Treatment-free remission after dasatinib in patients with chronic myeloid leukaemia in chronic phase with deep molecular response: Final 5-year analysis of DASFREE.


Journal

British journal of haematology
ISSN: 1365-2141
Titre abrégé: Br J Haematol
Pays: England
ID NLM: 0372544

Informations de publication

Date de publication:
09 2023
Historique:
revised: 05 04 2023
received: 07 02 2023
accepted: 27 04 2023
pmc-release: 01 09 2024
medline: 1 9 2023
pubmed: 29 5 2023
entrez: 29 5 2023
Statut: ppublish

Résumé

Patients with chronic myeloid leukaemia in chronic phase (CML-CP) who have a sustained deep molecular response (DMR) are eligible to discontinue treatment and attempt treatment-free remission (TFR). In the DASFREE study (ClinicalTrials.gov; NCT01850004), the 2-year TFR rate after dasatinib discontinuation was 46%; here we present the 5-year update. Patients with a stable DMR after ≥2 years of dasatinib therapy discontinued treatment and were followed for 5 years. At a minimum follow-up of 60 months, in 84 patients discontinuing dasatinib, the 5-year TFR rate was 44% (n = 37). No relapses occurred after month 39 and all evaluable patients who relapsed and restarted dasatinib (n = 46) regained a major molecular response in a median of 1.9 months. The most common adverse event during the off-treatment period was arthralgia (18%, 15/84); a total of 15 withdrawal events were reported in nine patients (11%). At the 5-year final follow-up, almost half of the patients who discontinued dasatinib after a sustained DMR maintained TFR. All evaluable patients who experienced a relapse quickly regained a DMR after restarting dasatinib, demonstrating that dasatinib discontinuation is a viable and potentially long-term option in patients with CML-CP. The safety profile is consistent with the previous report.

Identifiants

pubmed: 37246588
doi: 10.1111/bjh.18883
pmc: PMC10524617
mid: NIHMS1903454
doi:

Substances chimiques

Dasatinib RBZ1571X5H
Protein Kinase Inhibitors 0

Banques de données

ClinicalTrials.gov
['NCT01850004']

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

942-952

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA082103
Pays : United States

Informations de copyright

© 2023 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.

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Auteurs

Neil P Shah (NP)

UCSF School of Medicine, San Francisco, California, USA.

Valentín García-Gutiérrez (V)

Servicio Hematología y Hemoterapia, Hospital Universitario Ramón y Cajal, Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Madrid, Spain.

Antonio Jiménez-Velasco (A)

Servicio de Hematología y Hemoterapia, Hospital Regional Universitario de Málaga, IBIMA, Málaga, Spain.

Sarah M Larson (SM)

David Geffen School of Medicine at UCLA, Los Angeles, California, USA.

Susanne Saussele (S)

Medizinische Fakultät Mannheim der Universität Heidelberg, Mannheim, Germany.

Delphine Rea (D)

Adult Hematology Department, Hôpital Saint-Louis, Paris, France.

François-Xavier Mahon (FX)

Institut Bergonié Cancer Center, Université Bordeaux, Bordeaux, France.

Moshe Yair Levy (MY)

Baylor Charles A. Sammons Cancer Center, Dallas, Texas, USA.

María Teresa Gómez-Casares (MT)

Hospital Universitario de Gran Canaria Dr. Negrín, Las Palmas de Gran Canaria, Spain.

Michael J Mauro (MJ)

Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Oumar Sy (O)

Bristol Myers Squibb, Princeton, New Jersey, USA.

Patricia Martin-Regueira (P)

Bristol Myers Squibb, Princeton, New Jersey, USA.

Jeffrey H Lipton (JH)

Princess Margaret Cancer Centre, University of Toronto, Toronto, Ontario, Canada.

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Classifications MeSH