作者
Charles L Sawyers, Andreas Hochhaus, Eric Feldman, John M Goldman, Carole B Miller, Oliver G Ottmann, Charles A Schiffer, Moshe Talpaz, Francois Guilhot, Michael WN Deininger, Thomas Fischer, Steve G O'Brien, Richard M Stone, Carlo B Gambacorti-Passerini, Nigel H Russell, Jose J Reiffers, Thomas C Shea, Bernard Chapuis, Steven Coutre, Sante Tura, Enrica Morra, Richard A Larson, Alan Saven, Christian Peschel, Alois Gratwohl, Franco Mandelli, Monique Ben-Am, Insa Gathmann, Renaud Capdeville, Ronald L Paquette, Brian J Druker
发表日期
2002/5/15
期刊
Blood, The Journal of the American Society of Hematology
卷号
99
期号
10
页码范围
3530-3539
出版商
American Society of Hematology
简介
Blast crisis is the most advanced stage of chronic myelogenous leukemia (CML) and is highly refractory to therapy. CML is caused by expression of the chimeric BCR-ABL tyrosine kinase oncogene, the product of the t(9;22) Philadelphia translocation. Imatinib (Glivec, formerly STI571) is a rationally developed, orally administered inhibitor of the Bcr-Abl tyrosine kinase. A total of 260 patients with CML were enrolled in a phase II trial, of whom 229 had a confirmed diagnosis of CML in blast crisis. Patients were treated with imatinib in daily oral doses of 400 mg or 600 mg. Imatinib induced hematologic responses in 52% of patients and sustained hematologic responses lasting at least 4 weeks in 31% of patients, including complete hematologic responses in 8%. For patients with a sustained response, the estimated median response duration was 10 months. Imatinib induced major cytogenetic responses in 16% of …
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