PO.PS01.10 · 人群科学
卵巢癌老年女性功能状态的相关因素
Factors associated with functional status among older women with ovarian cancer
作者与单位 Authors & Affiliations
摘要 Abstract
中文摘要
背景:65岁及以上女性占新发卵巢癌诊断的近一半。该患者群体面临功能状态下降的重大风险,即执行满足基本需求和健康所必需的日常基本活动(如穿衣、洗澡、如厕和进食)的能力下降。对该患者群体而言,维持功能独立性是首要优先事项。然而,影响卵巢癌老年女性功能状态的因素仍知之甚少。本研究旨在识别与这一脆弱人群功能状态相关的人口学和临床因素。
方法:我们利用了最小数据集(MDS)的数据,该数据集为美国养老院居住者提供标准化的功能评估。MDS数据与SEER-Medicare关联,以获取癌症诊断和病史。该队列纳入了6,257名于2000-2019年间在65岁及以上诊断为原发性浸润性上皮性卵巢癌的女性。功能状态采用经过验证的日常生活活动(ADL)量表进行量化,范围为0-28,得分越高表示依赖性越大。拟合线性混合效应模型以识别与诊断后第一年功能状态相关的因素,同时考虑重复测量。变量包括诊断时年龄、Charlson合并症指数、肿瘤分期、组织学类型、种族/族裔以及Medicaid参保情况(作为社会经济状况的替代指标)。
结果:诊断时中位年龄为79岁(四分位距74-84岁),大多数在远处转移期诊断(74%)。年龄较大与较高的ADL评分相关(平均差异[MD]=每增加一岁0.07,95%置信区间[CI] 0.05-0.09,p<0.01)。与较高ADL评分相关的其他因素包括:较高的合并症(MD=Charlson合并症指数每增加一个单位0.41,95% CI 0.33-0.50,p<0.01)、较晚的肿瘤分期(远处转移期 vs. 局限期:MD=1.38,95% CI 0.80-1.95,p<0.01)以及非浆液性组织学类型(非浆液性 vs. 浆液性:MD=0.90,95% CI 0.63-1.18,p<0.01)。非白人女性相较于白人女性也观察到较高的ADL评分(黑人、西班牙裔和亚裔/太平洋岛民的MD分别为1.95、1.45、1.14,均p<0.01),以及Medicaid参保患者相较于未参保患者(MD=0.65,95% CI 0.11-1.18,p=0.02)。
结论:年龄较大、合并症较多、肿瘤分期较晚、非浆液性组织学类型、非白人种族/族裔以及Medicaid参保均与卵巢癌老年女性功能依赖性增加独立相关。这些发现提示功能衰退既有生物学驱动因素也有社会经济驱动因素。需要有针对性的支持性护理来减轻功能衰退,尤其是对于晚期疾病、合并症、少数族裔背景和低社会经济状况的女性。
查看英文原文 English abstract
Background: Women aged 65+ account for nearly half of new ovarian cancer diagnoses. This patient group faces a substantial risk of declining functional status, i.e., the capability to carry out essential daily activities necessary for basic needs and health, such as dressing, bathing, toilet use, and eating. For this patient group, maintaining functional independence is a top priority. However, factors influencing functional status in older women with ovarian cancer remain poorly understood. This study aimed to identify demographic and clinical factors associated with functional status in this vulnerable population.
Methods: We utilized data from the Minimum Data Set (MDS), which provides standardized functional assessments for U.S. nursing home residents. MDS data were linked with SEER-Medicare to capture cancer diagnoses and medical histories. The cohort included 6,257 women with primary invasive epithelial ovarian cancer diagnosed at age 65+ between 2000-2019. Functional status was quantified using a validated Activities of Daily Living (ADL) scale ranging from 0-28, with higher scores indicating greater dependency. A linear mixed-effect model was fit to identify factors associated with functional status during the first year after diagnosis, while accounting for repeated measures. Variables included age at diagnosis, Charlson Comorbidity Index, tumor stage, histotype, race/ethnicity, and Medicaid enrollment (as a proxy for socioeconomic status).
Results: Median age at diagnosis was 79 years (interquartile range 74-84 years) with most diagnosed at distant stage (74%). Older age was associated with higher ADL scores (mean difference [MD]=0.07 per one year increase in age, 95% confidence interval [CI] 0.05-0.09, p<0.01). Other factors associated with higher ADL scores included: higher comorbidity (MD=0.41 per unit increase in Charlson Comorbidity Index, 95% CI 0.33-0.50, p<0.01), later tumor stage (distant vs. localized stages: MD=1.38, 95% CI 0.80-1.95, p<0.01) and non-serous histotype (non-serous vs. serous: MD=0.90, 95% CI 0.63-1.18, p<0.01). Higher ADL scores were also observed for non-White vs. White women (MD=1.95, 1.45, 1.14 for Black, Hispanic, and Asian/Pacific Islander, respectively, all p<0.01) and Medicaid-enrolled patients vs. non-enrolled (MD=0.65, 95% CI 0.11-1.18, p=0.02).
Conclusions: Older age, higher comorbidity, later tumor stage, non-serous histotype, non-White race/ethnicity, and Medicaid enrollment are independently associated with increased functional dependency in older women with ovarian cancer. These findings suggest both biological and socioeconomic drivers of functional decline. Targeted supportive care is needed to mitigate functional decline, particularly for women with advanced disease, comorbidities, minority backgrounds, and low socioeconomic status.
利益披露 Disclosure
M. T. Phung, None..
L. M. Barroilhet, None..
N. Binkley, None..
R. E. Gangnon, None..
J. Sobecki, None..
B. Trabert, None..
A. Trentham-Dietz, None.