Evidence map›Paper›PMID 30316012›Full record

ArticleJournal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer2019

Neoantigenic Potential of Complex Chromosomal Rearrangements in Mesothelioma.

Aaron S Mansfield, Tobias Peikert, James B Smadbeck, Julia B M Udell, Enrique Garcia-Rivera, Laura Elsbernd, Courtney L Erskine, Virginia P Van Keulen, Farhad Kosari, Stephen J Murphy and 16 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed, 1 pooled it
11.9field-weighted citation impact, top 1% 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

79 citing papers in PubMed, 1 synthesis or guideline pooled it, 126 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Review
  6. Moving Beyond Morphology: Toward a Morpho-Molecular Classification of Pleural Mesothelioma.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2026
    Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. CDKN2A deletion is associated with immune desertification in diffuse pleural mesothelioma.Journal of experimental & clinical cancer research : CR · 2025
    Article
  13. Article
  14. Article
  15. Polymeric nanocarriers for therapeutic gene delivery.Asian journal of pharmaceutical sciences · 2025
    Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. Review

19 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors at 3 institutions in 1 country.

Aaron S MansfieldDivision of Medical Oncology, Mayo Clinic, Rochester, Minnesota.
Tobias PeikertDivision of Pulmonary Medicine and Critical Care, Mayo Clinic, Rochester, Minnesota.
James B SmadbeckCenter for Individualized Medicine, Biomarker Discovery Group, Mayo Clinic, Rochester, Minnesota.
Julia B M UdellCenter for International Blood and Marrow Transplant Research, Minneapolis, Minnesota.
Enrique Garcia-Riveranference, Cambridge, Massachusetts.
Laura ElsberndDepartment of Immunology, Mayo Clinic, Rochester, Minnesota.
Courtney L ErskineDepartment of Immunology, Mayo Clinic, Rochester, Minnesota.
Virginia P Van KeulenDepartment of Immunology, Mayo Clinic, Rochester, Minnesota.
Farhad KosariCenter for Individualized Medicine, Biomarker Discovery Group, Mayo Clinic, Rochester, Minnesota.
Stephen J MurphyCenter for Individualized Medicine, Biomarker Discovery Group, Mayo Clinic, Rochester, Minnesota.
Hongzheng RenDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
Vishnu V SerlaCenter for Individualized Medicine, Biomarker Discovery Group, Mayo Clinic, Rochester, Minnesota.
Janet L Schaefer KleinCenter for Individualized Medicine, Biomarker Discovery Group, Mayo Clinic, Rochester, Minnesota.
Giannoula KaragougaCenter for Individualized Medicine, Biomarker Discovery Group, Mayo Clinic, Rochester, Minnesota.
Faye R HarrisCenter for Individualized Medicine, Biomarker Discovery Group, Mayo Clinic, Rochester, Minnesota.
Carlos SosaCenter for Individualized Medicine, Biomarker Discovery Group, Mayo Clinic, Rochester, Minnesota.
Sarah H JohnsonCenter for Individualized Medicine, Biomarker Discovery Group, Mayo Clinic, Rochester, Minnesota.
Wendy NevalaDepartment of Immunology, Mayo Clinic, Rochester, Minnesota.
Svetomir N MarkovicDivision of Medical Oncology, Mayo Clinic, Rochester, Minnesota.
Aaron O BungumDivision of Pulmonary Medicine and Critical Care, Mayo Clinic, Rochester, Minnesota.
Eric S EdellDivision of Pulmonary Medicine and Critical Care, Mayo Clinic, Rochester, Minnesota.
Haidong DongDepartment of Immunology, Mayo Clinic, Rochester, Minnesota; Department of Urology, Mayo Clinic, Rochester, Minnesota.
John C ChevilleDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
Marie Christine AubryDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
Jin JenMedical Genome Facility, Mayo Clinic, Rochester, Minnesota.
George VasmatzisCenter for Individualized Medicine, Biomarker Discovery Group, Mayo Clinic, Rochester, Minnesota. Electronic address: vasmatzis.george@mayo.edu.
Mayo Clinic · USNference (United States) · USWinnMed · US

Funding

Paul Calabresi Program in Clinical/Translational Research at Mayo ClinicK12CA090628 · NCI · MAYO CLINIC ROCHESTER · PI WEROHA, SARAVUT · 2001 to 2025
$19.7M
NCI NIH HHS K12 CA090628
6 · The paper itself

Abstract

introductionMalignant pleural mesothelioma is a disease primarily associated with exposure to the carcinogen asbestos. Whereas other carcinogen-related tumors are associated with a high tumor mutation burden, mesothelioma is not. We sought to resolve this discrepancy.

methodsWe used mate-pair (n = 22), RNA (n = 28), and T cell receptor sequencing along with in silico predictions and immunologic assays to understand how structural variants of chromosomes affect the transcriptome.

resultsWe observed that inter- or intrachromosomal rearrangements were present in every specimen and were frequently in a pattern of chromoanagenesis such as chromoplexy or chromothripsis. Transcription of rearrangement-related junctions was predicted to result in many potential neoantigens, some of which were proven to bind patient-specific major histocompatibility complex molecules and to expand intratumoral T cell clones. T cells responsive to these predicted neoantigens were also present in a patient's circulating T cell repertoire. Analysis of genomic array data from the mesothelioma cohort in The Cancer Genome Atlas suggested that multiple chromothriptic-like events negatively impact survival.

conclusionsOur findings represent the discovery of potential neoantigen expression driven by structural chromosomal rearrangements. These results may have implications for the development of novel immunotherapeutic strategies and the selection of patients to receive immunotherapies.

Indexed as

ChromothripsisAntigensClonal Selection, Antigen-MediatedComputer SimulationDNA, NeoplasmGene DosageGene RearrangementGenomicsHLA-A AntigensHLA-B AntigensHumansLymphocytes, Tumor-InfiltratingMesotheliomaPeptidesPleural NeoplasmsReceptors, Antigen, T-CellAntigensDNA, NeoplasmHLA-A AntigensHLA-B AntigensPeptidesReceptors, Antigen, T-CellChromoplexyChromosomal rearrangementsChromothripsisMesotheliomaNeoantigens

Identifiers

PMID30316012
PMCPMC6348045
OpenAlexW2897816153

What OpenQuestion holds

Textmetadata
LicenceTDM
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.