Pevonedistat, a first-in-class NEDD8-activating enzyme inhibitor, combined with azacitidine in patients with AML

Author:

Swords Ronan T.1ORCID,Coutre Steven2,Maris Michael B.3,Zeidner Joshua F.4ORCID,Foran James M.5,Cruz Jose6ORCID,Erba Harry P.7,Berdeja Jesus G.8,Tam Wayne9ORCID,Vardhanabhuti Saran10ORCID,Pawlikowska-Dobler Iwona10ORCID,Faessel Hélène M.10,Dash Ajeeta B.10ORCID,Sedarati Farhad10ORCID,Dezube Bruce J.10ORCID,Faller Douglas V.10ORCID,Savona Michael R.11ORCID

Affiliation:

1. Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL;

2. Department of Medicine, Stanford University, Stanford, CA;

3. Colorado Blood Cancer Institute, Denver, CO;

4. Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC;

5. Mayo Clinic Cancer Center, Jacksonville, FL;

6. Texas Transplant Institute, San Antonio, TX;

7. UAB Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL;

8. Sarah Cannon Research Institute, Nashville, TN;

9. Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY;

10. Millennium Pharmaceuticals, Inc., Cambridge, MA; and

11. Vanderbilt-Ingram Cancer Center, Vanderbilt University School of Medicine, Nashville, TN

Abstract

Key Points RP2D of PEV 20 mg/m2 in PEV/AZA combo did not alter toxicity profile of AZA; dose-limiting toxicities were transiently elevated AST/ALT. In treatment-naive older AML patients, the intent-to-treat ORR was 50%.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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