Management of chronic myeloid leukaemia in clinical practice in France: results of the French subset of patients from the UNIC study
- PMID: 19961284
- DOI: 10.1185/03007990903479299
Management of chronic myeloid leukaemia in clinical practice in France: results of the French subset of patients from the UNIC study
Abstract
Objective: To assess real-life treatment practices with imatinib for chronic-phase chronic myeloid leukaemia (CP-CML) in France.
Research design and methods: In the observational 'Unmet Needs in CML' (UNIC) study of CML management in Europe, case report forms were completed retrospectively for eligible patients (> or =18 years of age, currently treated for CML) during enrolment (September 2006-March 2007). Results from the subset of patients from France are presented.
Main outcome measures: Primary objectives were to estimate from the collected data the proportions of patients ever treated with imatinib and those experiencing imatinib resistance and/or intolerance as determined by physicians' diagnoses of resistance/intolerance leading to a change in imatinib use. Collected data were analysed descriptively. Secondary descriptive measures included imatinib dose modifications and methods for treatment response monitoring.
Results: Of the 654 French CP-CML patients, 95.9% had received imatinib. Of these, 15% were judged by physicians as imatinib-resistant and 31% as imatinib-intolerant (not mutually exclusive) during treatment, 44% required dose modification and 23% discontinued imatinib. In the 12 months preceding the last observation, 65% had a cytogenetic features analysis and 93% had a polymerase chain reaction (PCR) assessment of molecular response. Importantly, and contrasting with European recommendations, 46% of imatinib-resistant patients had never been assessed for BCR-ABL mutations.
Limitations: The observational study design limits data collection and interpretation. The findings are specific to the French healthcare system and may not apply to other countries.
Conclusion: This observational study of CP-CML management in France confirmed that most patients are treated with imatinib, a treatment widely recognised as efficacious. The study highlights opportunities for optimising CML management, as a proportion of patients may require alternative treatment strategies due to imatinib resistance/intolerance. Response monitoring rates differ from recommendations, representing another opportunity for improving care for CP-CML patients through early identification of patients failing current therapy.
Similar articles
-
Dasatinib: from treatment of imatinib-resistant or -intolerant patients with chronic myeloid leukemia to treatment of patients with newly diagnosed chronic phase chronic myeloid leukemia.Clin Ther. 2012 Feb;34(2):272-81. doi: 10.1016/j.clinthera.2012.01.009. Epub 2012 Jan 27. Clin Ther. 2012. PMID: 22285209 Review.
-
Mutation status and clinical outcome of 89 imatinib mesylate-resistant chronic myelogenous leukemia patients: a retrospective analysis from the French intergroup of CML (Fi(phi)-LMC GROUP).Leukemia. 2006 Jun;20(6):1061-6. doi: 10.1038/sj.leu.2404236. Leukemia. 2006. PMID: 16642048
-
Not all imatinib resistance in CML are BCR-ABL kinase domain mutations.Ann Hematol. 2006 Dec;85(12):841-7. doi: 10.1007/s00277-006-0171-8. Epub 2006 Sep 28. Ann Hematol. 2006. PMID: 17006667 Clinical Trial.
-
Early reduction of BCR-ABL mRNA transcript levels predicts cytogenetic response in chronic phase CML patients treated with imatinib after failure of interferon alpha.Leukemia. 2002 Sep;16(9):1579-83. doi: 10.1038/sj.leu.2402680. Leukemia. 2002. PMID: 12200666 Clinical Trial.
-
Analysis of Bcr-Abl kinase domain mutations in Korean chronic myeloid leukaemia patients: poor clinical outcome of P-loop and T315I mutation is disease phase dependent.Hematol Oncol. 2009 Dec;27(4):190-7. doi: 10.1002/hon.894. Hematol Oncol. 2009. PMID: 19274615
Cited by
-
Cholesterol esterification inhibition and imatinib treatment synergistically inhibit growth of BCR-ABL mutation-independent resistant chronic myelogenous leukemia.PLoS One. 2017 Jul 18;12(7):e0179558. doi: 10.1371/journal.pone.0179558. eCollection 2017. PLoS One. 2017. PMID: 28719608 Free PMC article.
-
Dasatinib: a review of its use in the treatment of chronic myeloid leukaemia and Philadelphia chromosome-positive acute lymphoblastic leukaemia.Drugs. 2011 Sep 10;71(13):1771-95. doi: 10.2165/11207580-000000000-00000. Drugs. 2011. PMID: 21902298 Review.
-
Real-world efficacy and safety outcomes of imatinib treatment in patients with chronic myeloid leukemia: An Australian experience.Pharmacol Res Perspect. 2022 Oct;10(5):e01005. doi: 10.1002/prp2.1005. Pharmacol Res Perspect. 2022. PMID: 36106342 Free PMC article.
-
The role of observational studies in optimizing the clinical management of chronic myeloid leukemia.Ther Adv Hematol. 2015 Feb;6(1):3-14. doi: 10.1177/2040620714560305. Ther Adv Hematol. 2015. PMID: 25642311 Free PMC article. Review.
-
Tyrosine kinase inhibition: a therapeutic target for the management of chronic-phase chronic myeloid leukemia.Expert Rev Anticancer Ther. 2013 Dec;13(12):1433-52. doi: 10.1586/14737140.2013.859074. Expert Rev Anticancer Ther. 2013. PMID: 24236822 Free PMC article. Review.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous