent molecular relapse, thereby triggering therapy resumption. The predictive factors of treatment-free remission (TFR) were analyzed.<br />Results: The median follow-up period was 44.0 months (interquartile range, 40.5-48.0 months). The estimated overall TFR rate at 36 months was 44.4% (95% confidence interval, 32.0%-56.2%). Only 2 patients developed a molecular relapse after the 1-year cutoff point. The presence of imatinib resistance was a significant risk factor for molecular relapse. Moreover, high natural killer cell and low γδ <superscript>+</superscript> T-cell and CD4 <superscript>+</superscript> regulatory T-cell (CD25 <superscript>+</superscript> CD127 <superscript>low</superscript> ) counts before discontinuation correlated significantly with successful therapy discontinuation.<br />Conclusion: These findings suggest that discontinuation of second- or subsequent-line dasatinib after a sustained DMR of ≥ 1 year is feasible, especially for patients with no history of imatinib resistance. In addition, the natural killer cell count was associated with the TFR.<br /> (Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
2152-2669
Volume :
18
Issue :
5
Database :
MEDLINE
Journal :
Clinical lymphoma, myeloma & leukemia
Publication Type :
Academic Journal
Accession number :
29610029
Full Text :
https://doi.org/10.1016/j.clml.2018.03.004