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Real‐world tyrosine kinase inhibitor treatment pathways, monitoring patterns and responses in patients with chronic myeloid leukaemia in the United Kingdom: the UK TARGET CML study

Milojkovic, Dragana; Cross, Nicholas C.P.; Ali, Sahra; Byrne, Jenny; Campbell, Gavin; Dignan, Fiona L.; Drummond, Mark; Huntly, Brian; Marshall, Scott; McMullin, Mary Frances; Neelakantan, Pratap; Raghavan, Manoj; Sivakumaran, Muttuswamy; Tighe, Jane; Wandroo, Farooq; Willis, Fenella; Glen, Fiona; Fildes, Louise; Collington, Sarah J.; Ryan, Jacqueline; Clark, Richard E.; Mead, Adam J.

Real‐world tyrosine kinase inhibitor treatment pathways, monitoring patterns and responses in patients with chronic myeloid leukaemia in the United Kingdom: the UK TARGET CML study Thumbnail


Authors

Dragana Milojkovic

Nicholas C.P. Cross

Sahra Ali

Jenny Byrne

Gavin Campbell

Fiona L. Dignan

Mark Drummond

Brian Huntly

Scott Marshall

Mary Frances McMullin

Pratap Neelakantan

Manoj Raghavan

Muttuswamy Sivakumaran

Jane Tighe

Farooq Wandroo

Fenella Willis

Fiona Glen

Louise Fildes

Sarah J. Collington

Jacqueline Ryan

Richard E. Clark

Adam J. Mead



Abstract

Management of chronic myeloid leukaemia (CML) has recently undergone dramatic changes, prompting the European LeukemiaNet (ELN) to issue recommendations in 2013; however, it remains unclear whether real-world CML management is consistent with these goals. We report results of UK TARGET CML, a retrospective observational study of 257 patients with chronic- phase CML prescribed a first-line TKI between 2013 and 2017, most of whom received first-line imatinib (n=203). Although 44% of patients required ≥1 change of TKI, these real-world data revealed that molecular assessments were frequently missed, 23% of patients with ELN-defined treatment failure did not switch TKI and kinase domain mutation analysis was performed in only 49% of patients who switched TKI for resistance. Major molecular response (MMR; BCR- ABL1IS ≤0.1%) and deep molecular response (DMR; BCR-ABL1IS ≤0.01%) were observed in 50% and 29%, respectively, of patients treated with first-line imatinib and 63% and 54% receiving a second-generation TKI first line. MMR and DMR were also observed in 77% and 44% of evaluable patients with ≥13 months’ follow-up receiving a second-generation TKI second line. We found little evidence that cardiovascular risk factors were considered during TKI management. These findings highlight key areas for improvement in providing optimal care to patients with CML.

Citation

Milojkovic, D., Cross, N. C., Ali, S., Byrne, J., Campbell, G., Dignan, F. L., …Mead, A. J. (2021). Real‐world tyrosine kinase inhibitor treatment pathways, monitoring patterns and responses in patients with chronic myeloid leukaemia in the United Kingdom: the UK TARGET CML study. British Journal of Haematology, 192(1), 62-74. https://doi.org/10.1111/bjh.16733

Journal Article Type Article
Acceptance Date Apr 20, 2020
Online Publication Date May 24, 2020
Publication Date 2021-01
Deposit Date May 20, 2020
Publicly Available Date May 25, 2021
Journal British Journal of Haematology
Print ISSN 0007-1048
Electronic ISSN 1365-2141
Publisher Wiley
Peer Reviewed Peer Reviewed
Volume 192
Issue 1
Pages 62-74
DOI https://doi.org/10.1111/bjh.16733
Keywords Hematology
Public URL https://nottingham-repository.worktribe.com/output/4475314
Publisher URL https://onlinelibrary.wiley.com/doi/abs/10.1111/bjh.16733
Additional Information This is the peer reviewed version of the following article: Milojkovic, D., Cross, N.C.P., Ali, S., Byrne, J., Campbell, G., Dignan, F.L., Drummond, M., Huntly, B., Marshall, S., McMullin, M.F., Neelakantan, P., Raghavan, M., Sivakumaran, M., Tighe, J., Wandroo, F., Willis, F., Glen, F., Fildes, L., Collington, S.J., Ryan, J., Clark, R.E. and Mead, A.J. (2020), Real‐world tyrosine kinase inhibitor treatment pathways, monitoring patterns and responses in patients with chronic myeloid leukaemia in the United Kingdom: the UK TARGET CML study. Br J Haematol., which has been published in final form at https://doi.org/10.1111/bjh.16733. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.

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