Streefkerk Nina, Tissing Wim J E, van der Heiden-van der Loo Margriet, Lieke Feijen Elizabeth A M, van Dulmen-den Broeder Eline, Loonen Jacqueline J, van der Pal Helena J H, Ronckers Cécile M, van Santen Hanneke M, van den Berg Marleen H, Mulder Renée L, Korevaar Joke C, Kremer Leontine C M
Department Pediatric Oncology, Amsterdam UMC, Emma Children's Hospital, University of Amsterdam, Amsterdam, The Netherlands.
Princess Máxima Center for Pediatric Oncology, Heidelberglaan 25, 3584 CS, Utrecht, The Netherlands.
J Cancer Surviv. 2020 Oct;14(5):666-676. doi: 10.1007/s11764-020-00880-0. Epub 2020 May 3.
Studies investigating self-reported long-term morbidity in childhood cancer survivors (CCS) are using heterogeneous outcome definitions, which compromises comparability and include (un)treated asymptomatic and symptomatic outcomes. We generated a Dutch LATER core set of clinically relevant physical outcomes, based on self-reported data. Clinically relevant outcomes were defined as outcomes associated with clinical symptoms or requiring medical treatment.
First, we generated a draft outcome set based on existing questionnaires embedded in the Childhood Cancer Survivor Study, British Childhood Cancer Survivor Study, and Dutch LATER study. We added specific outcomes reported by survivors in the Dutch LATER questionnaire. Second, we selected a list of clinical relevant outcomes by agreement among a Dutch LATER experts team. Third, we compared the proposed clinically relevant outcomes to the severity grading of the Common Terminology Criteria for Adverse Events (CTCAE).
A core set of 74 self-reported long-term clinically relevant physical morbidity outcomes was established. Comparison to the CTCAE showed that 36% of these clinically relevant outcomes were missing in the CTCAE.
This proposed core outcome set of clinical relevant outcomes for self-reported data will be used to investigate the self-reported morbidity in the Dutch LATER study. Furthermore, this Dutch LATER outcome set can be used as a starting point for international harmonization for long-term outcomes in survivors of childhood cancer.
调查儿童癌症幸存者(CCS)自我报告的长期发病率的研究采用了异质性的结局定义,这损害了可比性,且纳入了(未)治疗的无症状和有症状结局。我们基于自我报告数据生成了一套荷兰LATER临床相关身体结局核心集。临床相关结局被定义为与临床症状相关或需要医学治疗的结局。
首先,我们基于儿童癌症幸存者研究、英国儿童癌症幸存者研究和荷兰LATER研究中现有的问卷生成了一个结局集草案。我们添加了荷兰LATER问卷中幸存者报告的特定结局。其次,我们通过荷兰LATER专家团队的共识选择了一份临床相关结局清单。第三,我们将提议的临床相关结局与不良事件通用术语标准(CTCAE)的严重程度分级进行了比较。
建立了一套包含74项自我报告的长期临床相关身体发病结局的核心集。与CTCAE的比较表明,这些临床相关结局中有36%在CTCAE中缺失。
这个提议的自我报告数据临床相关结局核心集将用于调查荷兰LATER研究中的自我报告发病率。此外,这个荷兰LATER结局集可以作为儿童癌症幸存者长期结局国际协调的起点。