Exploring patient reported quality of life in lung cancer patients: A qualitative study of patient-reported outcome measures.

IF 1.4 4区 医学 Q4 ONCOLOGY
Elena Jensen-Marini, Darshini Ayton, John Zalcberg, Robert G Stirling
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引用次数: 0

Abstract

Objective: Lung cancer is the leading cause of cancer-related death globally and provides a major disease burden likely to substantially impact quality of life (QoL). Patient-reported outcome measures (PROMs) have been identified as effective methods of evaluating patient QoL. Existing lung cancer-specific PROMs however have uncertain utility and minimal patient involvement in their design and development. This qualitative study aimed to evaluate the patient perspective of existing PROMs and to explore their appropriateness for population-based descriptions of lung cancer-related QoL.

Methods: A descriptive qualitative study was conducted consisting of semi-structured interviews with 14 patients recruited from the Victorian Lung Cancer Registry and Alfred Hospital using purposive sampling. Interviews first explored the factors most important to lung cancer patients QoL, and second, patient's perspectives on the appropriateness of existing PROMs. Thematic analysis was used to develop themes, and content analysis was conducted to determine PROM acceptability.

Results: Five novel themes were identified by patients as being important impacts on QoL: Personal attitude toward the disease is important for coping; independence is valued; relationships with family and friends are important; relationships with treating team are meaningful; personal and public awareness of lung cancer is limited. These patient-identified impacts are poorly covered in existing lung cancer-specific PROMs. Patients welcomed and appreciated the opportunity to complete PROMs; however, they identified problems with existing PROMs relevance, tone, and formatting.

Conclusion: Existing lung cancer PROMs poorly reflect the five themes identified in this study as most important to lung cancer patients QoL. This study reaffirms the need to review existing PROMs to ensure utility and construct validity. Future PROM development must engage key patient-generated themes and evolve to reflect the changing management and therapeutic landscape.

Abstract Image

探索肺癌患者的生活质量报告:患者报告结果测量的定性研究。
目的:肺癌是全球癌症相关死亡的主要原因,也是可能严重影响生活质量(QoL)的主要疾病负担。患者报告结果测量法(PROMs)被认为是评估患者生活质量的有效方法。然而,现有的肺癌专用 PROMs 的实用性并不确定,而且患者很少参与其设计和开发。本定性研究旨在从患者角度评估现有的 PROMs,并探讨这些 PROMs 是否适合用于基于人群的肺癌相关 QoL 描述:本研究采用半结构化访谈的方式,对从维多利亚州肺癌登记处和阿尔弗雷德医院(Alfred Hospital)招募的 14 名患者进行了描述性定性研究。访谈首先探讨了对肺癌患者生活质量最重要的因素,其次探讨了患者对现有 PROMs 适宜性的看法。访谈采用主题分析法确定主题,并通过内容分析法确定 PROM 的可接受性:结果:患者确定了五个新的主题,认为它们对 QoL 有重要影响:个人对疾病的态度对应对疾病很重要;独立性受到重视;与家人和朋友的关系很重要;与治疗团队的关系很有意义;个人和公众对肺癌的认识有限。在现有的肺癌专用 PROM 中,这些由患者确定的影响很少涉及。患者对有机会填写 PROM 表示欢迎和赞赏,但他们也指出了现有 PROM 在相关性、语气和格式方面存在的问题:结论:现有的肺癌 PROMs 未能很好地反映本研究中确定的对肺癌患者 QoL 最为重要的五个主题。本研究再次证明,有必要对现有的 PROM 进行审查,以确保其实用性和构建有效性。未来的 PROM 开发必须涉及患者提出的关键主题,并不断发展以反映不断变化的管理和治疗情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.40
自引率
0.00%
发文量
175
审稿时长
6-12 weeks
期刊介绍: Asia–Pacific Journal of Clinical Oncology is a multidisciplinary journal of oncology that aims to be a forum for facilitating collaboration and exchanging information on what is happening in different countries of the Asia–Pacific region in relation to cancer treatment and care. The Journal is ideally positioned to receive publications that deal with diversity in cancer behavior, management and outcome related to ethnic, cultural, economic and other differences between populations. In addition to original articles, the Journal publishes reviews, editorials, letters to the Editor and short communications. Case reports are generally not considered for publication, only exceptional papers in which Editors find extraordinary oncological value may be considered for review. The Journal encourages clinical studies, particularly prospectively designed clinical trials.
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