Outcome of Imatinib Treatment in Yemeni Patients With Chronic Myeloid Leukemia and the Influence of Nonadherence to Treatment and Duration of Previous Hydroxyurea Therapy.


Journal

Clinical lymphoma, myeloma & leukemia
ISSN: 2152-2669
Titre abrégé: Clin Lymphoma Myeloma Leuk
Pays: United States
ID NLM: 101525386

Informations de publication

Date de publication:
03 2020
Historique:
received: 24 10 2019
revised: 17 11 2019
accepted: 18 11 2019
pubmed: 28 1 2020
medline: 15 5 2021
entrez: 28 1 2020
Statut: ppublish

Résumé

In a developing country like Yemen, data are limited regarding the outcome of imatinib treatment of chronic myeloid leukemia and the effect of nonadherence to imatinib treatment and previous duration of hydroxyurea treatment. A longitudinal cohort study, which included 164 Yemeni patients, was performed. Data regarding the disease characteristics, adherence to treatment (the medication possession ratio) and outcome were analyzed. After a median follow-up of 60 months and a median duration of imatinib treatment of 46 months, 79 (48.2%) patients were adherent to treatment. In adherent patients, the overall survival and progression-free survival (PFS) were 78 (98.7%) and 73 patients (92.4%), respectively and major molecular response (MMR) rates at 12 months and at 46 months were 32 (41.0%) and 45 patients (57.0%), respectively, compared with 67 (78.8%), 51 (60%), 5 (6.9%), and 2 patients (2.4%), respectively, in nonadherent patients (P < .001 for all parameters). Nonadherence to imatinib treatment and duration of hydroxyurea treatment of more than 12 months before starting imatinib were found to adversely affect PFS in univariate (hazard ratio [HR], 7.5 and 9.7, respectively and P < .001 for both) and multivariate (HR, 5.6 and 9.3; P = .001 and P < .001, respectively) analysis. High risk Sokal score was found to adversely affect PFS in univariate analysis (HR of high to low risk, 2.8; P < .022) but not in multivariate analysis. Yemeni patients who were adherent to imatinib therapy achieved response rates similar to that of international standards. Nonadherence to imatinib treatment and previous duration of hydroxyurea treatment for more than 12 months, as a proxy of long interval between diagnosis and starting imatinib treatment, reduced the optimal response to imatinib therapy.

Sections du résumé

BACKGROUND
In a developing country like Yemen, data are limited regarding the outcome of imatinib treatment of chronic myeloid leukemia and the effect of nonadherence to imatinib treatment and previous duration of hydroxyurea treatment.
PATIENTS AND METHODS
A longitudinal cohort study, which included 164 Yemeni patients, was performed. Data regarding the disease characteristics, adherence to treatment (the medication possession ratio) and outcome were analyzed.
RESULTS
After a median follow-up of 60 months and a median duration of imatinib treatment of 46 months, 79 (48.2%) patients were adherent to treatment. In adherent patients, the overall survival and progression-free survival (PFS) were 78 (98.7%) and 73 patients (92.4%), respectively and major molecular response (MMR) rates at 12 months and at 46 months were 32 (41.0%) and 45 patients (57.0%), respectively, compared with 67 (78.8%), 51 (60%), 5 (6.9%), and 2 patients (2.4%), respectively, in nonadherent patients (P < .001 for all parameters). Nonadherence to imatinib treatment and duration of hydroxyurea treatment of more than 12 months before starting imatinib were found to adversely affect PFS in univariate (hazard ratio [HR], 7.5 and 9.7, respectively and P < .001 for both) and multivariate (HR, 5.6 and 9.3; P = .001 and P < .001, respectively) analysis. High risk Sokal score was found to adversely affect PFS in univariate analysis (HR of high to low risk, 2.8; P < .022) but not in multivariate analysis.
CONCLUSION
Yemeni patients who were adherent to imatinib therapy achieved response rates similar to that of international standards. Nonadherence to imatinib treatment and previous duration of hydroxyurea treatment for more than 12 months, as a proxy of long interval between diagnosis and starting imatinib treatment, reduced the optimal response to imatinib therapy.

Identifiants

pubmed: 31983635
pii: S2152-2650(19)32166-4
doi: 10.1016/j.clml.2019.11.015
pii:
doi:

Substances chimiques

Imatinib Mesylate 8A1O1M485B
Hydroxyurea X6Q56QN5QC

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e144-e153

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Jameel Al-Ghazaly (J)

Department of Medicine, Faculty of Medicine and Health Sciences, Sana'a University, Sana'a, Yemen; Hematology unit, Al-Jomhori Teaching Hospital, Sana'a, Yemen. Electronic address: jameel_alghazaly@yahoo.com.

Waled Al-Dubai (W)

Department of Biochemistry and Cytogenetics, Faculty of Medicine and Health Sciences, Sana'a University, Sana'a, Yemen.

Yousr Noaman (Y)

Molecular Unit, National Oncology Center, Sana'a, Yemen.

Munasser Abdullah (M)

Al-Amana Specialized Laboratories, Sana'a, Yemen.

Leila Al-Gharasi (L)

Hematology unit, Al-Jomhori Teaching Hospital, Sana'a, Yemen.

Gianantonio Rosti (G)

Institute of Hematology and Medical Oncology "Seràgnoli," University of Bologna, Bologna, Italy.

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Classifications MeSH