ATRA treatment in the emergency department is associated with reduced early mortality in acute promyelocytic leukemia—a real-world multicenter retrospective cohort analysis
Early hemorrhagic death in acute promyelocytic leukemia (APL) remains a major, preventable cause of mortality. Although guidelines recommend empiric all-trans retinoic acid (ATRA) at first suspicion of APL, real-world initiation varies. We conducted a multicenter retrospective cohort study within the TriNetX U.S. Collaborative Network to evaluate the impact of early ATRA initiation. Adults with laboratory-confirmed APL (PML-RARA) presenting to the emergency department (ED) were categorized by ATRA initiation within 24 h (early) versus after 24 h (delayed). The primary outcome was 30-day mortality; secondary outcomes included major hemorrhage, ICU admission, thrombosis, and sepsis. Among 596 patients, 137 (23%) received early ATRA. After 1:1 propensity score matching (<i>n</i> = 137 per group), early ATRA was associated with lower 30-day mortality (10.2% <i>vs</i> 26.2%) and reduced major hemorrhage, while other outcomes did not differ. The absolute mortality risk reduction was 16%, yielding a number-needed-to-treat of seven. Early ED ATRA initiation substantially improved survival in PML-RARA-confirmed APL.
Authors
- Joseph O’Brien (ORCID: https://orcid.org/0009-0006-9905-7139)
- Timothy O’Brien (ORCID: https://orcid.org/0000-0001-9028-5481)
- Joseph E. Brown (ORCID: https://orcid.org/0000-0002-9636-9480)
- Ben K. Tomlinson
- Mayher Patel
- Koen van Besien
Institutions
- University of Colorado Boulder (US)
- University Hospitals of Cleveland (US)
- Denver Health Medical Center (US)
- University of Colorado System (US)
- University Hospitals Cleveland Medical Center (US)
- University of Colorado Denver (US)
Publication Details
- Journal
- Leukemia & lymphoma/Leukemia and lymphoma
- Published
- 2026-02-03
- DOI
- https://doi.org/10.1080/10428194.2026.2623196
- Primary Topic
- Retinoids in leukemia and cellular processes
- Type
- article
- Field-Weighted Citation Impact
- 0.00