作者
Jorge E. Cortés,D. W. Kim,Javier Pinilla‐Ibarz,Philipp le Coutre,Ronald Paquette,Charles Chuah,Franck E. Nicolini,Jane F. Apperley,H. Jean Khoury,Moshe Talpaz,John F. DiPersio,Daniel J. DeAngelo,Elisabetta Abruzzese,Delphine Réa,Michele Baccarani,Martin C. Müller,Carlo Gambacorti‐Passerini,Siu‐Fun Wong,Stephanie Lustgarten,Victor M. Rivera,Tim Clackson,Christopher D. Turner,Frank G. Haluska,François Guilhot,Michael W. Deininger,Andreas Hochhaus,Timothy P. Hughes,John M. Goldman,Neil P. Shah,Hagop M. Kantarjian
摘要
Ponatinib is a potent oral tyrosine kinase inhibitor of unmutated and mutated BCR-ABL, including BCR-ABL with the tyrosine kinase inhibitor–refractory threonine-to-isoleucine mutation at position 315 (T315I). We conducted a phase 2 trial of ponatinib in patients with chronic myeloid leukemia (CML) or Philadelphia chromosome–positive acute lymphoblastic leukemia (Ph-positive ALL).