Borthakur Gautam, Dombret Herve, Schafhausen Philippe, Brummendorf Tim Henrik, Boissel Nicolas, Jabbour Elias, Mariani Mariangela, Capolongo Laura, Carpinelli Patrizia, Davite Cristina, Kantarjian Hagop, Cortes Jorge E
Department of Leukemia, MD Anderson Cancer Center, Houston, USA.
Hopital Saint Louis, Paris, France.
Haematologica. 2015 Jul;100(7):898-904. doi: 10.3324/haematol.2014.115279. Epub 2015 Apr 17.
Danusertib is a pan-aurora kinase inhibitor with potent activity against Abl kinase including the gatekeeper T315I mutant. A phase 1 dose escalation study of danusertib was conducted in patients with accelerated or blastic phase chronic myeloid leukemia or Philadelphia chromosome-positive acute lymphoblastic leukemia. Two dosing schedules were studied: schedule A, in which danusertib was given by 3-hour intravenous infusion daily for 7 consecutive days (days 1-7) in a 14-day cycle, and schedule B, in which the danusertib was given by 3-hour intravenous infusion daily for 14 consecutive days (days 1-14) in a 21-day cycle. A total of 37 patients were treated, 29 with schedule A and eight with schedule B. The recommended phase 2 dose for schedule A was 180 mg/m(2). Enrollment to schedule B was stopped early because of logistical problems with the frequency of infusions. Febrile neutropenia and mucositis were dose-limiting toxicities in schedule A. Four patients with T315I ABL kinase mutation, all treated with schedule A, responded. Danusertib has an acceptable toxicity profile and is active in patients with Bcr-Abl-associated advanced hematologic malignancies. This study was registered with the European Clinical Trails Data Base (EudraCT number 2007-004070-18).
达努塞替布是一种泛极光激酶抑制剂,对包括守门人T315I突变体在内的Abl激酶具有强大活性。在加速期或急变期慢性髓性白血病或费城染色体阳性急性淋巴细胞白血病患者中开展了达努塞替布的1期剂量递增研究。研究了两种给药方案:方案A,在14天周期内,达努塞替布连续7天(第1 - 7天)每天进行3小时静脉输注;方案B,在21天周期内,达努塞替布连续14天(第1 - 14天)每天进行3小时静脉输注。总共治疗了37例患者,29例采用方案A,8例采用方案B。方案A的推荐2期剂量为180 mg/m²。由于输注频率的后勤问题,方案B的入组提前停止。发热性中性粒细胞减少和粘膜炎是方案A中的剂量限制性毒性。4例T315I ABL激酶突变患者均采用方案A治疗,有反应。达努塞替布具有可接受的毒性特征,对Bcr - Abl相关的晚期血液系统恶性肿瘤患者有活性。本研究已在欧洲临床试验数据库注册(欧盟临床试验编号2007 - 004070 - 18)。