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Supplemental Pioglitazone to Patients of CML with Suboptimal TKI Response: A Pragmatic Pilot Study.
Yanamandra, Uday; Yadav, Naveen; Pramanik, Suman; Kapoor, Rajan; Mishra, Kundan; Khurana, Harshit; Sharma, Sanjeevan; Das, Satyaranjan.
Afiliación
  • Yanamandra U; Department of Internal Medicine, Armed Forces Medical College, Pune, 411040 India.
  • Yadav N; Department of Internal Medicine, Armed Forces Medical College, Pune, 411040 India.
  • Pramanik S; Department of Hematology & Stem Cell Transplant, Army Hospital (Research & Referral), Delhi, 110010 India.
  • Kapoor R; Department of Hematology & Stem Cell Transplant, Army Hospital (Research & Referral), Delhi, 110010 India.
  • Mishra K; Department of Hematology & Stem Cell Transplant, Army Hospital (Research & Referral), Delhi, 110010 India.
  • Khurana H; Department of Hematology and Bone Marrow Transplantation, Command Hospital (Southern Command), Pune, 411040 India.
  • Sharma S; Department of Internal Medicine, Command Hospital (Central Command), Lucknow, 226002 India.
  • Das S; Department of Hematology and Bone Marrow Transplantation, Command Hospital (Southern Command), Pune, 411040 India.
Indian J Hematol Blood Transfus ; 39(1): 71-76, 2023 Jan.
Article en En | MEDLINE | ID: mdl-36699425
ABSTRACT
Tyrosine kinase inhibitors (TKIs) have improved outcomes of chronic myeloid leukemia (CML). However, 20-30% of patients require second-line TKIs following suboptimal response. The cost and adverse events limit their use in resource-constraint settings. We conducted a pilot study to ascertain the benefit of adding pioglitazone to TKIs with suboptimal response in real-world resource-constraint settings. In this pragmatic pilot study from 01 Jan 2017 to 31 July 2021, CML patients from a tertiary care center in North India with sub-optimal response to TKIs were additionally given pioglitazone after ruling out imatinib resistance mutation (n - 31). Pioglitazone was stopped if there was disease progression on follow-up, and second-line TKI was started. The data were analyzed with the intention-to-treat principle using JMP Ver.15.1.1. The median age of the study population was 54y (27-82), who were followed up for a median duration of 1023.5d (59-1117). Pioglitazone showed the benefit of one-log reduction in BCR-ABL in 89.7% of the study participants. 1y, 2y and 3y-PFS were 92.57%, 76.5%, and 68.3% respectively. During follow-up period, the disease progressed in 38.7%, of which two succumbed. No adverse events to Pioglitazone were documented. This study proved that adding Pioglitazone to the existing TKI regime in CML with sub-optimal response can benefit. The addition of Pioglitazone was well tolerated. Supplementary Information The online version contains supplementary material available at 10.1007/s12288-022-01561-x.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Indian J Hematol Blood Transfus Año: 2023 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Indian J Hematol Blood Transfus Año: 2023 Tipo del documento: Article