A Successful Bridge Therapy Combining Hypomethylating Agents with Venetoclax for Adult Patients with Newly Diagnosed or Relapsed/Refractory Acute Myeloid Leukemia

Author:

Bang Su-Yeon12ORCID,Park Silvia12,Kwag Daehun12,Lee Jong Hyuk12ORCID,Min Gi-June12ORCID,Park Sung-Soo12,Yoon Jae-Ho12ORCID,Lee Sung-Eun12ORCID,Cho Byung-Sik12ORCID,Eom Ki-Seong12,Kim Yoo-Jin12,Lee Seok12,Min Chang-Ki1,Cho Seok-Goo1,Lee Jong Wook1ORCID,Kim Hee-Je12ORCID

Affiliation:

1. Department of Hematology, Catholic Hematology Hospital, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea

2. Leukemia Research Institute, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea

Abstract

Recently, the combination of VEN-HMA has been shown to achieve durable responses in patients with both newly diagnosed (ND) and R/R-AML. We retrospectively evaluated the post-allo-HCT outcomes of 50 patients who received VEN-HMA therapy. In total, 10 were ND and 40 were R/R and, at the time of HCT, the median age was 53 years. In the ND- and R/R-AML groups, the percentage of patients who achieved CR/CRi or MLFS was 90% and 92.5%, respectively. In all, after a median follow-up of 13.7 months, the probabilities of overall survival (OS), relapse-free survival (RFS), cumulative incidence of relapse (CIR), and nonrelapse mortality (NRM) at 1 year were 63.7%, 59.3%, 28.5%, and 12.2%, respectively. In addition, the cumulative incidences of grade II–IV acute graft-versus-host disease (GVHD) and moderate–severe chronic GVHD at 1 year were 28.4% and 37.4%, respectively. In multivariate analysis, the factors associated with a statistically significant impact on OS were VEN-HMA cycle (p = 0.021), ELN risk group (p = 0.041), and the response to VEN-HMA therapy before allo-HCT (p = 0.003). Although 80% of our patients had R/R-AML and 30% underwent a second allo-HCT, our data still suggest that allo-HCT following VEN-HMA therapy is a safe and effective treatment option.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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