Department of Oncology, Division of Psychosocial Oncology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Department of Cancer Epidemiology and Prevention Research, Alberta Health Services, Cancer Care Alberta, Calgary, AB, Canada.
Support Care Cancer. 2024 Sep 18;32(10):671. doi: 10.1007/s00520-024-08850-3.
The incidence of thyroid cancer has increased exponentially in recent decades. At the same time, there is a growing concern surrounding the overdiagnosis of indolent thyroid cancer, leading to invasive and potentially unnecessary interventions that can significantly impact young patients' lives. Yet, the experiences of survivors of thyroid cancer have been largely understudied. The purpose of this study was to explore the experiences of survivors of early-onset thyroid cancer.
The qualitative research design of hermeneutic phenomenology guided this study. Participants completed a demographic survey and semi-structured interview that was subsequently transcribed verbatim and analyzed using reflexive thematic analysis.
Thirty-six survivors of thyroid cancer (83% female, median age at diagnosis: 37.1 years, median age at interview: 43.5 years) participated. Participants' experiences were characterized by two themes: (1) reconciling the meaning of the "c" word (cancer) as a dangerous and life-threatening diagnosis with lived experience of thyroid cancer and (2) thyroid cancer leaves patients with lifelong physical and emotional scars.
Survivors of early-onset thyroid cancer experience significant short and late effects on their physical and psychosocial well-being. Survivors shared some of the difficulties of having to reconcile what they were told was a "good cancer" and their previously held beliefs of cancer, including feeling lost in the healthcare system and like they could not access services or be impacted because they had been told they had "good cancer." Increased communication of risks and acknowledgement of the perceptions surrounding cancer is needed to help patients make better informed decisions and feel supported throughout their thyroid cancer journey. Gaps in care pathways, especially adjustments post-treatment, should be filled to help support these survivors.
近年来,甲状腺癌的发病率呈指数级增长。与此同时,人们越来越关注惰性甲状腺癌的过度诊断,这导致了侵入性的、潜在的不必要的干预措施,这些措施会对年轻患者的生活产生重大影响。然而,甲状腺癌幸存者的经历在很大程度上还没有得到充分的研究。本研究旨在探讨早发性甲状腺癌幸存者的经历。
解释学现象学的定性研究设计指导了这项研究。参与者完成了一份人口统计学调查和半结构化访谈,随后将访谈内容逐字转录,并使用反思性主题分析进行分析。
36 名甲状腺癌幸存者(83%为女性,诊断时的中位年龄为 37.1 岁,访谈时的中位年龄为 43.5 岁)参与了研究。参与者的经历有两个主题:(1)将“癌症”这个词的含义(癌症)从危险和危及生命的诊断中调和出来,与甲状腺癌的实际经历相协调;(2)甲状腺癌给患者留下了终身的身体和情感创伤。
早发性甲状腺癌幸存者在身体和社会心理福祉方面经历了显著的短期和长期影响。幸存者分享了一些不得不调和他们被告知是“良性癌症”和他们以前对癌症的信念的困难,包括在医疗保健系统中感到迷失,感觉他们无法获得服务或受到影响,因为他们被告知他们有“良性癌症”。需要增加对风险的沟通,并承认癌症周围的观念,以帮助患者做出更好的知情决策,并在整个甲状腺癌治疗过程中感到支持。应该填补护理途径中的差距,特别是治疗后的调整,以帮助支持这些幸存者。