Evidence map›Paper›PMID 33402737›Full record

ArticleBritish journal of cancer2021

The mutational load and a T-cell inflamed tumour phenotype identify ovarian cancer patients rendering tumour-reactive T cells from PD-1

Diego Salas-Benito, Enrique Conde, Ibon Tamayo-Uria, Uxua Mancheño, Edurne Elizalde, David Garcia-Ros, Jose M Aramendia, Juan C Muruzabal, Julia Alcaide, Francisco Guillen-Grima and 8 more

Abstract read
In one paragraph

Article in British journal of cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Trial
  2. Article
  3. Composite score of PD-1Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2025
    Article
  4. Article
  5. Article
  6. Observational
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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

18 authors.

Diego Salas-BenitoDepartment of Medical Oncology, Clínica Universidad de Navarra, Pamplona, Spain.ORCID http://orcid.org/0000-0002-8995-1499
Enrique CondeInstituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.ORCID http://orcid.org/0000-0002-3587-1506
Ibon Tamayo-UriaInstituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.ORCID http://orcid.org/0000-0002-8183-7106
Uxua MancheñoInstituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.ORCID http://orcid.org/0000-0003-1533-0371
Edurne ElizaldeInstituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
David Garcia-RosInstituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
Jose M AramendiaDepartment of Medical Oncology, Clínica Universidad de Navarra, Pamplona, Spain.ORCID http://orcid.org/0000-0002-6417-4267
Juan C MuruzabalInstituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.ORCID http://orcid.org/0000-0001-9829-3435
Julia AlcaideDepartment of Oncology, Hospital Costa del Sol, Marbella, Spain.ORCID http://orcid.org/0000-0002-9301-1387
Francisco Guillen-GrimaInstituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.ORCID http://orcid.org/0000-0001-9749-8076
Jose A MinguezDepartment of Medical Oncology, Clínica Universidad de Navarra, Pamplona, Spain.
Jose Amores-TiradoDepartment of Gynecology, Hospital Costa del Sol, Marbella, Spain.
Antonio Gonzalez-MartinDepartment of Medical Oncology, Clínica Universidad de Navarra, Pamplona, Spain.
Pablo SarobeInstituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
Juan J LasarteInstituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
Mariano Ponz-SarviseDepartment of Medical Oncology, Clínica Universidad de Navarra, Pamplona, Spain. mponz@unav.es.ORCID http://orcid.org/0000-0002-3240-729X
Carlos E De Andrea *Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
Sandra Hervas-Stubbs *Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain. mshervas@unav.es.ORCID http://orcid.org/0000-0003-3391-1516

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdoptive immunotherapy with tumour-infiltrating lymphocytes (TIL) may benefit from the use of selective markers, such as PD-1, for tumour-specific T-cell enrichment, and the identification of predictive factors that help identify those patients capable of rendering tumour-reactive TILs. We have investigated this in ovarian cancer (OC) patients as candidates for TIL therapy implementation.

methodsPD-1

resultsTumour-reactive TILs were detected in half of patients and were exclusively present in cells derived from the PD-1

conclusionWe have demonstrated that PD-1 identifies ovarian tumour-specific CD8 TILs and has uncovered predictive factors that identify OC patients who are likely to render tumour-specific cells from PD-1

Indexed as

Gene Expression Regulation, NeoplasticBiomarkers, TumorCD8-Positive T-LymphocytesFemaleFollow-Up StudiesHumansLymphocytes, Tumor-InfiltratingOvarian NeoplasmsPhenotypePrognosisProgrammed Cell Death 1 ReceptorRetrospective StudiesBiomarkers, TumorPDCD1 protein, humanProgrammed Cell Death 1 Receptor

Identifiers

PMID33402737
PMCPMC7961070

What OpenQuestion holds

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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.