Evidence map›Paper›PMID 37556141›Full record

ArticleJAMA network open2023

Germline Variants Incidentally Detected via Tumor-Only Genomic Profiling of Patients With Mesothelioma.

Owen D Mitchell, Katie Gilliam, Daniela Del Gaudio, Kelsey E McNeely, Shaili Smith, Maria Acevedo, Meghana Gaduraju, Rachel Hodge, Aubrianna S S Ramsland, Jeremy Segal and 15 more

Open access · goldAbstract read
In one paragraph

Article in JAMA network open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Clinical and Pathologic Phenotyping of Mesotheliomas Developing in Carriers of Germline BAP1 Mutations.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2025
    Article
  4. Article
  5. Review
  6. Radiomics for differentiation of somaticJournal of medical imaging (Bellingham, Wash.) · 2024
    Article
  7. GermlineProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Review
  9. Review
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

25 authors at 2 institutions in 1 country.

Owen D MitchellSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Illinois.
Katie GilliamSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Illinois.
Daniela Del GaudioDepartment of Human Genetics, The University of Chicago, Illinois.
Kelsey E McNeelySection of Hematology/Oncology, Department of Medicine, The University of Chicago, Illinois.
Shaili SmithSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Illinois.
Maria AcevedoSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Illinois.
Meghana GadurajuSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Illinois.
Rachel HodgeSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Illinois.
Aubrianna S S RamslandSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Illinois.
Jeremy SegalDepartment of Pathology, The University of Chicago, Illinois.
Soma DasDepartment of Human Genetics, The University of Chicago, Illinois.
Feighanne HathawaySection of Hematology/Oncology, Department of Medicine, The University of Chicago, Illinois.
Darren S BryanDepartment of Surgery, The University of Chicago, Illinois.
Sanjukta TawdeDepartment of Human Genetics, The University of Chicago, Illinois.
Shelly GalasinskiDepartment of Human Genetics, The University of Chicago, Illinois.
Peng WangDepartment of Pathology, The University of Chicago, Illinois.
Melissa Y TjotaDepartment of Pathology, The University of Chicago, Illinois.
Aliya N HusainDepartment of Pathology, The University of Chicago, Illinois.
Samuel G ArmatoDepartment of Radiology, The University of Chicago, Illinois.
Jessica DoningtonDepartment of Surgery, The University of Chicago, Illinois.
Mark K FergusonDepartment of Surgery, The University of Chicago, Illinois.
Kiran TuragaDepartment of Surgery, The University of Chicago, Illinois.
Jane E ChurpekDivision of Hematology, Medical Oncology, and Palliative Care, Department of Medicine, University of Wisconsin, Madison.
Hedy L KindlerSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Illinois.
Michael W DrazerSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Illinois.
University of Chicago · USUniversity of Wisconsin–Madison · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Patients with mesothelioma often have next-generation sequencing (NGS) of their tumor performed; tumor-only NGS may incidentally identify germline pathogenic or likely pathogenic (P/LP) variants despite not being designed for this purpose. It is unknown how frequently patients with mesothelioma have germline P/LP variants incidentally detected via tumor-only NGS. Objective: To determine the prevalence of incidental germline P/LP variants detected via tumor-only NGS of mesothelioma. Design, Setting, and Participants: A series of 161 unrelated patients with mesothelioma from a high-volume mesothelioma program had tumor-only and germline NGS performed during April 2016 to October 2021. Follow-up ranged from 18 months to 7 years. Tumor and germline assays were compared to determine which P/LP variants identified via tumor-only NGS were of germline origin. Data were analyzed from January to March 2023. Main Outcomes and Measures: The proportion of patients with mesothelioma who had P/LP germline variants incidentally detected via tumor-only NGS. Results: Of 161 patients with mesothelioma, 105 were male (65%), the mean (SD) age was 64.7 (11.2) years, and 156 patients (97%) self-identified as non-Hispanic White. Most (126 patients [78%]) had at least 1 potentially incidental P/LP germline variant. The positive predictive value of a potentially incidental germline P/LP variant on tumor-only NGS was 20%. Overall, 26 patients (16%) carried a P/LP germline variant. Germline P/LP variants were identified in ATM, ATR, BAP1, CHEK2, DDX41, FANCM, HAX1, MRE11A, MSH6, MUTYH, NF1, SAMD9L, and TMEM127. Conclusions and Relevance: In this case series of 161 patients with mesothelioma, 16% had confirmed germline P/LP variants. Given the implications of a hereditary cancer syndrome diagnosis for preventive care and familial counseling, clinical approaches for addressing incidental P/LP germline variants in tumor-only NGS are needed. Tumor-only sequencing should not replace dedicated germline testing. Universal germline testing is likely needed for patients with mesothelioma.

Indexed as

MesotheliomaMesothelioma, MalignantAdaptor Proteins, Signal TransducingDNA HelicasesFemaleGenetic Predisposition to DiseaseGenomicsHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedAdaptor Proteins, Signal TransducingDNA HelicasesFANCM protein, humanHAX1 protein, human

Identifiers

PMID37556141
PMCPMC10413174
OpenAlexW4385684767

What OpenQuestion holds

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LicenceCC BY
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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.