Skip to main navigation Skip to search Skip to main content

Venetoclax-based combinations in AML and high-risk MDS prior to and following allogeneic hematopoietic cell transplant

  • Jan Philipp Bewersdorf
  • , Andriy Derkach
  • , Lohith Gowda
  • , Kamal Menghrajani
  • , Susan DeWolf
  • , Josel D. Ruiz
  • , Doris M. Ponce
  • , Brian C. Shaffer
  • , Roni Tamari
  • , James W. Young
  • , Ann A. Jakubowski
  • , Boglarka Gyurkocza
  • , Alexander Chan
  • , Wenbin Xiao
  • , Jacob Glass
  • , Amber C. King
  • , Sheng F. Cai
  • , Anthony Daniyan
  • , Christopher Famulare
  • , Bernadette M. Cuello
  • Nikolai A. Podoltsev, Mikhail Roshal, Sergio Giralt, Miguel Angel Perales, Stuart Seropian, Christina Cho, Amer M. Zeidan, Thomas Prebet, Eytan M. Stein, Martin S. Tallman, Aaron D. Goldberg, Maximilian Stahl
  • Yale University
  • Memorial Sloan-Kettering Cancer Center
  • Cornell University
  • Rockefeller University

Research output: Contribution to journal › Article › peer-review

30 Scopus citations

Abstract

The role of allogeneic hematopoietic cell transplant (allo-HCT) as consolidation after initial venetoclax therapy and the efficacy of venetoclax salvage therapy for relapse after allo-HCT in patients with acute myeloid leukemia (AML) are unclear. We conducted a retrospective study of patients with AML or myelodysplastic syndrome (MDS) who received venetoclax either before or after allo-HCT at Memorial Sloan Kettering Cancer Center and Yale University from 11 August 2016 to 16 November 2020. Among 39 heavily pretreated patients who received venetoclax before allo-HCT, median OS from allo-HCT was not reached after a median follow up of 12.5 months resulting in a 12-month OS estimate of 79.0%. In 37 patients who had received venetoclax-based combinations as salvage therapy after allo-HCT, the overall response rate was 32% with a median OS of 4.7 months (12-month OS estimate: 43.4%). Four patients underwent a second allo-HCT following venetoclax-based salvage therapy suggesting it as a potential salvage treatment option.

Original languageEnglish
Pages (from-to)3394-3401
Number of pages8
JournalLeukemia and Lymphoma
Volume62
Issue number14
DOIs
StatePublished - 2021

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Acute myeloid leukemia
  • AML
  • MDS
  • transplant
  • venetoclax

Fingerprint

Dive into the research topics of 'Venetoclax-based combinations in AML and high-risk MDS prior to and following allogeneic hematopoietic cell transplant'. Together they form a unique fingerprint.

Cite this