PO.PS01.10 · 人群科学

考察癌症幸存者中健康社会决定因素与临床试验参与:一项多州横断面研究

Examining social determinants of health and clinical trial participation among cancer survivors: A multi-state cross-sectional study

海报缩略图:考察癌症幸存者中健康社会决定因素与临床试验参与:一项多州横断面研究
编号 861 展板 7 时间 4/19 02:00–05:00 区域 Section 34 主讲 Amrita Mukunda, BA
分会场 Survivorship Research
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作者与单位 Authors & Affiliations

Amrita S. Mukunda1, Hui Xie2, Priyanka N. Srinivasan1, Qian Wang3

1Case Western Reserve University School of Medicine, Cleveland, OH,2Joseph J. Zilber School of Public Health, University of Wisconsin-Milwaukee, Milwaukee, WI,3Seidman Cancer Center University Hospitals, Cleveland, OH

摘要 Abstract

中文摘要
引言:临床试验对于推进癌症治疗选择以及为患者提供获得新型疗法的机会至关重要,但癌症患者的招募和参与率仍然较低。本研究考察了健康社会决定因素(SDOH)是否与癌症幸存者的临床试验参与相关。 方法:本横断面研究分析了2022年至2024年行为风险因素监测系统数据。样本包括来自15个州和2个美国属地、年龄18岁及以上的癌症幸存者。通过对九个领域的二分类回答求和计算SDOH综合评分(范围0-9):生活满意度、社会/情感支持、孤独/孤立、就业中断、SNAP福利、食物不安全、住房/公用事业付款困难、公用事业服务停供威胁以及交通障碍。综合评分越高表示社会劣势越大。校正后的逻辑回归模型识别了与临床试验参与相关的因素。所有分析均进行了加权。 结果:在6,929例癌症幸存者中,370例(5.34%)报告曾将临床试验参与作为其治疗的一部分。与非参与者相比,将临床试验参与作为治疗一部分的癌症幸存者更年轻、更可能为女性且来自种族/族裔少数群体(所有p值<0.05)。在校正年龄、性别、种族/族裔、婚姻状况、收入、合并症负担和医疗保险类型后,SDOH综合评分与临床试验参与无关。在考察各个SDOH因素时,过去12个月中经历过公用事业服务停供威胁(电、燃气、油和/或水)的癌症幸存者参与临床试验的可能性较低(aOR:0.504,95% CI:0.257-0.989,p=0.046)。此外,与拥有Medicaid的幸存者相比,拥有私人保险的癌症幸存者(aOR:1.62,95% CI:1.14-2.30,p=0.007)和Medicare受益人(aOR:1.69,95% CI:1.22-2.33,p=0.001)参与临床试验的可能性更高。 结论:总体SDOH负担与癌症幸存者的临床试验参与无关;然而,保险类型和反映财务脆弱性的个别决定因素确实产生了显著影响。虽然拥有私人保险的幸存者和Medicare受益人表现出较高的参与率,但经历公用事业停供威胁者的参与率显著降低。这些发现凸显了解决财务压力源对于改善癌症患者临床试验可及性的重要性。
查看英文原文 English abstract
Introduction: Clinical trials are essential for advancing cancer treatment options and providing patients access to novel therapies, yet recruitment and participation among cancer patients remain low. This study examined whether social determinants of health (SDOH) were associated with clinical trial participation among cancer survivors. Methods: This cross-sectional study analyzed Behavioral Risk Factor Surveillance System data from 2022 to 2024. The sample included cancer survivors aged 18 years or older from 15 states and 2 U.S. territories. An SDOH composite score (range 0-9) was calculated by summing binary responses across nine domains: life satisfaction, social/emotional support, loneliness/isolation, employment disruption, SNAP benefits, food insecurity, housing/utility payment difficulty, threats of utility service shut-off, and transportation barriers. A higher composite score indicated greater social disadvantage. Adjusted logistic regression models identified factors associated with clinical trial participation. All analyses were weighted. Results: Of the 6,929 cancer survivors, 370 (5.34%) reported clinical trial participation as part of their treatment. Cancer survivors who participated in a clinical trial as part of their treatment were younger, more likely to be female, and from racial/ethnic minority groups compared to non-participants (all p-values <0.05). After adjusting for age, sex, race/ethnicity, marital status, income, comorbidity burden, and health insurance type, SDOH composite score was not associated with clinical trial participation.When examining individual SDOH factors, cancer survivors who had experienced threats of utility service shut-offs (electric, gas, oil, and/or water) in the past 12 months were less likely to have participated in clinical trials (aOR: 0.504, 95% CI: 0.257-0.989, p=0.046). Additionally, cancer survivors with private insurance (aOR: 1.62, 95% CI: 1.14-2.30, p=0.007) and Medicare beneficiaries (aOR: 1.69, 95% CI: 1.22-2.33, p=0.001) were more likely to participate in clinical trials compared to those with Medicaid. Conclusion: Overall SDOH burden was not associated with clinical trial participation among cancer survivors; however, insurance type and individual determinants of financial vulnerability did have a significant impact. While privately insured survivors and Medicare beneficiaries showed higher participation, those experiencing utility shut-off threats had significantly reduced participation. These findings highlight the importance of addressing financial stressors to improve clinical trial access for patients with cancer.
利益披露 Disclosure
A. S. Mukunda, None.. H. Xie, None.. P. N. Srinivasan, None.. Q. Wang, None.

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