Venetoclax plus LDAC for newly diagnosed AML ineligible for intensive chemotherapy: a phase 3 randomized placebo-controlled trial
The Alfred Hospital · Monash University · +25 more institutions
Abstract
Effective treatment options are limited for patients with acute myeloid leukemia (AML) who cannot tolerate intensive chemotherapy. Adults age ≥18 years with newly diagnosed AML ineligible for intensive chemotherapy were enrolled in this international phase 3 randomized double-blind placebo-controlled trial. Patients (N = 211) were randomized 2:1 to venetoclax (n = 143) or placebo (n = 68) in 28-day cycles, plus low-dose cytarabine (LDAC) on days 1 to 10. Primary end point was overall survival (OS); secondary end points included response rate, transfusion independence, and event-free survival. Median age was 76 years (range, 36-93 years), 38% had secondary AML, and 20% had received prior hypomethylating agent…
Citation impact
- FWCI
- 60.04
- Percentile
- 100%
- References
- 29
Authors
24- AHAndrew H. WeiCorresponding
The Alfred Hospital, Monash University
- PMPau Montesinos
Hospital Universitari i Politècnic La Fe, Centro de Investigación Biomédica en Red de Cáncer
- VIVladimir Ivanov
Federal Almazov North-West Medical Research Centre
- CDCourtney D. DiNardo
The University of Texas MD Anderson Cancer Center
- JNJan Novák
Charles University, University Hospital Kralovske Vinohrady
Topics & keywords
- Venetoclax
- Medicine
- Internal medicine
- Neutropenia
- Febrile neutropenia
- Hazard ratio
- Chemotherapy regimen
- Cytarabine
- Good health and well-being