Veldhuijzen Evalien, Walraven Iris, Belderbos José
Department of Radiation Oncology, Netherlands Cancer Institute, Amsterdam, Netherlands.
Department for Health Evidence, Radboud University Medical Center, Nijmegen, Netherlands.
JMIR Cancer. 2021 Sep 14;7(3):e26574. doi: 10.2196/26574.
The Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) item library covers a wide range of symptoms relevant to oncology care. There is a need to select a subset of items relevant to specific patient populations to enable the implementation of PRO-CTCAE-based symptom monitoring in clinical practice.
The aim of this study is to develop a PRO-CTCAE-based subset relevant to patients with lung cancer that can be used for monitoring during multidisciplinary clinical practice.
The PRO-CTCAE-based subset for patients with lung cancer was generated using a mixed methods approach based on the European Organization for Research and Treatment of Cancer guidelines for developing questionnaires, comprising a literature review and semistructured interviews with both patients with lung cancer and health care practitioners (HCPs). Both patients and HCPs were queried on the relevance and impact of all PRO-CTCAE items. The results were summarized, and after a final round of expert review, a selection of clinically relevant items for patients with lung cancer was made.
A heterogeneous group of patients with lung cancer (n=25) from different treatment modalities and HCPs (n=22) participated in the study. A final list of eight relevant PRO-CTCAE items was created: decreased appetite, cough, shortness of breath, fatigue, constipation, nausea, sadness, and pain (general).
On the basis of the literature and both professional and patient input, a subset of PRO-CTCAE items has been identified for use in patients with lung cancer in clinical practice. Future work is needed to confirm the validity and effectiveness of this PRO-CTCAE-based lung cancer subset internationally and in real-world clinical practice settings.
患者报告的不良事件通用术语标准(PRO-CTCAE)项目库涵盖了与肿瘤护理相关的广泛症状。有必要选择与特定患者群体相关的项目子集,以便在临床实践中实施基于PRO-CTCAE的症状监测。
本研究的目的是开发一个与肺癌患者相关的基于PRO-CTCAE的子集,可用于多学科临床实践中的监测。
基于欧洲癌症研究与治疗组织制定问卷的指南,采用混合方法生成肺癌患者的基于PRO-CTCAE的子集,包括文献综述以及对肺癌患者和医疗保健从业者(HCP)的半结构化访谈。询问患者和HCP关于所有PRO-CTCAE项目的相关性和影响。总结结果,经过最后一轮专家评审后,选择了肺癌患者临床相关的项目。
来自不同治疗方式的一组异质性肺癌患者(n=25)和HCP(n=22)参与了研究。创建了一份包含八个相关PRO-CTCAE项目的最终清单:食欲减退、咳嗽、气短、疲劳、便秘、恶心、悲伤和疼痛(全身)。
基于文献以及专业人员和患者的意见,已确定了PRO-CTCAE项目的一个子集,用于肺癌患者的临床实践。未来需要开展工作,在国际上以及实际临床实践环境中确认这个基于PRO-CTCAE的肺癌子集的有效性和实用性。