Tyrosine kinase inhibitor interruptions, discontinuations and switching in patients with chronic-phase chronic myeloid leukemia in routine clinical practice: SIMPLICITY
- PMID: 30290003
- PMCID: PMC6587733
- DOI: 10.1002/ajh.25306
Tyrosine kinase inhibitor interruptions, discontinuations and switching in patients with chronic-phase chronic myeloid leukemia in routine clinical practice: SIMPLICITY
Abstract
SIMPLICITY (NCT01244750) is an observational study exploring tyrosine kinase inhibitor (TKI) use and management patterns in patients with chronic phase-chronic myeloid leukemia in the US and Europe in routine clinical practice. Herein we describe interruptions, discontinuations and switching of TKI therapy during the initial 2 years of treatment among 1121 patients prospectively enrolled between October 1, 2010 and March 7, 2017. Patient characteristics were broadly similar between the imatinib (n = 370), dasatinib (n = 376), and nilotinib (n = 375) cohorts. Treatment interruptions occurred in 16.4% (year 1) and 4.0% (year 2) of patients, mainly attributed to hematologic intolerances. Treatment discontinuations occurred in 21.8% (year 1) and 10.2% (year 2) of patients, with the highest rate within the first 3 months for intolerance. Switching of TKI was seen in 17.8% (year 1) and 9.5% (year 2) of patients. Significant associations were found between TKI switching and female gender (year 1), age ≥65 years at diagnosis (year 2) and treatment with imatinib (year 2). Intolerance was the most common reason given for patients discontinuing and for switching TKI therapy; however resistance was also cited. Lack of response monitoring in routine clinical practice may have resulted in lower identification of resistance in this dataset. Data from SIMPLICITY suggest that, in routine clinical practice, intolerance and resistance to TKIs influence decisions to change treatment. Changes in TKI therapy are frequent, with nearly a third of patients discontinuing their first-line TKI.
© 2018 The Authors. American Journal of Hematology published by Wiley Periodicals, Inc.
Conflict of interest statement
RH has received consultancy fees from BMS and grants from Novartis. JC has received grants and/or consultancy fees from Ariad, BMS, Novartis, Pfizer and Teva. TZ, SG, and ID are employees of BMS. CGP has received grants and consultancy fees from BMS, and honoraria/grants from Pfizer. SLG has received grants and/or consultancy fees from BMS, Ariad, Novartis, and Pfizer. M Mauro has received grants from Novartis Oncology and Ariad/Takeda, and consultancy fees from BMS, Ariad/Takeda and Pfizer. M Michallet reports grants from BMS, consultant fees/honoraria from BMS, Pfizer, Novartis, Astellas Pharma, MSD and Genzyme. RP, BS, and LW declare no conflict of interest. AF and GS are employees of ICON Clinical Research.
Figures

Similar articles
-
Treatment patterns and clinical outcomes of tyrosine kinase inhibitors in chronic-phase CML in clinical practice: 3-year European SIMPLICITY data.Eur J Haematol. 2021 Jan;106(1):82-89. doi: 10.1111/ejh.13524. Epub 2020 Oct 9. Eur J Haematol. 2021. PMID: 32989776 Free PMC article.
-
Cross-Intolerance With Dasatinib Among Imatinib-Intolerant Patients With Chronic Phase Chronic Myeloid Leukemia.Clin Lymphoma Myeloma Leuk. 2016 Jun;16(6):341-349.e1. doi: 10.1016/j.clml.2016.03.004. Epub 2016 Mar 29. Clin Lymphoma Myeloma Leuk. 2016. PMID: 27133948
-
Efficacy and safety of nilotinib 300 mg twice daily in patients with chronic myeloid leukemia in chronic phase who are intolerant to prior tyrosine kinase inhibitors: Results from the Phase IIIb ENESTswift study.Leuk Res. 2018 Apr;67:109-115. doi: 10.1016/j.leukres.2018.02.013. Epub 2018 Feb 21. Leuk Res. 2018. PMID: 29494928 Clinical Trial.
-
Therapeutic drug monitoring of imatinib, nilotinib, and dasatinib for patients with chronic myeloid leukemia.Biol Pharm Bull. 2015;38(5):645-54. doi: 10.1248/bpb.b15-00103. Biol Pharm Bull. 2015. PMID: 25947908 Review.
-
Systematic Review and Meta-Analysis of -New-Generation Tyrosine Kinase Inhibitors versus Imatinib for Newly Diagnosed Chronic Myeloid Leukemia.Acta Haematol. 2020;143(3):204-216. doi: 10.1159/000501537. Epub 2019 Sep 12. Acta Haematol. 2020. PMID: 31514197
Cited by
-
Clinicohematological Spectrum of Chronic Myeloid Leukemia: A Cross-Sectional Study From a Tertiary Care Hospital in North India.Cureus. 2025 Jun 24;17(6):e86680. doi: 10.7759/cureus.86680. eCollection 2025 Jun. Cureus. 2025. PMID: 40709143 Free PMC article.
-
Comment on: "Switching TKIs during CML therapy is frequent, mostly driven by intolerance, and does not affect survival: a prospective Quebec registry study" by Busque et al.Blood Cancer J. 2025 Apr 19;15(1):70. doi: 10.1038/s41408-025-01288-8. Blood Cancer J. 2025. PMID: 40251176 Free PMC article. No abstract available.
-
Treatment patterns and clinical outcomes of tyrosine kinase inhibitors in chronic-phase CML in clinical practice: 3-year European SIMPLICITY data.Eur J Haematol. 2021 Jan;106(1):82-89. doi: 10.1111/ejh.13524. Epub 2020 Oct 9. Eur J Haematol. 2021. PMID: 32989776 Free PMC article.
-
Patterns of Tyrosine Kinase Inhibitor Utilization in Newly Treated Patients With Chronic Myeloid Leukemia: An Exhaustive Population-Based Study in France.Front Oncol. 2021 Sep 30;11:675609. doi: 10.3389/fonc.2021.675609. eCollection 2021. Front Oncol. 2021. PMID: 34660261 Free PMC article.
-
Molecular response and quality of life in chronic myeloid leukemia patients treated with intermittent TKIs: First interim analysis of OPTkIMA study.Cancer Med. 2021 Mar;10(5):1726-1737. doi: 10.1002/cam4.3778. Epub 2021 Feb 16. Cancer Med. 2021. PMID: 33594821 Free PMC article. Clinical Trial.
References
-
- Khoury HJ, Williams LA, Atallah E, Hehlmann R. Chronic myeloid leukemia: what every practitioner needs to know in 2017. American Society of Clinical Oncology educational book American Society of Clinical Oncology Meeting. 2017;37:468‐479. - PubMed
-
- National Comprehensive Cancer Network (NCCN) . NCCN Guidelines Chronic Myelogenous Leukemia Version 1. J Natl Compr Canc Netw. 2016;14:1505‐1512. - PubMed
Publication types
MeSH terms
Substances
Associated data
Grants and funding
LinkOut - more resources
Full Text Sources
Medical