Utilization of allogeneic hematopoietic stem cell transplantation among patients with newly diagnosed acute myeloid leukemia in California: a population-based linked dataset study
Acute myeloid leukemia (AML) often requires allogeneic hematopoietic cell transplantation (alloHCT) for cure, but historically alloHCT has been strikingly underutilized. Reasons for this remain uncertain at the population level. We examined alloHCT utilization over time and explored associations between demographic / healthcare factors and use of alloHCT by age group (adolescent / young adult [AYA] 15-39 years, adult 40-64 years, older adult 65-79 years) using a linked dataset merging the Center for Internatonal Blood and Marrow Transplant Research, the California Cancer Registry, and the California Patient Discharge Database. Eligibility included patients newly diagnosed with AML in California between 2001-2016 who received induction therapy and had no prior HCT. Multivariable Fine-Gray regression analyses were fitted separately across age groups. Among 7,925 patients with AML, alloHCT utilization increased over time across all age groups; however, in the most recent time period studied (2011-2016), utilization within two years of diagnosis remained lowest in older adults (13%) relative to adults (41%) and AYA (49%). Factors statistically significantly associated with lower alloHCT utilization were: 1) AYA: female sex, lower neighborhood socioeconomic status (nSES), uninsured or Indian Health Services (IHS) coverage; 2) adults: older age, male sex, non-Hispanic Black or Asian race and ethnicity, unmarried, lower nSES, uninsured or covered by Medicaid, Medicare, or IHS, higher comorbidity, and living 100+ miles from a transplant center; and 3) older adults: older age, Asian race, and unmarried. In conclusion, using a population-based linked dataset, we demonstrate that utilization of alloHCT among older patients newly diagnosed with AML remains low in California, and factors associated with utilization vary by age group.
Authors
- Lindsay McOmber Morton (ORCID: https://orcid.org/0000-0001-9767-2310)
- Lori S. Muffly (ORCID: https://orcid.org/0000-0002-9887-6136)
- Renata Abrahão (ORCID: https://orcid.org/0000-0002-1644-0313)
- Rafeek A. Yusuf (ORCID: https://orcid.org/0000-0003-3669-0210)
- Ted Wun (ORCID: https://orcid.org/0000-0003-1117-6450)
- Sara J. Schonfeld (ORCID: https://orcid.org/0000-0002-4368-4647)
- Bryan Valcárcel (ORCID: https://orcid.org/0000-0003-3853-2603)
- Ann Brunson (ORCID: https://orcid.org/0000-0001-5308-9457)
- Christa L. Meyer (ORCID: https://orcid.org/0000-0003-2660-2344)
- Jeffery J. Auletta (ORCID: https://orcid.org/0000-0002-1515-2141)
- Theresa H.M. Keegan (ORCID: https://orcid.org/0000-0002-1961-4008)
Institutions
- National Institutes of Health (US)
- Nationwide Children's Hospital (US)
- National Marrow Donor Program (US)
- Stanford Blood Center (US)
- National Cancer Institute (US)
- UC Davis Comprehensive Cancer Center
- University of California, Davis (US)
- Stanford University (US)
Publication Details
- Journal
- Haematologica
- Published
- 2024-08-29
- DOI
- https://doi.org/10.3324/haematol.2024.285648
- Citations
- 1
- Primary Topic
- Acute Myeloid Leukemia Research
- Type
- article
- Field-Weighted Citation Impact
- 0.45
Funders
- Amgen
- Bristol-Myers Squibb
- Pfizer
- Astellas Pharma US
- AstraZeneca
- GlaxoSmithKline
- Sanofi
- California Department of Public Health
- Gilead Sciences
- HistoGenetics
- CSL Behring
- StemCyte
- Actinium Pharmaceuticals
- Vertex Pharmaceuticals
- Jazz Pharmaceuticals
- TG Therapeutics
- Mallinckrodt Pharmaceuticals
- Atara Biotherapeutics
- CareDx
- Adaptive Biotechnologies
- BeiGene
- Incyte
- Omeros Corporation
- Kiadis Pharma
- Astellas Pharma
- Swedish Orphan Biovitrum
- MorphoSys
- Medac
- Centers for Disease Control and Prevention
- Health Resources and Services Administration
- Takeda Oncology
- Kite Pharma
- Pharmacyclics
- Legend Biotech
- Office of Naval Research
- National Cancer Institute
- National Institute of Allergy and Infectious Diseases