Evidence map›Paper›PMID 39276915›Full record

ArticleCancer letters2024

A rigorous multi-laboratory study of known PDAC biomarkers identifies increased sensitivity and specificity over CA19-9 alone.

Brian Haab, Lu Qian, Ben Staal, Maneesh Jain, Johannes Fahrmann, Christine Worthington, Denise Prosser, Liudmila Velokokhatnaya, Camden Lopez, Runlong Tang and 10 more

Abstract readMulticenter Study
In one paragraph

Article in Cancer letters, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
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  3. Review
  4. Review
  5. Article
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  8. Article
  9. From detection to ruling out in pancreatic cancer: a new perspective.Translational gastroenterology and hepatology · 2026
    Article
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  11. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors.

Brian HaabVan Andel Institute, 333 Bostwick NE, Grand Rapids, MI, 49503, USA. Electronic address: brian.haab@vai.org.
Lu QianFred Hutchinson Cancer Research Center, 1100 Fairview Ave. N., Seattle, WA, 19024, USA.
Ben StaalVan Andel Institute, 333 Bostwick NE, Grand Rapids, MI, 49503, USA.
Maneesh JainUniversity of Nebraska Medical Center, 42nd and Emile Streets, Omaha, NE, 68198, USA.
Johannes FahrmannMD Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX, 77030, USA.
Christine WorthingtonUniversity of Pittsburgh Medical Center, 200 Lothrop St., Pittsburgh, PA, 15213-2582, USA.
Denise ProsserUniversity of Pittsburgh Medical Center, 200 Lothrop St., Pittsburgh, PA, 15213-2582, USA.
Liudmila VelokokhatnayaUniversity of Pittsburgh Medical Center, 200 Lothrop St., Pittsburgh, PA, 15213-2582, USA.
Camden LopezFred Hutchinson Cancer Research Center, 1100 Fairview Ave. N., Seattle, WA, 19024, USA.
Runlong TangFred Hutchinson Cancer Research Center, 1100 Fairview Ave. N., Seattle, WA, 19024, USA.
Mark W HurdMD Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX, 77030, USA.
Gopalakrishnan NatarajanUniversity of Nebraska Medical Center, 42nd and Emile Streets, Omaha, NE, 68198, USA.
Sushil KumarUniversity of Nebraska Medical Center, 42nd and Emile Streets, Omaha, NE, 68198, USA.
Lynette SmithUniversity of Nebraska Medical Center, 42nd and Emile Streets, Omaha, NE, 68198, USA.
Sam HanashMD Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX, 77030, USA.
Surinder K BatraUniversity of Nebraska Medical Center, 42nd and Emile Streets, Omaha, NE, 68198, USA.
Anirban MaitraMD Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX, 77030, USA.
Anna LokshinUniversity of Pittsburgh Medical Center, 200 Lothrop St., Pittsburgh, PA, 15213-2582, USA.
Ying HuangFred Hutchinson Cancer Research Center, 1100 Fairview Ave. N., Seattle, WA, 19024, USA.
Randall E BrandUniversity of Pittsburgh Medical Center, 200 Lothrop St., Pittsburgh, PA, 15213-2582, USA. Electronic address: brandre@upmc.edu.

Funding

The Early Detection Research Network: Data Management and Coordinating CenterU24CA086368 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI RUTH D ETZIONI, Ziding Feng · 2010 to 2026
$75.7M
Validation of biomarkers for risk prediction and early diagnosis of Pancreatic AdenocarcinomaU01CA200466 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Surinder K. Batra, Randall Brand · 2016 to 2026
$11.3M
Project 3: Inhibiting Oxidative Phosphorylation in Pancreatic CancerP50CA221707 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KOPETZ, SCOTT, MAITRA, ANIRBAN · 2019 to 2023
$11.0M
Clinical Validation Center for Early Detection of Pancreatic CancerU01CA200468 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ANIRBAN MAITRA · 2016 to 2026
$11.0M
Detection of Pre-Invasive Pancreatic Cysts Using Protein and Glycan BiomarkersU01CA152653 · NCI · VAN ANDEL RESEARCH INSTITUTE · PI ALLEN, PETER J, BRAND, RANDALL · 2010 to 2021
$5.8M
Subpopulations of Pancreatic Cancer Cells Defined by Glycan MarkersU01CA226158 · NCI · VAN ANDEL RESEARCH INSTITUTE · PI BRAND, RANDALL, HAAB, BRIAN B. · 2019 to 2023
$3.2M
Accelerating biomarker development through novel statistical methods for analyzing phase III/IV studiesR01CA277133 · NCI · FRED HUTCHINSON CANCER CENTER · PI Ying Huang · 2023 to 2026
$1.6M
NCI NIH HHS P50 CA221707NCI NIH HHS R01 CA277133NCI NIH HHS U01 CA152653NCI NIH HHS U01 CA200466NCI NIH HHS U01 CA200468NCI NIH HHS U01 CA226158NCI NIH HHS U24 CA086368
6 · The paper itself

Abstract

A blood test that enables surveillance for early-stage pancreatic ductal adenocarcinoma (PDAC) is an urgent need. Independent laboratories have reported PDAC biomarkers that could improve biomarker performance over CA19-9 alone, but the performance of the previously reported biomarkers in combination is not known. Therefore, we conducted a coordinated case/control study across multiple laboratories using common sets of blinded training and validation samples (132 and 295 plasma samples, respectively) from PDAC patients and non-PDAC control subjects representing conditions under which surveillance occurs. We analyzed the training set to identify candidate biomarker combination panels using biomarkers across laboratories, and we applied the fixed panels to the validation set. The panels identified in the training set, CA19-9 with CA199.STRA, LRG1, TIMP-1, TGM2, THSP2, ANG, and MUC16.STRA, achieved consistent performance in the validation set. The panel of CA19-9 with the glycan biomarker CA199.STRA improved sensitivity from 0.44 with 0.98 specificity for CA19-9 alone to 0.71 with 0.98 specificity (p < 0.001, 1000-fold bootstrap). Similarly, CA19-9 combined with the protein biomarker LRG1 and CA199.STRA improved specificity from 0.16 with 0.94 sensitivity for CA19-9 to 0.65 with 0.89 sensitivity (p < 0.001, 1000-fold bootstrap). We further validated significantly improved performance using biomarker panels that did not include CA19-9. This study establishes the effectiveness of a coordinated study of previously discovered biomarkers and identified panels of those biomarkers that significantly increased the sensitivity and specificity of early-stage PDAC detection in a rigorous validation trial.

Indexed as

Biomarkers, TumorCA-19-9 AntigenCarcinoma, Pancreatic DuctalPancreatic NeoplasmsAgedAntigens, Tumor-Associated, CarbohydrateCase-Control StudiesFemaleHumansMaleMiddle AgedSensitivity and SpecificityAntigens, Tumor-Associated, CarbohydrateBiomarkers, TumorCA-19-9 Antigencarbohydrate antigen 199, humanBiomarkersCA 19–9Early detectionPancreatic adenocarcinomaPanel

Identifiers

PMID39276915
PMCPMC11808537

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Registered trials

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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.