Time burden and treatment patterns of patients with newly diagnosed acute myeloid leukemia receiving parenteral hypomethylating agents in combination with venetoclax
Parenteral hypomethylating agents (HMAs) combined with venetoclax are a first-line treatment for newly diagnosed acute myeloid leukemia (AML) considered ineligible for intensive chemotherapy. Using a retrospective claims database (Humana Healthcare Research Database; 01/01/2019-12/31/2024), time burden, time at home, treatment patterns and persistence were characterized among adults with newly diagnosed AML treated with HMA + venetoclax, from index (first parenteral HMA claim) through end of follow-up (earliest of death, end of insurance eligibility, or end of data). Patients (n = 737; median follow-up: 8.0 months) spent a mean of 11.9 days per month on healthcare visits, with 65.0% of time spent at home or not receiving cancer care. Median time to discontinuation or death on HMA therapy when considering any HMA cycle and label-conforming cycles (≥16 days of venetoclax supply; ≥4/3 days of azacitidine/decitabine) was 5.2 and 2.8 months, respectively. These findings highlight the substantial time burden associated with HMA combined with venetoclax.
Authors
- Fang Sun (ORCID: https://orcid.org/0000-0002-3089-2244)
- Arthur Voegel
- Maryia Zhdanava (ORCID: https://orcid.org/0000-0002-7995-2578)
- Anabelle Tardif‐Samson (ORCID: https://orcid.org/0009-0009-5118-1909)
- Harold N Keer (ORCID: https://orcid.org/0000-0003-0753-4921)
- Amer Methqal Zeidan (ORCID: https://orcid.org/0000-0001-7017-8160)
- Ruizhi Zhao
- Dominic Pilon (ORCID: https://orcid.org/0000-0003-2380-1495)
- Claire Vanden Eynde
- Dina Christensen
Institutions
- Yale University (US)
- Taiho Oncology (United States) (US)
- Analysis Group (United States) (US)
Publication Details
- Journal
- Leukemia & lymphoma/Leukemia and lymphoma
- Published
- 2026-10-28
- DOI
- https://doi.org/10.1080/10428194.2026.2726604
- Primary Topic
- Acute Myeloid Leukemia Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00