Luckett Tim, Ng Carrie-Anne, Lai-Kwon Julia, Kee Damien, Mulhern Brendan, Joshua Anthony M
Improving Palliative, Aged and Chronic Care through Clinical Research and Translation (IMPACCT), Faculty of Health, University of Technology Sydney, Building 10, Jones St, Ultimo, Sydney, New South Wales, NSW, 2007, Australia.
Centre for Health Economics Research and Evaluation (CHERE), Faculty of Health, University of Technology Sydney, Sydney, New South Wales, NSW, 2007, Australia.
BMC Cancer. 2025 May 26;25(1):939. doi: 10.1186/s12885-025-14368-6.
The advent of immunotherapies and targeted treatments has improved survival for some people with metastatic cancer but also increased prognostic uncertainty. To inform clinician-patient communication and supportive care, this study explored uncertainty-related coping among people with metastatic uveal melanoma (mUM) - a disease for which treatments have emerged especially suddenly.
A qualitative approach was taken using semi-structured interviews. Participants with mUM were recruited through consumer organisations internationally. Interviews explored participant perspectives on the impacts of uncertainty and their related coping strategies. Analysis involved inductive coding followed by deductive coding against Mishel's (1988) theoretical framework of uncertainty in illness.
Seventeen people participated, including 10 from Australia. Participants described experiencing uncertainty as disempowering but also leveraged the opportunity it presented for remaining hopeful. Some participants used meta-cognition- alluded to as 'tricking' or 'fooling' themselves - to manage inconsistency between hoping for an exceptional response and accepting that benefits were likely to be modest at best. Most participants were able to maintain everyday normalcy but struggled to discuss their illness and treatment with family and friends. Participants reported heightened anxiety in the lead-up to routine scans and while awaiting results.
Coping with uncertainty in the era of immunotherapy and targeted treatments involves 'hoping for the best while preparing for the worst'. Supportive care is especially needed at the time of scans. Some patients may also benefit from help with talking to their social networks. Head-to-head comparisons are needed of differing psychological interventions.
免疫疗法和靶向治疗的出现提高了一些转移性癌症患者的生存率,但也增加了预后的不确定性。为了指导临床医生与患者的沟通以及支持性护理,本研究探讨了转移性葡萄膜黑色素瘤(mUM)患者中与不确定性相关的应对方式——这是一种治疗方法出现得特别突然的疾病。
采用半结构化访谈的定性方法。通过国际消费者组织招募了mUM患者。访谈探讨了参与者对不确定性影响的看法及其相关应对策略。分析包括归纳编码,然后根据米舍尔(1988年)的疾病不确定性理论框架进行演绎编码。
17人参与,其中10人来自澳大利亚。参与者将经历不确定性描述为使人感到无力,但也利用了它所带来的保持希望的机会。一些参与者使用元认知——被称为“欺骗”或“愚弄”自己——来处理希望获得特殊反应与接受收益可能至多适度之间的不一致。大多数参与者能够维持日常正常生活,但在与家人和朋友讨论自己的病情和治疗时遇到困难。参与者报告在常规扫描前以及等待结果时焦虑加剧。
在免疫疗法和靶向治疗时代应对不确定性需要“抱最好的希望,做最坏的打算”。在扫描时尤其需要支持性护理。一些患者在与社交网络交流方面可能也需要帮助。需要对不同的心理干预措施进行直接比较。