Dordaviprone Maintenance After Allogeneic HCT for High-Risk Acute Myeloid Leukemia and Myelodysplastic Neoplasm.

Am J HematolJun 26, 2026 (epub)
Clinical ResearchHematologyOncology (Medical)Open access

Vijaya Raj Bhatt, Christopher S Wichman, Alyssa Bouska et al.

✦ AI-curated · Sources linked

In 30 seconds

This Phase I clinical trial evaluated the safety of dordaviprone maintenance therapy after allogeneic hematopoietic cell transplantation in 20 adults with high-risk acute myeloid leukemia (AML) or myelodysplastic neoplasm (MDS). The study found no dose-limiting toxicities, and at 2 years, relapse-free survival was 60% and overall survival was 70%.

Key findings

  • No dose-limiting toxicities or graft failures were observed during the trial.
  • Grade ≥3 adverse events occurred in 45% of patients, with 15% deemed related to treatment.
  • At 2 years, relapse-free survival was 60% and overall survival was 70%.

Why it matters

The findings suggest that dordaviprone may be a safe maintenance therapy option for patients with high-risk AML and MDS post-transplant, potentially improving survival outcomes in this vulnerable population.

Source

Published in Am J Hematol. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

ShareTelegramLinkedIn

AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

More in Hematology

Want this personalized?

Stop searching the literature. Choose what you follow and xxcode will build your personalized medical digest.

  • Your specialties
  • Your filters and thresholds
  • Clinical Research + Case Reports, tuned separately
  • Automatic weekly delivery
  • Audio and text

Prefer listening? Personalized audio digests are available with Pro.

Stay updated for free

Get the 3 most interesting publications in one specialty each week.

Weekly email. Unsubscribe anytime.