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Dasatinib discontinuation in patients with chronic-phase chronic myeloid leukemia and stable deep molecular response: the DASFREE study

Authors :
Franck-Emmanuel Nicolini
Oumar Sy
María Teresa Gómez-Casares
Fabrizio Pane
Sarah Larson
Jeffrey H. Lipton
Moshe Yair Levy
Delphine Rea
Susanne Saussele
Patricia Martin-Regueira
Neil P. Shah
Michael J. Mauro
Valentín García-Gutiérrez
Antonio Jiménez-Velasco
Francois-Xavier Mahon
Shah, Neil P
García-Gutiérrez, Valentín
Jiménez-Velasco, Antonio
Larson, Sarah
Saussele, Susanne
Rea, Delphine
Mahon, François-Xavier
Levy, Moshe Yair
Gómez-Casares, María Teresa
Pane, Fabrizio
Nicolini, Franck-Emmanuel
Mauro, Michael J
Sy, Oumar
Martin-Regueira, Patricia
Lipton, Jeffrey H
Source :
Leukemia & Lymphoma. 61:650-659
Publication Year :
2019
Publisher :
Informa UK Limited, 2019.

Abstract

Treatment-free remission (TFR) in patients with chronic myeloid leukemia in chronic phase (CML-CP) is considered a feasible option, especially with the ability of second-generation tyrosine kinase inhibitors to induce higher rates of sustained deep molecular response (DMR). DASFREE is an open-label, single-arm, multicenter phase II trial assessing TFR after dasatinib discontinuation in patients with CML-CP (N = 84). At 2 years, TFR was 46% in all patients. Multivariate analyses revealed statistically significant associations between 2-year TFR and duration of prior dasatinib (≥median; p = .0051), line of therapy (first line; p = .0138), and age (>65 years; p = .0012). No disease transformation occurred, and the most common adverse events experienced off treatment were musculoskeletal (observed in 30 patients); however, dasatinib withdrawal events were reported in nine patients (11%) by the investigator. Overall, these findings support the feasibility of discontinuing dasatinib for patients with CML-CP in sustained DMR in the first line and beyond.

Details

ISSN :
10292403 and 10428194
Volume :
61
Database :
OpenAIRE
Journal :
Leukemia & Lymphoma
Accession number :
edsair.doi.dedup.....cda44f1b02858fe9ff57aa2662f70337
Full Text :
https://doi.org/10.1080/10428194.2019.1675879