肺癌免疫治疗患者报告结局量表的编制及信效度检验

    Development and Validation of a Patient-Reported Outcome Measure for Lung Cancer Patients Undergoing Immunotherapy

    • 摘要:
      目的 编制肺癌免疫治疗患者报告结局量表并检验其信效度,以期为患者报告结局提供有效的自我评估工具。
      方法 2025年2月—8月,通过文献分析、病例回顾、半结构访谈及小组讨论形成量表条目池;通过专家函询确定初始版量表;2025年10月—2026年2月,采用便利抽样法,选取广东省某三级甲等医院的肺癌免疫治疗患者进行调查,筛选量表条目并进行信效度检验。
      结果 肺癌免疫治疗患者报告结局量表共4个领域,17个维度,57个条目,探索性因子分析在4个领域分别提取9、2、3、3个公因子,累计方差贡献率分别为73.984%、79.044%、78.637%、79.735%,量表总体分半信度系数为0.765,总体Cronbach’ s α为0.914,重测信度为0.908,内部一致性信度好,量表内容效度指数为0.906。
      结论 构建的肺癌免疫治疗患者报告结局量表信效度良好,可用于评估肺癌免疫检查点抑制剂治疗患者的自我报告结局。

       

      Abstract:
      Objective To develop a patient-reported outcome measure for lung cancer patients undergoing immunotherapy and to test its reliability and validity, to provide an effective self-assessment tool for patient-reported outcomes.
      Methods From February to August 2025, an item pool was constructed through literature analysis, case review, semi-structured interviews, and group discussions. The preliminary version of the measure was established via expert consultation. From October 2025 to February 2026, a convenience sample of lung cancer patients receiving immunotherapy was recruited from a tertiary hospital in Guangdong Province to refine the measure items and assess its reliability and validity.
      Results The final patient-reported outcome measure for lung cancer patients undergoing immunotherapy consisted of 4 domains, 17 dimensions, and 57 items. Exploratory factor analysis extracted 9, 2, 3, and 3 common factors in the four domains, with cumulative variance contributions of 73.984%, 79.044%, 78.637%, and 79.735%, respectively. The overall split-half reliability coefficient was 0.765, the overall Cronbach’s α was 0.914, and the test-retest reliability was 0.908, indicating good internal consistency. The scale-level content validity index was 0.906.
      Conclusion The patient-reported outcome measure developed for lung cancer patients receiving immune checkpoint inhibitor therapy demonstrates good reliability and validity and can be used to assess patient-reported outcomes in this population.

       

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