Patient- and physician-reported pain after tyrosine kinase inhibitor discontinuation among patients with chronic myeloid leukemia.


Journal

Haematologica
ISSN: 1592-8721
Titre abrégé: Haematologica
Pays: Italy
ID NLM: 0417435

Informations de publication

Date de publication:
01 11 2022
Historique:
received: 17 11 2021
pubmed: 6 5 2022
medline: 4 11 2022
entrez: 5 5 2022
Statut: epublish

Résumé

For patients with optimally treated chronic myeloid leukemia (CML), discontinuation of tyrosine kinase inhibitor (TKI) therapy can lead to treatment-free remission. In previous trials, TKI discontinuation has been associated with increased musculoskeletal pain in some patients ("withdrawal syndrome"), based on physician-reported adverse events (AE). Patient-reported pain has not been described. The Life After Stopping TKI study was a 14-site prospective, non-randomized clinical trial of TKI discontinuation. We defined increased pain after discontinuation as: (i) a physician-reported pain AE, (ii) a 2-level increase in self-reported musculoskeletal pain (4-level single item), or (iii) initiation of a medication for pain. We plotted the trajectory of patient-reported pain over time using a piecewise mixed-effects ordinal logistic model. Within 3 months of discontinuation, 35 of 172 patients (20.3%) had a physician-reported pain AE, 22 of 172 (12.8%) had an increase in self-reported pain, and 18 of 154 (11.7%) initiated a pain medication. Agreement among these measures was limited; overall, 60 of 172 patients (34.9%) had increased pain. Three patients (1.7%) restarted a TKI because of pain. The modelpredicted trajectory showed an increase in pain in the first 3 months followed by a decrease, returning to baseline levels by 6 months and further decreasing after that. This trajectory was similar among patients who did and did not restart TKI, suggesting that resuming a TKI for withdrawal syndrome may be necessary for some, but other approaches to manage pain should be tried so that patients can remain in treatment-free remission when possible.

Identifiants

pubmed: 35511672
doi: 10.3324/haematol.2021.280377
pmc: PMC9614525
doi:

Substances chimiques

Protein Kinase Inhibitors 0

Types de publication

Clinical Trial Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

2641-2649

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA184798
Pays : United States

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Auteurs

Kathryn E Flynn (KE)

Medical College of Wisconsin, Milwaukee, WI. kflynn@mcw.edu.

Ehab Atallah (E)

Medical College of Wisconsin, Milwaukee, WI.

Li Lin (L)

Duke University School of Medicine, Durham, NC.

Neil P Shah (NP)

University of California at San Francisco, San Francisco, CA.

Richard T Silver (RT)

Weill Cornell Medicine, New York, NY.

Richard A Larson (RA)

University of Chicago, Chicago, IL.

Javier Panilla-Ibarz (J)

H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.

James E Thompson (JE)

Roswell Park Comprehensive Cancer Center, Buffalo, NY.

Vivian G Oehler (VG)

Fred Hutchinson Cancer Research Center, Seattle, WA.

Jerald P Radich (JP)

Fred Hutchinson Cancer Research Center, Seattle, WA.

Vamsi Kota (V)

Georgia Cancer Center at Augusta University, Augusta, GA.

Michael J Mauro (MJ)

Memorial Sloan Kettering Cancer Center, New York, NY.

Charles A Schiffer (CA)

Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI.

Jorge Cortes (J)

Georgia Cancer Center at Augusta University, Augusta, GA.

Kevin P Weinfurt (KP)

Duke University School of Medicine, Durham, NC.

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Classifications MeSH