作者
Yasmin Abaza,Hagop M. Kantarjian,Stefan Faderl,Elias Jabbour,Nitin Jain,Deborah A. Thomas,Tapan M. Kadia,Gautam Borthakur,Joseph D. Khoury,Jan A. Burger,William G. Wierda,Susan O’Brien,Marina Konopleva,Alessandra Ferrajoli,Partow Kebriaei,Bouthaina S. Dabaja,Steven M. Kornblau,Yesid Alvarado,Naval Daver,Naveen Pemmaraju,Prithviraj Bose,Philip A. Thompson,Hind Al Azzawi,Mary Ann Kelly,Rebecca Garris,Preetesh Jain,Guillermo García-Manero,Jorgé E. Cortes,Farhad Ravandi
摘要
Nelarabine, a water soluble prodrug of 9-β-D-arabinofuranosylguanine (ara-G), is a T-cell specific purine nucleoside analogue. Given its activity in relapsed and refractory T acute lymphoblastic leukemia (T-ALL) and T lymphoblastic lymphoma (T-LBL), we sought to define its role in the frontline treatment of adult patients. Therefore, we conducted a single arm phase 2 study to determine the safety and efficacy of nelarabine in combination with hyper-CVAD in newly diagnosed patients. For induction/consolidation, patients received eight cycles of hyper-CVAD alternating with high-dose methotrexate and cytarabine plus two cycles of nelarabine given at a dose of 650 mg/m