Evidence map›Paper›PMID 39907876›Full record

Trial reportAnnals of surgical oncology2025

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

Esther N Dekker, Quisette P Janssen, Jacob L van Dam, Gaby J Strijk, Eva M M Verkolf, Sridhar Kandala, Jasper Dumas, Amine Fellah, Eileen M O'Reilly, Marc G Besselink and 7 more

Abstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in Annals of surgical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Esther N DekkerDepartment of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Quisette P JanssenDepartment of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Jacob L van DamDepartment of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Gaby J StrijkDepartment of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Eva M M VerkolfDepartment of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Sridhar KandalaDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Jasper DumasDepartment of Pathology, Tumor Immuno-Pathology Laboratory, Erasmus MC, Rotterdam, The Netherlands.
Amine FellahDepartment of Pathology, Tumor Immuno-Pathology Laboratory, Erasmus MC, Rotterdam, The Netherlands.
Eileen M O'ReillyDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Marc G BesselinkCancer Center Amsterdam, Amsterdam UMC, Amsterdam, The Netherlands.
Casper H J van EijckDepartment of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Marjolein Y V HomsDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Geert-Jan van TienhovenCancer Center Amsterdam, Amsterdam UMC, Amsterdam, The Netherlands.
Johanna W WilminkCancer Center Amsterdam, Amsterdam UMC, Amsterdam, The Netherlands.
Dana A M MustafaDepartment of Pathology, Tumor Immuno-Pathology Laboratory, Erasmus MC, Rotterdam, The Netherlands.
Bas Groot KoerkampDepartment of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands. b.grootkoerkamp@erasmusmc.nl.ORCID http://orcid.org/0000-0003-1917-6973
Dutch Pancreatic Cancer Group

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
KWF Kankerbestrijding 10955NCI NIH HHS P30 CA008748ZonMw 843004108
6 · The paper itself

Abstract

backgroundThis study aimed to investigate the feasibility and yield of blood sample collection in an investigator-initiated nationwide randomized controlled trial (RCT).

methodsIn 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.

resultsOf 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.

conclusionBlood 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.

Indexed as

Biomarkers, TumorBlood Specimen CollectionPancreatic NeoplasmsAgedFeasibility StudiesFemaleFollow-Up StudiesHumansMaleMiddle AgedNeoadjuvant TherapyPrognosisRandomized Controlled Trials as TopicBiomarkers, TumorBiomarkersPancreatic cancerPersonalized medicineRandomized controlled trial

Identifiers

PMID39907876
PMCPMC12130148

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.