Interruption or Discontinuation of Tyrosine Kinase Inhibitor Treatment in Chronic Myeloid Leukaemia: A Retrospective Cohort Study (SPARKLE) in Belgium.

Treatment interruption/discontinuation Chronic myeloid leukaemia Dasatinib Imatinib Molecular response Nilotinib Ponatinib Tyrosine kinase inhibitor 

Journal

Acta haematologica
ISSN: 1421-9662
Titre abrégé: Acta Haematol
Pays: Switzerland
ID NLM: 0141053

Informations de publication

Date de publication:
2019
Historique:
received: 28 05 2018
accepted: 01 03 2019
pubmed: 5 6 2019
medline: 18 3 2020
entrez: 5 6 2019
Statut: ppublish

Résumé

To assess interruptions/discontinuations of tyrosine kinase inhibitor (TKI) treatment in Belgian patients with chronic myeloid leukaemia (CML). This retrospective study included patients with TKI interruptions/discontinuations of ≥4 continuous weeks (no clinical trial context) between May 2013 and May 2016. Data collection took place between October 2016 and February 2017. All 60 participants (69 interruptions/discontinuations) had chronic-phase CML and 75% had at least a major molecular response (≥MMR) at interruption/discontinuation. Most interruptions/discontinuations occurred while on imatinib (36/69; 49%) and dasatinib (20/69; 29%). Most interruptions/discontinuations occurred due to side effects/intolerance (46/69; 67%); other reasons included a wish to conceive (6/69; 9%) and attempts to achieve treatment-free remission (TFR) (6/69; 9%). Interruptions due to side effects occurred later for imatinib- or dasatinib-treated patients than for those on nilotinib or ponatinib. Treatment was re-initiated in 62% (43/69) of cases. Most interruptions caused by side effects/intolerance were followed by treatment changes. All 4 patients with ≥MR 4.5 at interruption/discontinuation and ≥11-month follow-up who had not restarted treatment maintained the response. Although TKIs are used for long-term CML treatment, physicians sometimes recommend interruptions/discontinuations. In this study, interruptions/discontinuations were mainly caused by side effects or intolerance, rather than TFR attempts.

Identifiants

pubmed: 31163431
pii: 000499329
doi: 10.1159/000499329
doi:

Substances chimiques

Protein Kinase Inhibitors 0

Types de publication

Clinical Trial, Phase IV Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

197-207

Informations de copyright

© 2019 S. Karger AG, Basel.

Auteurs

Timothy Devos (T)

Hematology Department, University Hospitals Leuven, Leuven, Belgium, fabienne.jordens@novartis.com.

Gregor Verhoef (G)

Hematology Department, University Hospitals Leuven, Leuven, Belgium.

Eva Steel (E)

Universitair Ziekenhuis Ghent, Ghent, Belgium.

Dominiek Mazure (D)

Universitair Ziekenhuis Ghent, Ghent, Belgium.

Philippe Lewalle (P)

Institut Jules Bordet, Brussels, Belgium.

Dominique Bron (D)

Institut Jules Bordet, Brussels, Belgium.

Zwi Berneman (Z)

Universitair Ziekenhuis Antwerpen, Edegem, Belgium.

Fleur Samantha Benghiat (FS)

Hôpital Erasme, Brussels, Belgium.

Philippe Mineur (P)

Grand Hôpital de Charleroi (GHdC), Charleroi, Belgium.

Koen Theunissen (K)

Jessa Ziekenhuis, Campus Virga Jesse, Hasselt, Belgium.

Pierre Zachée (P)

Ziekenhuis Netwerk Antwerpen Stuivenberg, Antwerp, Belgium.

Chantal Doyen (C)

Centre Hospitalier Universitaire UCL Namur, Yvoir, Belgium.

Natalie Put (N)

Ziekenhuis Oost-Limburg, Campus Sint-Jan, Genk, Belgium.

Marie Lejeune (M)

Centre Hospitalier Universitaire de Liège, Liège, Belgium.

Koen Van Eygen (K)

AZ Groeninge, Campus Kennedylaan, Kortrijk, Belgium.

Violaine Havelange (V)

UCL Saint-Luc, Woluwe-Saint-Lambert, Belgium.

Michael Reusens (M)

Novartis Pharma NV/SA, Vilvoorde, Belgium.

Wim Pluymers (W)

Novartis Pharma NV/SA, Vilvoorde, Belgium.

Karen Peeters (K)

Novartis Pharma NV/SA, Vilvoorde, Belgium.

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Classifications MeSH