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Blood Sample Collection in Randomized Controlled Trials for Biomarker Discovery and Validation: Experience of the PREOPANC-2 Trial.

Annals of Surgical Oncology(2025)

Erasmus MC Cancer Institute | Erasmus MC | Memorial Sloan Kettering Cancer Center | Cancer Center Amsterdam

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Abstract
BACKGROUND:This study aimed to investigate the feasibility and yield of blood sample collection in an investigator-initiated nationwide randomized controlled trial (RCT). METHODS:In the PREOPANC-2 trial, 375 patients with (borderline) resectable pancreatic cancer were randomly assigned to two neoadjuvant regiments in 19 centers in the Netherlands (2018-2021). Blood sample collection was scheduled at seven time points before, during, and after treatment. The primary outcome was the proportion of successfully collected blood samples at each scheduled time point. RESULTS:Of the 375 randomized patients, 12 were excluded from blood sample collection before any treatment. From the remaining 363 patients, 1513 (87 %) of 1748 blood samples were collected, processed, mailed, and centrally stored. The blood samples were collected before treatment from 347 (96 %) of the 363 patients, after the first neoadjuvant cycle from 322 (94 %) of 343 patients, after neoadjuvant treatment (i.e., before surgery) from 260 (83 %) of 313 patients, and after surgery from 210 (77 %) of 271 patients. During the follow-up visits, blood samples were collected from 147 (82 %) of 179 patients 12 months after randomization and from 83 (77 %) of 108 patients after 24 months. A total of 220 samples (13 %) were missing. The most common causes for missing blood samples were scheduling oversights, unsuccessful blood draw attempts, and mailing failures (151 times, 69 %). Blood sample collection was canceled 69 times (31 %) due to COVID-19. CONCLUSION:Blood sample collection in the PREOPANC-2 trial had a yield of 96 % before treatment and an overall yield of 87 %. Collection of blood samples for biomarker studies is feasible in a nationwide RCT.
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Key words
Biomarkers,Personalized medicine,Randomized controlled trial,Pancreatic cancer
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要点】:本研究探讨了在荷兰全国范围内进行的随机对照试验中,血液样本收集的可行性和收获率,以发现和验证生物标志物。

方法】:在PREOPANC-2试验中,375名患有(临界)可切除胰腺癌的患者被随机分配到两种新辅助治疗方案,并在19个中心进行血液样本收集。

实验】:在治疗前、治疗期间和治疗后的七个时间点收集血液样本,共成功收集1748个中的1513个(87%),使用的数据集为PREOPANC-2试验中的患者血液样本,结果显示收集血液样本用于生物标志物研究在全国范围内随机对照试验中是可行的。