PO.PR01.02 · 预防研究

Connect癌症预防研究中用于癌症病因学和预防研究的生物标本采集:指导原则、方法与关键指标

Biospecimen collections for cancer etiology and prevention research in the Connect for Cancer Prevention Study: Guiding principles, approach, and key metrics

海报缩略图:Connect癌症预防研究中用于癌症病因学和预防研究的生物标本采集:指导原则、方法与关键指标
编号 5098 展板 12 时间 4/21 09:00–12:00 区域 Section 37 主讲 Nicolas Wentzensen, MD;PhD
分会场 Early Detection and Interception
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作者与单位 Authors & Affiliations

Nicolas A. Wentzensen1, Stephanie J. Weinstein2, Amanda Black3, Erin Schwartz2, Hannah P. Yang4, Michelle Brotzman5, Paul Albert2, Laura E. Beane Freeman2, Amy Berrington de Gonzalez6, Jonas S. Almeida2, Jonine Figueroa2, Montserrat García-Closas7, Nicole Gerlanc2, Gretchen L. Gierach8, Rena Jones9, Peter Kraft5, Autumn Hullings2, Charles E. Matthews10, Habibul Ahsan11, Brisa Aschebrook-Kilfoy12, Chun-Hung Chan13, Robert Greenlee14, Stacey Honda15, Benjamin A. Rybicki16, Blythe Ryerson17, Katherine Sanchez18, Mark A. Schmidt19, Kevin Skyes18, Larissa L. White20, Jeanette Ziegenfuss21, Stephen J. Chanock5, Christian C. Abnet22, Mia M. Gaudet1

1National Cancer Inst. Div. of Cancer Epidemiology & Genetics, Bethesda, MD,2National Cancer Institute, Bethesda, MD,3Staff Scientist, NCI-DCEG, Bethesda, MD,4Div. of Cancer Epidemiology & Genetics, National Cancer Inst., Bethesda, MD,5National Cancer Institute, Rockville, MD,6The Institute of Cancer Research, United Kingdom, London, United Kingdom,7The Institute of Cancer Research, London, United Kingdom,8Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD,9NCI, Bethesda, MD,10Investigator, Nutritional Epidem. Branch, NCI-DCEG, Bethesda, MD,11Professor, Dept. of Health Studies, Univ. of Chicago Cancer Research Ctr., Chicago, IL,12Univ. of Chicago Cancer Research Ctr., Chicago, IL,13Sanford Research, Sioux Falls, SD,14Marshfield Clinic Research Institute, Marshfield, WI,15Kaiser Permanente, Honolulu, HI,16Henry Ford Health System, Detroit, MI,17Kaiser Permanente, Atlanta, GA,18Baylor Scott and White, Dallas, TX,19Kaiser Permanente, Portland, OR,20Kaiser Permanente, Denver, CO,21Health Partners, Minneapolis, MN,22Investigator, Nutritional Epidem. Branch, National Cancer Institute, Rockville, MD

摘要 Abstract

中文摘要
引言 Connect癌症预防研究是一项新的前瞻性队列研究,具有重复暴露评估和长期随访,目标是在美国研究人群中研究癌症发生、多步骤癌变、早期检测和结局。迄今已在10个美国综合医疗保健系统中招募了超过85,000名参与者。生物标本是实现Connect目标的关键组成部分。在前瞻性队列研究中设计生物标本采集需要在大量、重复采集各类生物标本的需求与参与者负担和成本之间取得平衡。方法 生物标本采集方案参考了文献综述、专家咨询以及评估分析前因素对常测生物标志物影响的试点研究。基线生物标本采集包括抽血采集血清、血浆、无细胞DNA采集管,尿液采集以及漱口水样本。生物标本采集在50多个采集地点进行,包括临床采血基础设施和专用研究实验室内。所有生物标本均运送至NCI中央实验室进行处理和长期储存。过程指标包括样本完整性、样本偏差、温度记录和从采集到处理的时间等。计划每三年进行重复的生物标本采集,以研究不同的暴露窗口和个体内的生物标志物变化,其中在50岁及以上参与者中进行更频繁的采集,以追求癌症早期检测目标。结果 截至2025年10月,81,030名入组参与者中的56,445名(70%)捐献了血液和尿液样本,更多采集正在进行中。我们观察到年龄较大人群中的生物标本捐献比例较高,从30-34岁参与者的56%到66-70岁参与者的83%不等。生物标本采集参与度在性别和种族/族裔方面相似。在采集中,60%来自临床站点,40%来自研究实验室。在研究实验室采集的生物标本中,82%在一天内送达NCI,所有生物标本中超过95%在4天内送达。在寄送试剂盒的参与者中,家庭采集漱口水样本的回收率为77%。在采集的422,000个生物标本管中,94%完整且无偏差记录。超过90%的参与者在生物标本采集时或采集后不久提交了一份简短调查。结论 Connect癌症预防队列结合了电子健康记录数据、先进的调查和重复的生物标本采集,以解决有关癌症病因学和预防的关键问题。我们成功地在全美10个招募站点实施了一套稳健而高效的生物标本采集方法。
查看英文原文 English abstract
Introduction The Connect for Cancer Prevention study is a new prospective cohort with repeated exposure assessment and long-term follow-up with the goals to study cancer initiation, multi-step carcinogenesis, early detection, and outcomes in a US study population. Over 85,000 participants have been recruited so far at 10 U.S. integrated healthcare systems. Biospecimens are a critical component to achieve Connect's goals. Designing biospecimen collections in prospective cohort studies needs to balance the desire for large, repeated collections of various biospecimens with participant burden and cost. Methods The biospecimen collection protocol was informed by literature review, expert consultations, and pilot studies evaluating the effect of pre-analytical factors on commonly measured biomarkers. Baseline biospecimen collection includes a blood draw with serum, plasma, cell-free DNA collection tubes, a urine collection, and a mouthwash sample. Biospecimen collection is performed at over 50 collection locations, including within the clinical phlebotomy infrastructure and dedicated research laboratories. All biospecimens are shipped to a NCI central laboratory for processing and long-term storage. Process metrics include sample completeness, sample deviations, temperature logging, and needle-to-processing time, among others. Repeated biospecimen collections to study different exposure windows and biomarker changes within individuals are planned every three years, with more frequent collections among participants age 50 and older to pursue cancer early detection aims. Results As of October 2025, 56,445 participants of 81,030 enrolled (70%) donated blood and urine samples, with additional collections underway. We observed higher proportions of biospecimen donations in older age groups, ranging from 56% among participants age 30-34 to 83% among 66-70 year olds. Biospecimen collection participation was similar by sex and race/ethnicity. Among the collections, 60% were from clinical sites, and 40% from research laboratories. 82% of biospecimens collected at research laboratories were received at NCI within one day, and over 95% of all biospecimens were received within 4 days. The return of home-collected mouthwash samples was 77% among those sent a kit. Among 422,000 biospecimen tubes collected, 94% were complete with no deviations recorded. Over 90% of participants submitted a short survey at the time or shortly after biospecimen collection. Conclusions The Connect Cohort for Cancer Prevention combines electronic health record data, state-of-the-art surveys, and repeated biospecimen collections to address critical questions on cancer etiology and prevention. We successfully implemented a robust and efficient biospecimen collection approach at 10 recruitment sites across the U.S.
利益披露 Disclosure
N. A. Wentzensen, None.. M. Brotzman, None.. A. Berrington de Gonzalez, None.. B. Aschebrook-Kilfoy, None.. R. Greenlee, None.. S. Honda, None.. B. A. Rybicki, None.. B. Ryerson, None.. K. Sanchez, None.. M. A. Schmidt, None.. K. Skyes, None.. L. L. White, None.. J. Ziegenfuss, None.. S. J. Chanock, None.

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