ICON Clinical Research, Lifecycle Sciences Group, 188 Embarcadero, Suite 200, San Francisco, California 94105, USA.
Oncologist. 2010;15(3):308-16. doi: 10.1634/theoncologist.2009-0034. Epub 2010 Feb 26.
Patient-reported outcomes (PROs) are essential for evaluating treatment effects on health-related quality of life and symptoms from the patient's perspective. This study sought to evaluate the psychometric properties of the nine-item Functional Assessment of Cancer Therapy/National Comprehensive Cancer Network Colorectal Cancer Symptom Index (FCSI-9) in a metastatic colorectal cancer (mCRC) population.
The FCSI-9 and EQ-5D were administered every 2-4 weeks to mCRC subjects in a phase III clinical trial. Three hundred ninety-one mCRC subjects completed the questionnaires at baseline and at least one follow-up assessment. Internal consistency reliability, test-retest reliability, construct validity, known groups validity, responsiveness, and the minimum important difference (MID) of the FCSI-9 were evaluated.
The internal consistency and test-retest reliability of the FCSI-9 were acceptable (0.81 and 0.76, respectively). Construct validity was supported based on moderate correlations with the EQ-5D. Known groups validity was evaluated by examining the FCSI-9 scores of subjects categorized by their Eastern Cooperative Oncology Group performance status (PS) score. Subjects with better PS scores reported significantly higher FCSI-9 scores than those with lower PS scores at both baseline and week 8. Responsiveness, as measured by Guyatt's statistic, was 0.77 from baseline to week 8 and 0.60 from week 4 to week 12. Considering all data together, the MID of the FCSI-9 is estimated to be in the range of 1.5-3.0 points.
Results provide preliminary evidence of the reliability, validity, and responsiveness of the FCSI-9.
患者报告的结局(PROs)对于从患者角度评估治疗对健康相关生活质量和症状的影响至关重要。本研究旨在评估九项癌症治疗功能评估/国家综合癌症网络结直肠癌症状指数(FCSI-9)在转移性结直肠癌(mCRC)人群中的心理测量特性。
在一项 III 期临床试验中,每隔 2-4 周向 mCRC 受试者发放 FCSI-9 和 EQ-5D。391 名 mCRC 受试者在基线和至少一次随访评估时完成了问卷。评估了 FCSI-9 的内部一致性信度、重测信度、结构效度、已知组有效性、反应性和最小重要差异(MID)。
FCSI-9 的内部一致性和重测信度可接受(分别为 0.81 和 0.76)。结构效度基于与 EQ-5D 的中度相关性得到支持。通过检查按东部合作肿瘤学组表现状态(PS)评分分类的受试者的 FCSI-9 评分来评估已知组有效性。在基线和第 8 周,PS 评分较好的受试者报告的 FCSI-9 评分明显高于 PS 评分较低的受试者。以盖亚特统计量衡量的反应性,从基线到第 8 周为 0.77,从第 4 周到第 12 周为 0.60。考虑到所有数据,FCSI-9 的 MID 估计在 1.5-3.0 分之间。
结果提供了 FCSI-9 的可靠性、有效性和反应性的初步证据。