Evidence map›Paper›PMID 33028596›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2020

Effect of Germline Mutations in Homologous Recombination Repair Genes on Overall Survival of Patients with Pancreatic Adenocarcinoma.

Siddhartha Yadav, Pashtoon M Kasi, William R Bamlet, Thanh P Ho, Eric C Polley, Chunling Hu, Steven N Hart, Kari G Rabe, Nicholas J Boddicker, Rohan D Gnanaolivu and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 2 pooled it
2.2field-weighted citation impact, top 10% of its field
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

26 citing papers in PubMed, 2 syntheses or guidelines pooled it, 41 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Article
  4. Article
  5. Genomic and Immune Landscape of Pancreatic Ductal Adenocarcinoma Associated with Germline Pathogenic Variants in ATM.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  6. Review
  7. Article
  8. Review
  9. Germline-Somatic Interactions in BRCA-Associated Cancers: Unique Molecular Profiles and Clinical Outcomes Linking ATM to TP53 Synthetic Essentiality.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Homologous Recombination Deficiencies and Hereditary Tumors.International journal of molecular sciences · 2021
    Review
  19. Article
  20. 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

15 authors at 2 institutions in 1 country.

Siddhartha Yadav *Department of Oncology, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0003-4630-9903
Pashtoon M Kasi *Department of Internal Medicine, University of Iowa, Iowa City, Iowa.ORCID 0000-0002-5169-7085
William R BamletDepartment of Health Sciences Research, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0003-2903-1284
Thanh P HoDepartment of Oncology, Mayo Clinic, Rochester, Minnesota.
Eric C PolleyDepartment of Health Sciences Research, Mayo Clinic, Rochester, Minnesota.
Chunling HuDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
Steven N HartDepartment of Health Sciences Research, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0001-7714-2734
Kari G RabeDepartment of Health Sciences Research, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0002-7313-1875
Nicholas J BoddickerDepartment of Health Sciences Research, Mayo Clinic, Rochester, Minnesota.
Rohan D GnanaolivuDepartment of Health Sciences Research, Mayo Clinic, Rochester, Minnesota.
Kun Y LeeDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0002-0684-8112
Tricia H LindstromDepartment of Health Sciences Research, Mayo Clinic, Rochester, Minnesota.
Gloria M PetersenDepartment of Health Sciences Research, Mayo Clinic, Rochester, Minnesota.
Fergus J CouchDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
Robert R McWilliamsDepartment of Oncology, Mayo Clinic, Rochester, Minnesota. McWilliams.Robert@mayo.edu.
Mayo Clinic · USUniversity of Iowa · US

Funding

The Role of CHFR in Tumorigenesis and Paclitaxel-Sensitivity in Breast CancerP50CA116201 · NCI · MAYO CLINIC ROCHESTER · PI PETER C LUCAS · 2005 to 2026
$49.9M
Tissue CoreP50CA102701 · NCI · MAYO CLINIC ROCHESTER · PI COHEN, PETER A · 2004 to 2018
$32.7M
Risk and penetrance of mutations from breast cancer testing panels.R01CA192393 · NCI · MAYO CLINIC ROCHESTER · PI COUCH, FERGUS JOSEPH, NATHANSON, KATHERINE L. · 2014 to 2018
$6.3M
Identifying and validating novel susceptibility genes for breast cancerR01CA176785 · NCI · MAYO CLINIC ROCHESTER · PI COUCH, FERGUS JOSEPH, NATHANSON, KATHERINE L. · 2014 to 2018
$3.4M
BRCA2 missense mutations and breast cancerR01CA116167 · NCI · MAYO CLINIC ROCHESTER · PI COUCH, FERGUS JOSEPH · 2007 to 2011
$3.0M
BRCA1 and BRCA2 missense mutations and breast cancer riskU01CA116167 · NCI · MAYO CLINIC ROCHESTER · PI COUCH, FERGUS JOSEPH · 2013 to 2017
$2.7M
The contribution of RAD51C and RAD51D to breast and ovarian cancerR01CA225662 · NCI · MAYO CLINIC ROCHESTER · PI COUCH, FERGUS JOSEPH, WEROHA, SARAVUT · 2018 to 2024
$2.5M
Role of Vav1 protooncogene in pancreatic cancerP20CA102701 · NCI · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI PETERSEN, GLORIA M. · 2003 to 2003
$1.5M
NCI NIH HHS P20 CA102701NCI NIH HHS P50 CA102701NCI NIH HHS P50 CA116201NCI NIH HHS R01 CA116167NCI NIH HHS R01 CA176785NCI NIH HHS R01 CA192393NCI NIH HHS R01 CA225662NCI NIH HHS U01 CA116167
6 · The paper itself

Abstract

purposeTo compare the clinical characteristics and overall survival (OS) of germline mutation carriers in homologous recombination repair (HRR) genes and noncarriers with pancreatic ductal adenocarcinoma (PDAC). EXPERIMENTAL

designGermline DNA from 3,078 patients with PDAC enrolled in a prospective registry at Mayo Clinic between 2000 and 2017 was analyzed for mutations in 37 cancer predisposition genes. Characteristics and OS of patients with mutations in eight genes

resultsThe 175 HRR mutation carriers and 2,730 noncarriers in the study had a median duration of follow-up of 9.9 years. HRR mutation carriers were younger (median age at diagnosis: 63 vs. 66 years,

conclusionsThis study demonstrates that germline mutation carrier status in PDAC is associated with longer OS compared with noncarriers. Further research into tumor biology and response to platinum-based chemotherapy in germline mutation carriers with PDAC are needed to better understand the association with longer OS.

Indexed as

Germ-Line MutationRecombinational DNA RepairAdenocarcinomaAgedBiomarkers, TumorDNA Repair EnzymesFemaleFollow-Up StudiesGenetic TestingHumansMaleMiddle AgedPancreatic NeoplasmsPrognosisProspective StudiesSurvival RateBiomarkers, TumorDNA Repair Enzymes

Identifiers

PMID33028596
PMCPMC9063708
OpenAlexW3091797030

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.