作者
Giuseppe Saglio, Dong-Wook Kim, Surapol Issaragrisil, Philipp Le Coutre, Gabriel Etienne, Clarisse Lobo, Ricardo Pasquini, Richard E Clark, Andreas Hochhaus, Timothy P Hughes, Neil Gallagher, Albert Hoenekopp, Mei Dong, Ariful Haque, Richard A Larson, Hagop M Kantarjian
发表日期
2010/6/17
期刊
New England Journal of Medicine
卷号
362
期号
24
页码范围
2251-2259
出版商
Massachusetts Medical Society
简介
Background
Nilotinib has been shown to be a more potent inhibitor of BCR-ABL than imatinib. We evaluated the efficacy and safety of nilotinib, as compared with imatinib, in patients with newly diagnosed Philadelphia chromosome–positive chronic myeloid leukemia (CML) in the chronic phase.
Methods
In this phase 3, randomized, open-label, multicenter study, we assigned 846 patients with chronic-phase Philadelphia chromosome–positive CML in a 1:1:1 ratio to receive nilotinib (at a dose of either 300 mg or 400 mg twice daily) or imatinib (at a dose of 400 mg once daily). The primary end point was the rate of major molecular response at 12 months.
Results
At 12 months, the rates of major molecular response for nilotinib (44% for the 300-mg dose and 43% for the 400-mg dose) were nearly twice that for imatinib (22%) (P<0.001 for both comparisons). The rates of complete cytogenetic response by 12 months …
引用总数
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学术搜索中的文章
G Saglio, DW Kim, S Issaragrisil, P Le Coutre… - New England Journal of Medicine, 2010