Social determinants of health and access to allogeneic hematopoietic cell transplantation for acute myeloid leukemia.

IF 23.1 1区 医学 Q1 HEMATOLOGY Blood Pub Date : 2025-06-19 DOI:10.1182/blood.2024027543
Natalie Wuliji, Salene M W Jones, Ted Gooley, Aaron T Gerds, Bruno C Medeiros, Paul J Shami, John Galvin, Kehinde Adekola, Selina Luger, Maria R Baer, David Rizzieri, Tanya M Wildes, Eunice S Wang, Mikkael A Sekeres, Sudipto Mukherjee, Julie Smith, Mitchell Garrison, Kiarash Kojouri, Jacob Appelbaum, Mary-Elizabeth Percival, Brenda M Sandmaier, Stephanie Lee, Frederick R Appelbaum, Rayne Rouce, Mohamed L Sorror
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Abstract

Abstract: Whether allogeneic hematopoietic cell transplant (allo-HCT) to treat acute myeloid leukemia (AML) is equitably accessible regardless of social determinants of health (SDOH) remains unknown. We examined associations of SDOH with access to allo-HCT and other outcomes. Patients presenting for treatment (n = 692) at 13 AML treatment centers were prospectively recruited to a registered clinical trial (number NCT01929408). Various patient-, AML-, and SDOH-specific variables were collected. Outcomes included mortality without allo-HCT, receipt of allo-HCT, and mortality after allo-HCT. Individual multivariable models (Fine-Gray for the first 2 outcomes, Cox regression for the third) were fit for each SDOH variable, adjusting for relevant patient- and AML-specific variables. Allo-HCT was used to treat 46% of patients. A 10% increase in the proportion with less than a high school education, in households receiving Supplemental Nutrition Assistance Program, receiving Supplemental Security Income, or in poverty led to modeled adjusted hazard ratios (aHRs) of 1.21 (0.99-1.46), 1.13 (0.97-1.31), 1.41 (1.01-1.97), and 1.16 (0.96-1.39) for death without allo-HCT. The aHRs were 0.67 (0.55-0.83), 0.88 (0.76-1.01), 0.71 (0.48-1.05), and 0.91 (0.75-1.09) for lessened receipt of allo-HCT. Among those who received allo-HCT, aHRs for mortality were 1.18 (0.87-1.60), 1.13 (0.92-1.38), 1.21 (0.81-1.82), and 1.04 (0.79-1.36). Results highlight increased mortality without allo-HCT and decreased access to allo-HCT, but lesser magnitude of increased mortality after allo-HCT, among patients from lower resourced areas due to limited education and/or increased poverty. Targeted interventions and policy changes are needed to ensure that marginalized patient populations have equitable chances for AML cure compared with others.

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健康和获得异基因造血细胞移植治疗急性髓系白血病的社会决定因素。
同种异体造血细胞移植(allo-HCT)治疗急性髓性白血病(AML)是否可以公平获得,而不考虑健康的社会决定因素(SDOH)仍然未知。我们研究了SDOH与获得allow - hct和其他结果的关系。在13个AML治疗中心接受治疗的患者(n=692)被前瞻性招募到一项注册临床试验(#NCT01929408)。收集各种患者、AML和SDOH特异性变量。结果包括未接受同种异体造血干细胞移植的死亡率、接受同种异体造血干细胞移植的死亡率和同种异体造血干细胞移植后的死亡率。单独的多变量模型(前两个结果为Fine-Gray,第三个结果为Cox回归)适合每个SDOH变量,调整相关的患者和aml特异性变量。Allo-HCT用于治疗46%的患者。在接受补充营养援助计划、接受补充安全收入或贫困的家庭中,接受高中以下教育的比例增加10%,导致模型调整后的风险比(aHRs)为1.21(0.99-1.46)、1.13(0.97-1.31)、1.41(1.01-1.97)和1.16(0.96-1.39)。接受同种异体hct减少的ahr分别为0.67(0.55-0.83)、0.88(0.76-1.01)、0.71(0.48-1.05)和0.91(0.75-1.09)。在接受同种异体hct的患者中,死亡率的ahr分别为1.18(0.87-1.60)、1.13(0.92-1.38)、1.21(0.81-1.82)和1.04(0.79-1.36)。研究结果强调,在资源匮乏地区,由于教育有限和/或贫困加剧,患者在接受同种免疫疗法治疗后死亡率增加,获得同种免疫疗法治疗的机会减少,但接受同种免疫疗法治疗后死亡率增加幅度较小。需要有针对性的干预措施和政策改革,以确保边缘化患者群体与其他人相比有公平的AML治愈机会。
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来源期刊
Blood
Blood 医学-血液学
CiteScore
23.60
自引率
3.90%
发文量
955
审稿时长
1 months
期刊介绍: Blood, the official journal of the American Society of Hematology, published online and in print, provides an international forum for the publication of original articles describing basic laboratory, translational, and clinical investigations in hematology. Primary research articles will be published under the following scientific categories: Clinical Trials and Observations; Gene Therapy; Hematopoiesis and Stem Cells; Immunobiology and Immunotherapy scope; Myeloid Neoplasia; Lymphoid Neoplasia; Phagocytes, Granulocytes and Myelopoiesis; Platelets and Thrombopoiesis; Red Cells, Iron and Erythropoiesis; Thrombosis and Hemostasis; Transfusion Medicine; Transplantation; and Vascular Biology. Papers can be listed under more than one category as appropriate.
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