Department of Health Services Research, Peter MacCallum Cancer Centre, 305 Grattan Street, Melbourne, Victoria, 3000, Australia.
University of Melbourne, Melbourne, VIC, Australia.
Support Care Cancer. 2022 Oct;30(10):8217-8229. doi: 10.1007/s00520-022-07228-7. Epub 2022 Jul 9.
This study aimed to determine the healthcare experiences, quality of life, and psychosocial needs of patients with cancer of unknown primary (CUP) early after diagnosis; comparing their experiences to patients with advanced cancer of a known primary (non-CUP control patients) and published general population reference data where available.
This study was a cross-sectional, multi-site study comparing CUP patients (n = 139) compared to non-CUP controls (n = 45). Demographic, clinical information and patient-reported outcome questionnaire data were collected at baseline.
Differences in healthcare experienced were found between CUP and non-CUP controls with CUP patients reporting higher scores for unmet medical communication/information needs compared with non-CUP control patients (p = 0.013) as well as greater uncertainty in illness (p = 0.042). Whilst no differences were found between CUP and non-CUP controls on the EORTC and PROMIS measures, of those that 'received written information about your cancer…' and asked '…how useful was it?' fewer CUP patients reported finding the information useful 40% vs 61%, and more were likely to not have received written information at all 59% vs 32%; (p = 0.002). Additionally, of those that found information about their cancer online, fewer patients with CUP reported finding it useful 32% vs 48% control patients (p = 0.005).
CUP patients have unmet medical communication/information needs and greater uncertainty in illness but do not differ in health-related quality of life domains compared to patients with advanced cancer of a known primary.
本研究旨在确定癌症原发灶不明(CUP)患者在确诊后早期的医疗体验、生活质量和心理社会需求;并将其与晚期已知原发灶癌症(非 CUP 对照患者)以及已发表的一般人群参考数据进行比较。
本研究为一项横断面、多中心研究,比较了 CUP 患者(n=139)与非 CUP 对照患者(n=45)。基线时收集人口统计学、临床信息和患者报告的结果测量问卷数据。
CUP 患者与非 CUP 对照患者在医疗体验方面存在差异,CUP 患者报告的未满足医疗沟通/信息需求评分高于非 CUP 对照患者(p=0.013),疾病不确定性也更高(p=0.042)。尽管在 EORTC 和 PROMIS 测量方面,CUP 与非 CUP 对照患者之间未发现差异,但在“收到有关癌症的书面信息……”和“……它有多有用?”这两个问题上,报告信息有用的 CUP 患者比例为 40%,而非 CUP 对照患者比例为 61%;而报告未收到任何书面信息的 CUP 患者比例为 59%,而非 CUP 对照患者比例为 32%(p=0.002)。此外,在那些从网上获取有关癌症信息的患者中,报告发现信息有用的 CUP 患者比例为 32%,而非 CUP 对照患者比例为 48%(p=0.005)。
与晚期已知原发灶癌症患者相比,CUP 患者存在未满足的医疗沟通/信息需求和更高的疾病不确定性,但在健康相关生活质量方面没有差异。