Evidence map›Paper›PMID 28487385›Full record

ArticleCancer research2017

Immune-Related Gene Expression Profiling After PD-1 Blockade in Non-Small Cell Lung Carcinoma, Head and Neck Squamous Cell Carcinoma, and Melanoma.

Aleix Prat, Alejandro Navarro, Laia Paré, Noemí Reguart, Patricia Galván, Tomás Pascual, Alex Martínez, Paolo Nuciforo, Laura Comerma, Llucia Alos and 10 more

Abstract read
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In one paragraph

Article in Cancer research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 282 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
282citing papers in PubMed, 7 pooled it
17.2field-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

282 citing papers in PubMed, 7 syntheses or guidelines pooled it, 468 citations in OpenAlex.

  1. Pooled it
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  13. Randomized Phase II and Biomarker Study of Pembrolizumab plus Bevacizumab versus Pembrolizumab Alone for Patients with Recurrent Glioblastoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Trial
  14. Key regulatory elements of the TGFβ-LRRC15 axis predict disease progression and immunotherapy resistance across cancer types.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  15. Epigenetic plus cytokine therapy induces stem-like CD8Journal for immunotherapy of cancer · 2026
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222 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 2 institutions in 1 country.

Aleix PratTranslational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain. alprat@clinic.cat.
Alejandro NavarroMedical Oncology Department, Vall d'Hebron Hospital, Barcelona, Spain.
Laia ParéTranslational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
Noemí ReguartTranslational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
Patricia GalvánTranslational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
Tomás PascualTranslational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
Alex MartínezMedical Oncology Department, Vall d'Hebron Hospital, Barcelona, Spain.
Paolo NuciforoMolecular Oncology Group, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
Laura ComermaMolecular Oncology Group, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
Llucia AlosPathology Department, Hospital Clínic of Barcelona, Barcelona, Spain.
Nuria PardoMedical Oncology Department, Vall d'Hebron Hospital, Barcelona, Spain.
Susana CedrésMedical Oncology Department, Vall d'Hebron Hospital, Barcelona, Spain.
Cheng FanDepartment of Bioinformatics, Lineberger Comprehensive Cancer Center, Chapel Hill, North Carolina.
Joel S ParkerDepartment of Bioinformatics, Lineberger Comprehensive Cancer Center, Chapel Hill, North Carolina.
Lydia GabaMedical Oncology Department, Hospital Clínic of Barcelona, Barcelona, Spain.
Iván VictoriaMedical Oncology Department, Hospital Clínic of Barcelona, Barcelona, Spain.
Nuria ViñolasMedical Oncology Department, Hospital Clínic of Barcelona, Barcelona, Spain.
Ana VivancosCancer Genomics Group, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
Ana AranceTranslational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
Enriqueta FelipMedical Oncology Department, Vall d'Hebron Hospital, Barcelona, Spain.
CIBBIM-Nanomedicine · ESVall d'Hebron Institute of Oncology

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibody targeting of the immune checkpoint receptor PD1 produces therapeutic activity in a variety of solid tumors, but most patients exhibit partial or complete resistance to treatment for reasons that are unclear. In this study, we evaluated tumor specimens from 65 patients with melanoma, lung nonsquamous, squamous cell lung or head and neck cancers who were treated with the approved PD1-targeting antibodies pembrolizumab or nivolumab. Tumor RNA before anti-PD1 therapy was analyzed on the nCounter system using the PanCancer 730-Immune Panel, and we identified 23 immune-related genes or signatures linked to response and progression-free survival (PFS). In addition, we evaluated intra- and interbiopsy variability of PD1, PD-L1, CD8A, and CD4 mRNAs and their relationship with tumor-infiltrating lymphocytes (TIL) and PD-L1 IHC expression. Among the biomarkers examined, PD1 gene expression along with 12 signatures tracking CD8 and CD4 T-cell activation, natural killer cells, and IFN activation associated significantly with nonprogressive disease and PFS. These associations were independent of sample timing, drug used, or cancer type. TIL correlated moderately (∼0.50) with PD1 and CD8A mRNA levels and weakly (∼0.35) with CD4 and PD-L1. IHC expression of PD-L1 correlated strongly with PD-L1 (0.90), moderately with CD4 and CD8A, and weakly with PD1. Reproducibility of gene expression in intra- and interbiopsy specimens was very high (total SD <3%). Overall, our results support the hypothesis that identification of a preexisting and stable adaptive immune response as defined by mRNA expression pattern is reproducible and sufficient to predict clinical outcome, regardless of the type of cancer or the PD1 therapeutic antibody administered to patients.

Indexed as

AdultAgedAged, 80 and overAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedCarcinoma, Non-Small-Cell LungCarcinoma, Squamous CellFemaleGene ExpressionGene Expression ProfilingHead and Neck NeoplasmsHumansLung NeoplasmsMaleMelanomaMiddle AgedAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedNivolumabPDCD1 protein, humanpembrolizumabProgrammed Cell Death 1 Receptor

Identifiers

PMID28487385
OpenAlexW2613155082

What OpenQuestion holds

Textmetadata
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Registered trials

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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.