作者
Brian J Druker, Charles L Sawyers, Hagop Kantarjian, Debra J Resta, Sofia Fernandes Reese, John M Ford, Renaud Capdeville, Moshe Talpaz
发表日期
2001/4/5
期刊
New England Journal of Medicine
卷号
344
期号
14
页码范围
1038-1042
出版商
Massachusetts Medical Society
简介
Background
BCR-ABL, a constitutively activated tyrosine kinase, is the product of the Philadelphia (Ph) chromosome. This enzyme is present in virtually all cases of chronic myeloid leukemia (CML) throughout the course of the disease, and in 20 percent of cases of acute lymphoblastic leukemia (ALL). On the basis of the substantial activity of the inhibitor in patients in the chronic phase, we evaluated STI571 (formerly known as CGP 57148B), a specific inhibitor of the BCR-ABL tyrosine kinase, in patients who had CML in blast crisis and in patients with Ph-chromosome–positive ALL.
Methods
In this dose-escalating pilot study, 58 patients were treated with STI571; 38 patients had myeloid blast crisis and 20 had ALL or lymphoid blast crisis. Treatment was given orally at daily doses ranging from 300 to 1000 mg.
Results
Responses occurred in 21 of 38 patients (55 percent) with a myeloid-blast-crisis phenotype; 4 of …
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