Evidence map›Paper›PMID 30987368›Full record

ReviewInternational journal of molecular sciences2019

Targeting the PD-1/PD-L1 Pathway in Renal Cell Carcinoma.

Solène-Florence Kammerer-Jacquet, Antoine Deleuze, Judikaël Saout, Romain Mathieu, Brigitte Laguerre, Gregory Verhoest, Frédéric Dugay, Marc-Antoine Belaud-Rotureau, Karim Bensalah, Nathalie Rioux-Leclercq

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 3 pooled it
–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

51 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Guideline
  4. Trial
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  6. Review
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  14. GPCRs: emerging targets for novel T cell immune checkpoint therapy.Cancer immunology, immunotherapy : CII · 2024
    Review
  15. Article
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  19. Article
  20. Cancer Cell-Derived PDGFB Stimulates mTORC1 Activation in Renal Carcinoma.International journal of molecular sciences · 2023
    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

10 authors.

Solène-Florence Kammerer-JacquetDepartment of Pathology, University Hospital, 35000 Rennes, France. jacquet.sf@gmail.com.
Antoine DeleuzeDepartment of Medical Oncology, Centre Eugene Marquis, 35000 Rennes, France. acjdeleuze@gmail.com.
Judikaël SaoutUniversité Rennes, Inserm, EHESP (Ecole des Hautes Etudes en Santé Publique), Irset (Institut de recherche en santé, environnement et travail) - UMR_S 1085, F-35000 Rennes, France. judikael.saout@univ-rennes1.fr.
Romain MathieuUniversité Rennes, Inserm, EHESP (Ecole des Hautes Etudes en Santé Publique), Irset (Institut de recherche en santé, environnement et travail) - UMR_S 1085, F-35000 Rennes, France. romain.mathieu@chu-rennes.fr.
Brigitte LaguerreDepartment of Medical Oncology, Centre Eugene Marquis, 35000 Rennes, France. b.laguerre@rennes.unicancer.fr.
Gregory VerhoestDepartment of Urology, University Hospital, 35000 Rennes, France. gregory.verhoest@chu-rennes.fr.
Frédéric DugayUniversité Rennes, Inserm, EHESP (Ecole des Hautes Etudes en Santé Publique), Irset (Institut de recherche en santé, environnement et travail) - UMR_S 1085, F-35000 Rennes, France. frederic.dugay@chu-rennes.fr.
Marc-Antoine Belaud-RotureauUniversité Rennes, Inserm, EHESP (Ecole des Hautes Etudes en Santé Publique), Irset (Institut de recherche en santé, environnement et travail) - UMR_S 1085, F-35000 Rennes, France. marc-antoine.belaud-rotureau@chu-rennes.fr.
Karim BensalahDepartment of Urology, University Hospital, 35000 Rennes, France. karim.bensalah@chu-rennes.fr.
Nathalie Rioux-LeclercqDepartment of Pathology, University Hospital, 35000 Rennes, France. nathalie.rioux-leclercq@chu-rennes.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal cell carcinoma encompass distinct diseases with different pathologic features and distinct molecular pathways. Immune checkpoint inhibitors targeting the programmed death receptor ligand 1 (PD-L1)/programmed death receptor 1 (PD-1) pathway alone or in combination have greatly changed clinical management of metastatic renal cell carcinoma, now competing with antiangiogenic drugs in monotherapy for first-line treatment. However, long-term response rates are low, and biomarkers are needed to predict treatment response. Quantification of PD-L1 expression by immunohistochemistry was developed as a promising biomarker in clinical trials, but with many limitations (different antibodies, tumour heterogeneity, specimens, and different thresholds of positivity). Other biomarkers, including tumour mutational burden and molecular signatures, are also developed and discussed in this review.

Indexed as

AnimalsBiomarkers, TumorCarcinoma, Renal CellHumansImmunotherapyProgrammed Cell Death 1 ReceptorBiomarkers, TumorPDCD1 protein, humanProgrammed Cell Death 1 Receptorbiomarkerimmune checkpoint inhibitionimmunotherapyPD-1PD-L1renal cell carcinomatumour mutational burden

Identifiers

PMID30987368
PMCPMC6480014

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.