Berkeley Maria, Urman Harold, Lee Janet, Xiao Yi, Ferrell Betty, Reb Anne, Debay Marc, Miller Stuart, Lucero Linda, Hudley Anne Charity, Sun Virginia
Department of Population Sciences, City of Hope, 1500 East Duarte Road, Duarte, CA, 91010, USA.
Vital Research, Los Angeles, CA, USA.
Support Care Cancer. 2025 Aug 2;33(8):745. doi: 10.1007/s00520-025-09774-2.
Lung and colorectal cancer (CRC) survivors experience late and long-term treatment effects and challenges with navigating care. Few evidence-based interventions exist to support survivor needs. This paper describes participant recruitment and pre-randomization baseline characteristics and outcomes from a survivorship self-management intervention trial in lung and CRC.
Baseline outcome measures were collected from survivors, primary care providers (PCP), and oncologists. Enrolled participants were survivors of lung or CRC, were 4-6 months post-treatment completion, age 18 or older, and could read and understand English. Survivor outcome measures included geriatric assessment, quality of life (QOL), communication, knowledge, and self-efficacy. PCP and oncologist outcome measures assessed perceived knowledge, communication, and care coordination regarding survivorship care.
The trial completed accrual over 4 years and enrolled 404 participants across 15 clinical practice sites in Southern California. At baseline, most survivors reported high (mean = 71.11/100) levels of physical functioning and social support but moderate (mean = 53.29/100) levels of social interactions. QOL scores were low for emotional and functional well-being, with survivors of lung cancer reporting lower physical well-being (20.92/28) and total QOL (101.1/136). PCPs and oncologists reported minimal problems with exchanging information or transferring care in a timely manner. Survivors reported challenges with timely care, appointments, and support managing treatment effects.
Baseline characteristics illustrate persistent challenges in survivor QOL and perceived quality of care coordination and communication among survivors, oncologists, and PCPs.
Opportunities for improvements in cancer survivorship care delivery exist and will ultimately support survivors' QOL and outcomes.
肺癌和结直肠癌(CRC)幸存者会经历晚期和长期的治疗影响以及护理过程中的挑战。几乎没有基于证据的干预措施来满足幸存者的需求。本文描述了一项肺癌和结直肠癌幸存者自我管理干预试验中的参与者招募、随机分组前的基线特征及结果。
从幸存者、初级保健提供者(PCP)和肿瘤学家处收集基线结局指标。纳入的参与者为肺癌或结直肠癌幸存者,治疗结束后4 - 6个月,年龄18岁及以上,能阅读和理解英语。幸存者结局指标包括老年评估、生活质量(QOL)、沟通、知识和自我效能感。PCP和肿瘤学家的结局指标评估了关于幸存者护理的感知知识、沟通和护理协调情况。
该试验在4年多的时间里完成了入组,在南加州的15个临床实践地点招募了404名参与者。在基线时,大多数幸存者报告身体功能和社会支持水平较高(平均=71.11/100),但社会互动水平中等(平均=53.29/100)。情绪和功能健康方面的生活质量得分较低,肺癌幸存者报告身体幸福感较低(20.92/28)和总体生活质量较低(101.1/136)。PCP和肿瘤学家报告在及时交换信息或转移护理方面问题极少。幸存者报告在及时获得护理、预约以及管理治疗效果的支持方面存在挑战。
基线特征表明,幸存者的生活质量以及幸存者、肿瘤学家和PCP之间护理协调和沟通的感知质量方面存在持续挑战。
改善癌症幸存者护理服务的机会存在,最终将支持幸存者的生活质量和结局。