Department of Psychology, University of Calgary, Calgary, AB, Canada.
Department of Oncology, Division of Psychosocial Oncology, Cumming School of Medicine, University of Calgary, 2202 2 St SW, Calgary, AB, T2S 3C3, Canada.
Support Care Cancer. 2024 Aug 14;32(9):588. doi: 10.1007/s00520-024-08795-7.
In contrast to the extensive literature on fear of cancer recurrence (FCR) experienced by adults, literature evaluating pediatric FCR has just begun to emerge. Given the rapidly expanding body of work assessing FCR in childhood and adolescence, a scoping review was conducted to synthesize existing findings. We aimed to assess (1) the characteristics and methods of this literature, (2) how pediatric FCR has been measured, and (3) the extant knowledge of FCR experienced by pediatric survivors of cancer.
Inclusion criteria were: (1) original reports, (2) participants diagnosed with cancer before age 18, (3) current mean age under 18, (4) FCR was explicitly measured (quantitatively) or captured (qualitatively) via survivor self-report, and (6) published in English. Exclusion criteria were: (1) case studies, and (2) grey literature. Three databases (Embase, MEDLINE, PsycINFO) and reference lists from included studies were searched. All studies were screened for inclusion by two authors and all data were extracted by a single author.
Of 3906 identified studies, 19 were included. Studies (published 1991 - 2023) encompassed diverse geographical locations, study designs, and measurement methods. Few assessed FCR as a primary aim (n = 6, 32%). FCR was experienced by 43 - 90% of pediatric survivors. FCR was often positively associated with somatic symptoms and negatively associated with quality of life and emotional functioning.
FCR is a prevalent issue for children and adolescents. Additional evidence is needed to explore and confirm preliminary findings. Future pediatric FCR studies should aim to align with published priority research areas.
与成人经历的广泛癌症复发恐惧(FCR)文献相比,评估儿科 FCR 的文献才刚刚开始出现。鉴于评估儿童和青少年 FCR 的工作迅速扩展,进行了范围审查以综合现有研究结果。我们旨在评估:(1)该文献的特点和方法;(2)儿科 FCR 是如何测量的;(3)癌症患儿经历 FCR 的现有知识。
纳入标准为:(1)原始报告;(2)18 岁前诊断为癌症的参与者;(3)当前平均年龄低于 18 岁;(4)FCR 通过幸存者自我报告明确测量(定量)或捕获(定性);(6)以英文发表。排除标准为:(1)病例研究;(2)灰色文献。检索了三个数据库(Embase、MEDLINE、PsycINFO)和纳入研究的参考文献列表。两名作者对所有研究进行了纳入筛选,一名作者提取了所有数据。
在 3906 项已确定的研究中,有 19 项被纳入。这些研究(发表于 1991 年至 2023 年)涵盖了不同的地理位置、研究设计和测量方法。很少有研究将 FCR 作为主要目标进行评估(n=6,32%)。43%至 90%的儿科幸存者经历了 FCR。FCR 通常与躯体症状呈正相关,与生活质量和情绪功能呈负相关。
FCR 是儿童和青少年的一个普遍问题。需要更多证据来探索和确认初步发现。未来的儿科 FCR 研究应旨在与已发表的优先研究领域保持一致。