Evidence map›Paper›PMID 32376723›Full record

ArticleJournal for immunotherapy of cancer2020

Oncogenic states dictate the prognostic and predictive connotations of intratumoral immune response.

Jessica Roelands, Wouter Hendrickx, Gabriele Zoppoli, Raghvendra Mall, Mohamad Saad, Kyle Halliwill, Giuseppe Curigliano, Darawan Rinchai, Julie Decock, Lucia G Delogu and 13 more

Erratum issuedAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 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

64 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  8. The diversity of CD8Nature reviews. Immunology · 2025
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4 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors.

Jessica Roelands *Cancer Research Department, Research Branch, Sidra Medicine, Doha, Qatar.ORCID 0000-0003-3631-2041
Wouter Hendrickx *Cancer Research Department, Research Branch, Sidra Medicine, Doha, Qatar wouterhendrickx79@gmail.com dbedognetti@sidra.org m.ceccarelli@gmail.com.
Gabriele ZoppoliIRCCS Ospedale Policlinico San Martino, Genova, Italy.
Raghvendra MallQatar Computing Research Institute (QCRI), Hamad Bin Khalifa University (HBKU), Doha, Qatar.
Mohamad SaadQatar Computing Research Institute (QCRI), Hamad Bin Khalifa University (HBKU), Doha, Qatar.
Kyle HalliwillGenomics Research Center (GRC), AbbVie Biotherapeutics, Redwood City, California, USA.
Giuseppe CuriglianoDepartment of Oncology and Hemato-Oncology, University of Milano, Milano, Italy.
Darawan RinchaiCancer Research Department, Research Branch, Sidra Medicine, Doha, Qatar.
Julie Decock
Lucia G DeloguIstituto di Ricerca Pediatrica, Fondazione Città della Speranza, Padua, Italy.
Tolga TuranGenomics Research Center (GRC), AbbVie Biotherapeutics, Redwood City, California, USA.ORCID 0000-0002-3333-3851
Josue SamayoaGenomics Research Center (GRC), AbbVie Biotherapeutics, Redwood City, California, USA.
Lotfi Chouchane
Alberto BallestreroIRCCS Ospedale Policlinico San Martino, Genova, Italy.
Ena Wang
Pascal Finetti
Francois Bertucci
Lance D Miller
Jerome Galon
Francesco M Marincola
Peter J K KuppenDepartment of Surgery, Leiden University Medical Center (LUMC), Leiden, The Netherlands.
Michele CeccarelliGenomics Research Center (GRC), AbbVie Biotherapeutics, Redwood City, California, USA wouterhendrickx79@gmail.com dbedognetti@sidra.org m.ceccarelli@gmail.com.
Davide BedognettiCancer Research Department, Research Branch, Sidra Medicine, Doha, Qatar wouterhendrickx79@gmail.com dbedognetti@sidra.org m.ceccarelli@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAn immune active cancer phenotype typified by a T helper 1 (Th-1) immune response has been associated with increased responsiveness to immunotherapy and favorable prognosis in some but not all cancer types. The reason of this differential prognostic connotation remains unknown.

methodsTo explore the contextual prognostic value of cancer immune phenotypes, we applied a multimodal pan-cancer analysis among 31 different histologies (9282 patients), encompassing immune and oncogenic transcriptomic analysis, mutational and neoantigen load and copy number variations.

resultsWe demonstrated that the favorable prognostic connotation conferred by the presence of a Th-1 immune response was abolished in tumors displaying specific tumor-cell intrinsic attributes such as high transforming growth factor-beta (TGF-β) signaling and low proliferation capacity. This observation was independent of mutation rate. We validated this observation in the context of immune checkpoint inhibition. WNT-

conclusionsThis is the first systematic study demonstrating that the prognostic and predictive role of a bona fide favorable intratumoral immune response is dependent on the disposition of specific oncogenic pathways. This information could be used to refine stratification algorithms and prioritize hierarchically relevant targets for combination therapies.

Indexed as

FemaleGene Expression ProfilingHumansImmunityImmunotherapyMaleNeoplasmsOncogenesPrognosisSurvival Analysiscytotoxicity, immunologicgene expression profilinggenetic markersgenome Instabilityimmunotherapy

Identifiers

PMID32376723
PMCPMC7223637

What OpenQuestion holds

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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.