Division of Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Department of Genetics and Genome Biology, University of Leicester, UK.
Radiother Oncol. 2019 Sep;138:59-67. doi: 10.1016/j.radonc.2019.04.034. Epub 2019 May 27.
REQUITE aimed to establish a resource for multi-national validation of models and biomarkers that predict risk of late toxicity following radiotherapy. The purpose of this article is to provide summary descriptive data.
An international, prospective cohort study recruited cancer patients in 26 hospitals in eight countries between April 2014 and March 2017. Target recruitment was 5300 patients. Eligible patients had breast, prostate or lung cancer and planned potentially curable radiotherapy. Radiotherapy was prescribed according to local regimens, but centres used standardised data collection forms. Pre-treatment blood samples were collected. Patients were followed for a minimum of 12 (lung) or 24 (breast/prostate) months and summary descriptive statistics were generated.
The study recruited 2069 breast (99% of target), 1808 prostate (86%) and 561 lung (51%) cancer patients. The centralised, accessible database includes: physician- (47,025 forms) and patient- (54,901) reported outcomes; 11,563 breast photos; 17,107 DICOMs and 12,684 DVHs. Imputed genotype data are available for 4223 patients with European ancestry (1948 breast, 1728 prostate, 547 lung). Radiation-induced lymphocyte apoptosis (RILA) assay data are available for 1319 patients. DNA (n = 4409) and PAXgene tubes (n = 3039) are stored in the centralised biobank. Example prevalences of 2-year (1-year for lung) grade ≥2 CTCAE toxicities are 13% atrophy (breast), 3% rectal bleeding (prostate) and 27% dyspnoea (lung).
The comprehensive centralised database and linked biobank is a valuable resource for the radiotherapy community for validating predictive models and biomarkers.
Up to half of cancer patients undergo radiation therapy and irradiation of surrounding healthy tissue is unavoidable. Damage to healthy tissue can affect short- and long-term quality-of-life. Not all patients are equally sensitive to radiation "damage" but it is not possible at the moment to identify those who are. REQUITE was established with the aim of trying to understand more about how we could predict radiation sensitivity. The purpose of this paper is to provide an overview and summary of the data and material available. In the REQUITE study 4400 breast, prostate and lung cancer patients filled out questionnaires and donated blood. A large amount of data was collected in the same way. With all these data and samples a database and biobank were created that showed it is possible to collect this kind of information in a standardised way across countries. In the future, our database and linked biobank will be a resource for research and validation of clinical predictors and models of radiation sensitivity. REQUITE will also enable a better understanding of how many people suffer with radiotherapy toxicity.
REQUITE 旨在建立一个资源库,用于对预测放疗后迟发性毒性风险的模型和生物标志物进行跨国验证。本文的目的是提供总结性描述数据。
这是一项国际性、前瞻性队列研究,于 2014 年 4 月至 2017 年 3 月在 8 个国家的 26 家医院招募癌症患者。目标招募人数为 5300 名患者。符合条件的患者患有乳腺癌、前列腺癌或肺癌,且计划接受潜在可治愈的放疗。放疗按照当地方案进行,但各中心均使用标准化的数据收集表格。在治疗前采集血样。患者的随访时间至少为 12 个月(肺癌)或 24 个月(乳腺癌/前列腺癌),并生成总结性描述性统计数据。
该研究共招募了 2069 名乳腺癌(目标患者的 99%)、1808 名前列腺癌(86%)和 561 名肺癌(51%)患者。集中、可访问的数据库包括:医生(47025 份表格)和患者(54901 份表格)报告的结果;11563 张乳腺照片;17107 个 DICOM 和 12684 个 DVHs。有 4223 名欧洲血统(1948 名乳腺癌、1728 名前列腺癌、547 名肺癌)患者的基因型数据可用于推断。1319 名患者可提供放射诱导的淋巴细胞凋亡(RILA)检测数据。集中的生物银行中存储了 4409 份 DNA(n=4409)和 PAXgene 管(n=3039)。2 年(肺癌为 1 年)时≥2 级 CTCAE 毒性的例数的示例患病率为 13%的萎缩(乳腺癌)、3%的直肠出血(前列腺癌)和 27%的呼吸困难(肺癌)。
集中的综合数据库和关联的生物库是放疗界验证预测模型和生物标志物的宝贵资源。
多达一半的癌症患者接受放疗,周围健康组织的照射是不可避免的。对健康组织的损伤会影响短期和长期的生活质量。并非所有患者对辐射“损伤”的敏感性都相同,但目前还无法确定哪些患者是敏感的。REQUITE 的建立旨在努力了解更多关于我们如何预测辐射敏感性的信息。本文的目的是概述和总结可用的数据和材料。在 REQUITE 研究中,4400 名乳腺癌、前列腺癌和肺癌患者填写了问卷并捐献了血液。还以同样的方式收集了大量数据。通过所有这些数据和样本,创建了一个数据库和生物库,表明可以以标准化的方式在各国之间收集此类信息。在未来,我们的数据库和关联的生物库将成为研究和验证辐射敏感性临床预测因子和模型的资源。REQUITE 还将使我们能够更好地了解有多少人受到放疗毒性的影响。