First-line treatment for chronic myeloid leukemia: dasatinib, nilotinib, or imatinib

<p>Abstract</p> <p>Imatinib, a tyrosine kinase inhibitor (TKI) of BCR-ABL, was the standard first-line therapy for chronic myeloid leukemia (CML) for almost 10 years. Dasatinib and nilotinib, two newer drugs with higher potency than imatinib against BCR-ABL and activity against mos...

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Main Authors: Rafiyath Shamudheen, Wei Guoqing, Liu Delong
Format: Article
Language:English
Published: BMC 2010-11-01
Series:Journal of Hematology & Oncology
Online Access:http://www.jhoonline.org/content/3/1/47
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spelling doaj-523084ef9f6046d98918aa1415a08aa32020-11-24T20:56:04ZengBMCJournal of Hematology & Oncology1756-87222010-11-01314710.1186/1756-8722-3-47First-line treatment for chronic myeloid leukemia: dasatinib, nilotinib, or imatinibRafiyath ShamudheenWei GuoqingLiu Delong<p>Abstract</p> <p>Imatinib, a tyrosine kinase inhibitor (TKI) of BCR-ABL, was the standard first-line therapy for chronic myeloid leukemia (CML) for almost 10 years. Dasatinib and nilotinib, two newer drugs with higher potency than imatinib against BCR-ABL and activity against most imatinib-resistant BCR-ABL mutations, have each shown superior efficacy compared with imatinib for first-line treatment of chronic-phase CML in randomized phase 3 trials. With 14 months follow-up time, available data suggest no obvious differences in efficacy between dasatinib and nilotinib. Compared with imatinib, dasatinib is associated with higher rates of pleural effusion and thrombocytopenia, but lower rates of edema, gastrointestinal AEs, musculoskeletal AEs, and rash. Nilotinib is associated with higher rates of dermatologic toxicity, headache, and biochemical abnormalities associated with hepatic and pancreatic toxicity compared with imatinib, but lower rates of edema, gastrointestinal AEs, muscle spasm, and neutropenia. Several studies have shown that poor adherence to imatinib detrimentally affects responses and should be considered in patients with a suboptimal response. The different dosing requirements of dasatinib (once daily with or without food) and nilotinib (twice daily with fasting) may be an additional factor in selecting frontline agents. This review compares and contrasts the three FDA approved first line TKI agents.</p> http://www.jhoonline.org/content/3/1/47
collection DOAJ
language English
format Article
sources DOAJ
author Rafiyath Shamudheen
Wei Guoqing
Liu Delong
spellingShingle Rafiyath Shamudheen
Wei Guoqing
Liu Delong
First-line treatment for chronic myeloid leukemia: dasatinib, nilotinib, or imatinib
Journal of Hematology & Oncology
author_facet Rafiyath Shamudheen
Wei Guoqing
Liu Delong
author_sort Rafiyath Shamudheen
title First-line treatment for chronic myeloid leukemia: dasatinib, nilotinib, or imatinib
title_short First-line treatment for chronic myeloid leukemia: dasatinib, nilotinib, or imatinib
title_full First-line treatment for chronic myeloid leukemia: dasatinib, nilotinib, or imatinib
title_fullStr First-line treatment for chronic myeloid leukemia: dasatinib, nilotinib, or imatinib
title_full_unstemmed First-line treatment for chronic myeloid leukemia: dasatinib, nilotinib, or imatinib
title_sort first-line treatment for chronic myeloid leukemia: dasatinib, nilotinib, or imatinib
publisher BMC
series Journal of Hematology & Oncology
issn 1756-8722
publishDate 2010-11-01
description <p>Abstract</p> <p>Imatinib, a tyrosine kinase inhibitor (TKI) of BCR-ABL, was the standard first-line therapy for chronic myeloid leukemia (CML) for almost 10 years. Dasatinib and nilotinib, two newer drugs with higher potency than imatinib against BCR-ABL and activity against most imatinib-resistant BCR-ABL mutations, have each shown superior efficacy compared with imatinib for first-line treatment of chronic-phase CML in randomized phase 3 trials. With 14 months follow-up time, available data suggest no obvious differences in efficacy between dasatinib and nilotinib. Compared with imatinib, dasatinib is associated with higher rates of pleural effusion and thrombocytopenia, but lower rates of edema, gastrointestinal AEs, musculoskeletal AEs, and rash. Nilotinib is associated with higher rates of dermatologic toxicity, headache, and biochemical abnormalities associated with hepatic and pancreatic toxicity compared with imatinib, but lower rates of edema, gastrointestinal AEs, muscle spasm, and neutropenia. Several studies have shown that poor adherence to imatinib detrimentally affects responses and should be considered in patients with a suboptimal response. The different dosing requirements of dasatinib (once daily with or without food) and nilotinib (twice daily with fasting) may be an additional factor in selecting frontline agents. This review compares and contrasts the three FDA approved first line TKI agents.</p>
url http://www.jhoonline.org/content/3/1/47
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