Evidence map›Paper›PMID 35455739›Full record

ArticleJournal of personalized medicine2022

A Promising Biomarker and Therapeutic Target in Patients with Advanced PDAC: The Stromal Protein βig-h3.

Christelle de la Fouchardière, Pia Gamradt, Sylvie Chabaud, Maxime Raddaz, Ellen Blanc, Olivier Msika, Isabelle Treilleux, Sophie Bachy, Anne Cattey-Javouhey, Pierre Guibert and 10 more

Open access · goldAbstract read
In one paragraph

Article in Journal of personalized medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
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

20 authors at 3 institutions in 1 country.

Christelle de la FouchardièreCancer Research Center of Lyon, UMR INSERM 1052, CNRS 5286, F-69373 Lyon, France.ORCID 0000-0003-2291-5693
Pia GamradtCancer Research Center of Lyon, UMR INSERM 1052, CNRS 5286, F-69373 Lyon, France.ORCID 0000-0002-5567-9722
Sylvie ChabaudCentre Léon Bérard, F-69008 Lyon, France.
Maxime RaddazCentre Léon Bérard, F-69008 Lyon, France.
Ellen BlancCentre Léon Bérard, F-69008 Lyon, France.
Olivier MsikaCentre Léon Bérard, F-69008 Lyon, France.
Isabelle TreilleuxCancer Research Center of Lyon, UMR INSERM 1052, CNRS 5286, F-69373 Lyon, France.
Sophie BachyCancer Research Center of Lyon, UMR INSERM 1052, CNRS 5286, F-69373 Lyon, France.
Anne Cattey-JavouheyCentre Léon Bérard, F-69008 Lyon, France.
Pierre GuibertCentre Léon Bérard, F-69008 Lyon, France.
Matthieu SarabiCancer Research Center of Lyon, UMR INSERM 1052, CNRS 5286, F-69373 Lyon, France.ORCID 0000-0003-4588-0585
Pauline RochefortCentre Léon Bérard, F-69008 Lyon, France.
Pamela Funk-DebledsCentre Léon Bérard, F-69008 Lyon, France.
Clélia CoutzacCancer Research Center of Lyon, UMR INSERM 1052, CNRS 5286, F-69373 Lyon, France.ORCID 0000-0002-8347-6957
Isabelle Ray-CoquardCentre Léon Bérard, F-69008 Lyon, France.ORCID 0000-0003-2472-8306
Patrice PeyratCentre Léon Bérard, F-69008 Lyon, France.
Pierre MeeusCentre Léon Bérard, F-69008 Lyon, France.
Michel RivoireCancer Research Center of Lyon, UMR INSERM 1052, CNRS 5286, F-69373 Lyon, France.
Aurélien DupréCancer Research Center of Lyon, UMR INSERM 1052, CNRS 5286, F-69373 Lyon, France.ORCID 0000-0002-5216-538X
Ana HenninoCancer Research Center of Lyon, UMR INSERM 1052, CNRS 5286, F-69373 Lyon, France.
Centre Léon Bérard · FRUniversité Claude Bernard Lyon 1 · FRCentre National de la Recherche Scientifique · FR

Funding

Association de Recherche sur le Cancer ARC 2017Bristol Meyers Squibb Foundation 2018Centre Léon Berard C442Fondation de France 2019French National Cancer Institute AAP 2019INSERM TRANSFERT 2018Sanofi iAwards 2018
6 · The paper itself

Abstract

With an overall survival rate of 2-9% at 5 years, pancreatic ductal adenocarcinoma (PDAC) is currently the fourth leading cause of cancer-related deaths in the industrialized world and is predicted to become the second by 2030. Owing to often late diagnosis and rare actionable molecular alterations, PDAC has not yet benefited from the recent therapeutic advances that immune checkpoint inhibitors (ICI) have provided in other cancer types, except in specific subgroups of patients presenting with tumors with high mutational burden (TMB) or microsatellite instability (MSI). The tumor microenvironment (TME) plays a substantial role in therapeutic resistance by facilitating immune evasion. An extracellular stromal protein, βig-h3/TGFβi, is involved in the pathogenesis of PDAC by hampering T cell activation and promoting stiffness of the TME. The study BIGHPANC included 41 patients with metastatic PDAC, and analyzed βig-h3 levels in serum and tumor samples to assess the βig-h3 prognostic value. βig-h3 serum levels are significantly associated with overall survival (HR 2.05, 95%CI 1.07-3.93;

Indexed as

BIGHPANCimmune checkpoint inhibitorspancreatic adenocarcinomapancreatic cancerprognostic analysisTGFbeta

Identifiers

PMID35455739
PMCPMC9025577
OpenAlexW4223475543

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.