Evidence map›Paper›PMID 25798586›Full record

ArticlePloS one2015

Personalized oncogenomics: clinical experience with malignant peritoneal mesothelioma using whole genome sequencing.

Brandon S Sheffield, Anna V Tinker, Yaoqing Shen, Harry Hwang, Hector H Li-Chang, Erin Pleasance, Carolyn Ch'ng, Amy Lum, Julie Lorette, Yarrow J McConnell and 9 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

22 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
  3. Molecular characterization of diffuse malignant peritoneal mesothelioma.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2020
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  10. Review
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  12. Article
  13. Temporal Dynamics of Genomic Alterations in aJCO precision oncology · 2018
    Article
  14. Article
  15. Article
  16. Review
  17. Investigation of PD-L1 Biomarker Testing Methods for PD-1 Axis Inhibition in Non-squamous Non-small Cell Lung Cancer.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2016
    Article
  18. Review
  19. Article
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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

19 authors at 3 institutions in 1 country.

Brandon S SheffieldUniversity of British Columbia, Department of Pathology and Laboratory Medicine, Vancouver, Canada.
Anna V TinkerBritish Columbia Cancer Agency, Division of Medical Oncology, Vancouver Centre, Vancouver, Canada.
Yaoqing ShenCanada's Michael Smith Genome Sciences Centre, British Columbia Cancer Agency, Vancouver, Canada.
Harry HwangPhenoPath Laboratories, Seattle, Washington, United States of America.
Hector H Li-ChangUniversity of British Columbia, Department of Pathology and Laboratory Medicine, Vancouver, Canada.
Erin PleasanceCanada's Michael Smith Genome Sciences Centre, British Columbia Cancer Agency, Vancouver, Canada.
Carolyn Ch'ngCanada's Michael Smith Genome Sciences Centre, British Columbia Cancer Agency, Vancouver, Canada.
Amy LumUniversity of British Columbia, Department of Pathology and Laboratory Medicine, Vancouver, Canada.
Julie LoretteUniversity of British Columbia, Department of Pathology and Laboratory Medicine, Vancouver, Canada.
Yarrow J McConnellUniversity of British Columbia, Department of Surgery, Surgical Oncology, Vancouver, Canada.
Sophie SunBritish Columbia Cancer Agency, Division of Medical Oncology, Vancouver Centre, Vancouver, Canada.
Steven J M JonesCanada's Michael Smith Genome Sciences Centre, British Columbia Cancer Agency, Vancouver, Canada.
Allen M GownUniversity of British Columbia, Department of Pathology and Laboratory Medicine, Vancouver, Canada; PhenoPath Laboratories, Seattle, Washington, United States of America.
David G HuntsmanUniversity of British Columbia, Department of Pathology and Laboratory Medicine, Vancouver, Canada.
David F SchaefferUniversity of British Columbia, Department of Pathology and Laboratory Medicine, Vancouver, Canada.
Andrew ChurgUniversity of British Columbia, Department of Pathology and Laboratory Medicine, Vancouver, Canada.
Stephen YipUniversity of British Columbia, Department of Pathology and Laboratory Medicine, Vancouver, Canada.
Janessa LaskinBritish Columbia Cancer Agency, Division of Medical Oncology, Vancouver Centre, Vancouver, Canada.
Marco A MarraCanada's Michael Smith Genome Sciences Centre, British Columbia Cancer Agency, Vancouver, Canada.
University of British Columbia · CACanada's Michael Smith Genome Sciences Centre · CABC Cancer Agency · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peritoneal mesothelioma is a rare and sometimes lethal malignancy that presents a clinical challenge for both diagnosis and management. Recent studies have led to a better understanding of the molecular biology of peritoneal mesothelioma. Translation of the emerging data into better treatments and outcome is needed. From two patients with peritoneal mesothelioma, we derived whole genome sequences, RNA expression profiles, and targeted deep sequencing data. Molecular data were made available for translation into a clinical treatment plan. Treatment responses and outcomes were later examined in the context of molecular findings. Molecular studies presented here provide the first reported whole genome sequences of peritoneal mesothelioma. Mutations in known mesothelioma-related genes NF2, CDKN2A, LATS2, amongst others, were identified. Activation of MET-related signaling pathways was demonstrated in both cases. A hypermutated phenotype was observed in one case (434 vs. 18 single nucleotide variants) and was associated with a favourable outcome despite sarcomatoid histology and multifocal disease. This study represents the first report of whole genome analyses of peritoneal mesothelioma, a key step in the understanding and treatment of this disease.

Indexed as

Genes, Neurofibromatosis 2Genome, HumanAdultBiomarkers, TumorCyclin-Dependent Kinase Inhibitor p16FemaleGenome-Wide Association StudyHigh-Throughput Nucleotide SequencingHumansMesotheliomaMiddle AgedPeritoneal NeoplasmsPrecision MedicinePrognosisProtein Serine-Threonine KinasesTumor Suppressor ProteinsBiomarkers, TumorCyclin-Dependent Kinase Inhibitor p16LATS2 protein, humanProtein Serine-Threonine KinasesTumor Suppressor Proteins

Identifiers

PMID25798586
PMCPMC4370594
OpenAlexW1997207382

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.