Evidence map›Paper›PMID 34589950›Full record

ArticleJTO clinical and research reports2020

Somatic and Germline BRCA 1 and 2 Mutations in Advanced NSCLC From the SAFIR02-Lung Trial.

Jordi Remon, Benjamin Besse, Alexandra Leary, Ivan Bièche, Bastien Job, Ludovic Lacroix, Aurélie Auguste, Marjorie Mauduit, Clarisse Audigier-Valette, Judith Raimbourg and 7 more

Open access · goldAbstract read
In one paragraph

Article in JTO clinical and research reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. International journal of molecular sciences · 2026
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Translational lung cancer research · 2023
    Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Lung cancer is also a hereditary disease.European respiratory review : an official journal of the European Respiratory Society · 2021
    Review
  19. 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

17 authors at 8 institutions in 1 country.

Jordi RemonCancer Medicine Department, Gustave Roussy, Villejuif, France.
Benjamin BesseCancer Medicine Department, Gustave Roussy, Villejuif, France.
Alexandra LearyCancer Medicine Department, Gustave Roussy, Villejuif, France.
Ivan BiècheService de Génétique, Institut Curie, Paris, France.
Bastien JobLaboratoire de Recherche Translationnelle, AMMICA, INSERM US23/CNRS UNS3655, Gustave Roussy, Villejuif, France.
Ludovic LacroixLaboratoire de Recherche Translationnelle, AMMICA, INSERM US23/CNRS UNS3655, Gustave Roussy, Villejuif, France.
Aurélie AugusteService de Génétique des Tumeurs, Département de Biologie et Pathologie Médicale, INSERM U981, Gustave Roussy, Villejuif, France.
Marjorie MauduitUnicancer, Paris, France.
Clarisse Audigier-ValettePneumology Department, CHI Toulon, France.
Judith RaimbourgOncology Department, Institut de Cancérologie de l'Ouest, Nantes, France.
Anne MadroszykPneumology Department, Institut Paoli Calmettes, Marseille, France.
Stefan MichelsService de Biostatistics and Epidemiology, Gustave Roussy and CESP, INSERM, University Paris-Saclay, Villejuif, France.
Mohammed Amine BayarService de Biostatistics and Epidemiology, Gustave Roussy and CESP, INSERM, University Paris-Saclay, Villejuif, France.
Marta JimenezUnicancer, Paris, France.
Jean-Charles SoriaCancer Medicine Department, Gustave Roussy, Villejuif, France.
Etienne RouleauService de Génétique des Tumeurs, Département de Biologie et Pathologie Médicale, INSERM U981, Gustave Roussy, Villejuif, France.
Fabrice BarlesiCancer Medicine Department, Gustave Roussy, Villejuif, France.
Centre National de la Recherche Scientifique · FRInserm · FRUniCancer Group · FRUniversité Paris-Saclay · FRInstitut Curie · FRInstitut de Cancérologie de l'Ouest · FRInstitut Gustave Roussy · FRInstitut Paoli-Calmettes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMolecular profiling is considered a standard of care in advanced NSCLC. A comprehensive next-generation sequencing panel can discover somatic or germline

methodsFrom April 2014 to March 2017, 600 newly diagnosed,

resultsOf 379 patients with a molecular profile discussed in a tumor molecular board,

conclusionsPathogenic

Indexed as

Advanced non–small cell lung cancerBRCA mutationNext-generation sequencingPARP inhibitorsSAFIR trial

Identifiers

PMID34589950
PMCPMC8474245
OpenAlexW3035698550

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.