Department of Oncology, Wayne State University School of Medicine, Detroit, Michigan, USA.
Karmanos Cancer Institute, Detroit, Michigan, USA.
Cancer Med. 2023 Jan;12(1):684-695. doi: 10.1002/cam4.4855. Epub 2022 Jun 2.
Epidemiological studies of cancer survivors have predominantly focused on non-Hispanic White, elderly patients, despite the observation that African Americans have higher rates of mortality. Therefore, we characterized cancer survivorship in younger African American survivors using the Detroit Research on Cancer Survivors (ROCS) study to assess health behaviors and quality of life.
Five hundred and seventeen patients diagnosed with any cancer between the ages of 20-49 (mean age: 42 years; SD: 6.7 years) completed a survey to identify important clinical, behavioral, and sociodemographic characteristics, measures of health literacy, and experiences of discrimination. Quality of life outcomes were evaluated in patients using FACT-G, FACT-Cog, and PROMIS® Anxiety and Depression scales. Stepwise linear and logistic regression were used to assess the association between quality of life measures and participant characteristics.
The mean FACT-G score was 74.1 (SD: 21.3), while the FACT-Cog was 55.1 (SD: 17.1) (FACT-G range 0-108 with higher scores indicating better function; elderly cancer patient mean: 82.2; FACT-Cog 18-item range 0-72 points with higher scores indicating better perceived cognitive functioning; scores <54 indicating cognitive impairment). In addition, 27.1% and 21.6% of patients had a score indicative of moderate or severe anxiety and depression, respectively. Perceived discrimination and the number of discriminatory events were significantly associated with reductions in three of the four quality of life measures. Health literacy was positively associated with all four health measures, while total comorbidity count was negatively associated with three of the four measures.
Younger adult African American cancer survivors who report experiencing discrimination and suffer from multiple comorbid conditions have poorer mental and overall health. Understanding the unique clinical and socioeconomic stressors that influence this patient population is essential for reducing health disparities and improving long-term survivorship.
尽管观察到非裔美国人的死亡率更高,但癌症幸存者的流行病学研究主要集中在非西班牙裔白人和老年患者身上。因此,我们使用底特律癌症幸存者研究(ROCS)来评估健康行为和生活质量,对年轻的非裔美国癌症幸存者的生存状况进行了描述。
517 名年龄在 20-49 岁(平均年龄:42 岁;标准差:6.7 岁)之间被诊断患有任何类型癌症的患者完成了一项调查,以确定重要的临床、行为和社会人口统计学特征、健康素养衡量标准以及经历的歧视情况。使用 FACT-G、FACT-Cog 和 PROMIS®焦虑和抑郁量表评估患者的生活质量结果。使用逐步线性和逻辑回归来评估生活质量测量与参与者特征之间的关联。
平均 FACT-G 得分为 74.1(标准差:21.3),而 FACT-Cog 得分为 55.1(标准差:17.1)(FACT-G 范围为 0-108,得分越高表示功能越好;老年癌症患者的平均得分:82.2;FACT-Cog 18 项范围为 0-72 分,得分越高表示认知功能越好;得分<54 表示认知障碍)。此外,27.1%和 21.6%的患者分别有中度或重度焦虑和抑郁的评分。感知到的歧视和歧视事件的数量与四项生活质量测量中的三项降低显著相关。健康素养与所有四项健康测量均呈正相关,而总合并症计数与四项测量中的三项呈负相关。
报告经历歧视和患有多种合并症的年轻成年非裔美国癌症幸存者的心理健康和整体健康状况较差。了解影响这一患者群体的独特临床和社会经济压力因素对于减少健康差异和改善长期生存至关重要。