scholarly journals A phase 2 study of belinostat (PXD101) in patients with relapsed or refractory acute myeloid leukemia or patients over the age of 60 with newly diagnosed acute myeloid leukemia: a California Cancer Consortium Study

2014 ◽  
Vol 55 (10) ◽  
pp. 2301-2304 ◽  
Author(s):  
Mark H. Kirschbaum ◽  
Kenneth A. Foon ◽  
Paul Frankel ◽  
Christopher Ruel ◽  
Bernadette Pulone ◽  
...  
2019 ◽  
Vol 3 (4) ◽  
pp. 508-518 ◽  
Author(s):  
Guillermo Garcia-Manero ◽  
Yasmin Abaza ◽  
Koichi Takahashi ◽  
Bruno C. Medeiros ◽  
Martha Arellano ◽  
...  

Abstract Pracinostat, a potent oral pan-histone deacetylase inhibitor with modest single-agent activity in acute myeloid leukemia (AML), has shown synergistic antitumor activity when combined with azacitidine. This single-group, multicenter phase 2 study assessed the safety and efficacy of pracinostat combined with azacitidine in patients who were at least 65 years old with newly diagnosed AML and who were ineligible for standard induction chemotherapy. Patients received pracinostat 60 mg/d, 3 d/wk, for 3 consecutive weeks, plus azacitidine 75 mg/m2 daily for 7 days in a 28-day cycle. Primary endpoints were complete remission (CR), CR with incomplete count recovery (CRi), and morphologic leukemia-free state (MLFS) rates of the combination. Secondary endpoints included safety, progression-free survival (PFS), and overall survival (OS) of the regimen. Fifty patients (33 de novo, 12 secondary, and 5 therapy-related AML) were enrolled. Twenty-six patients (52%) achieved the primary endpoint of CR (42%), CRi (4%), and MLFS (6%). Median OS and PFS were 19.1 months (95% confidence interval [CI], 10-26.5 months) and 12.6 months (95% CI, 10-17.7 months), respectively, with a 1-year OS rate of 62%. Forty-three patients (86%) experienced at least 1 grade 3 or worse treatment-emergent adverse event with the combination, with infections (52%), thrombocytopenia (46%), and febrile neutropenia (44%) reported as the most common toxicities. The 30- and 60-day all-cause mortality rates were 2% and 10%, respectively. DNA sequencing revealed somatic mutations at baseline, and clearance rates correlated with response to treatment. Pracinostat plus azacitidine is a well-tolerated and active regimen in the frontline treatment of older patients with AML unfit for intensive therapy. A larger controlled trial is ongoing. This trial was registered at www.clinicaltrials.gov as #NCT01912274.


Cancer ◽  
2017 ◽  
Vol 123 (22) ◽  
pp. 4430-4439 ◽  
Author(s):  
Elias Jabbour ◽  
Nicholas J. Short ◽  
Farhad Ravandi ◽  
Xuelin Huang ◽  
Lianchun Xiao ◽  
...  

Blood ◽  
2013 ◽  
Vol 121 (23) ◽  
pp. 4655-4662 ◽  
Author(s):  
Farhad Ravandi ◽  
Mona Lisa Alattar ◽  
Michael R. Grunwald ◽  
Michelle A. Rudek ◽  
Trivikram Rajkhowa ◽  
...  

Key Points Azacytidine and sorafenib are effective in patients with relapsed and refractory FLT3-mutated AML.


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