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转移性葡萄膜黑色素瘤患者最看重的是什么?一项为未来健康相关生活质量测量提供依据的定性研究。

What matters most to people with metastatic uveal melanoma? A qualitative study to inform future measurement of health-related quality of life.

作者信息

Ng Carrie-Anne, Luckett Tim, Mulhern Brendan, Kee Damien, Lai-Kwon Julia, Joshua Anthony M

机构信息

Centre for Health Economics Research and Evaluation (CHERE), Faculty of Health, University of Technology Sydney.

Improving Palliative, Aged and Chronic Care through Clinical Research and Translation (IMPACCT), Faculty of Health, University of Technology Sydney, NSW.

出版信息

Melanoma Res. 2024 Jun 1;34(3):248-257. doi: 10.1097/CMR.0000000000000961. Epub 2024 Mar 5.

Abstract

Metastatic uveal melanoma (mUM) is a rare cancer with poor prognosis, but novel treatments are emerging. Currently, there are no mUM-specific health-related quality of life (HRQL) questionnaires available for clinical research. We aimed to explore how mUM and its treatment affect HRQL and assess the content validity of existing questionnaires. Participants were patients with mUM and healthcare professionals involved in their care. Qualitative data were collected using semi-structured interviews and focus groups. Data collection and analysis used an integrative approach involving inductive questions/coding to elicit new concepts and deductive questions/coding based on domains of existing HRQL questionnaires. Initial interviews/focus groups focussed on HRQL questionnaires designed for patients with uveal melanoma or liver metastases. As new concepts were elicited, domains and items from other questionnaires were subsequently added. Seventeen patients and 16 clinicians participated. HRQL concerns assessed by uveal melanoma-specific questionnaires were largely resolved by the time of metastasis. The Functional Assessment of Cancer Therapy - Immunotherapy Module (FACT-ICM) adequately captured most immunotherapy-related side effects during initial treatment cycles. However, most patients emphasised emotional impacts over physical ones, focussing on the existential threat posed by disease amidst uncertainty about treatment accessibility and effectiveness. Patients were also concerned with treatment burden, including time commitment, travel, need for hospitalisation, and expenses. The relative importance of HRQL issues varied over time and across treatment modalities, with no single questionnaire being sufficient. Pending further development and psychometric testing, clinical researchers may need to take a modular approach to measuring the HRQL impacts of mUM.

摘要

转移性葡萄膜黑色素瘤(mUM)是一种预后较差的罕见癌症,但新的治疗方法正在不断涌现。目前,尚无专门用于临床研究的mUM特异性健康相关生活质量(HRQL)问卷。我们旨在探讨mUM及其治疗如何影响HRQL,并评估现有问卷的内容效度。参与者为mUM患者及参与其护理的医疗专业人员。通过半结构化访谈和焦点小组收集定性数据。数据收集和分析采用综合方法,包括归纳性问题/编码以引出新概念,以及基于现有HRQL问卷领域的演绎性问题/编码。最初的访谈/焦点小组聚焦于为葡萄膜黑色素瘤或肝转移患者设计的HRQL问卷。随着新概念的引出,随后添加了其他问卷的领域和项目。17名患者和16名临床医生参与了研究。到转移发生时,通过葡萄膜黑色素瘤特异性问卷评估的HRQL问题大多已得到解决。癌症治疗功能评估 - 免疫治疗模块(FACT - ICM)在初始治疗周期中充分捕捉了大多数与免疫治疗相关的副作用。然而,大多数患者强调情感影响甚于身体影响,关注疾病在治疗可及性和有效性不确定的情况下所带来的生存威胁。患者还担心治疗负担,包括时间投入、出行、住院需求和费用。HRQL问题的相对重要性随时间和治疗方式而变化,没有单一问卷足以涵盖所有情况。在进一步开发和进行心理测量测试之前,临床研究人员可能需要采用模块化方法来测量mUM对HRQL 的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b79d/11045555/2ccdfac495ee/mr-34-248-g001.jpg

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