Evidence map›Paper›PMID 35565353›Full record

ArticleCancers2022

Screening for Prognostic Biomarkers in Metastatic Adrenocortical Carcinoma by Tissue Micro Arrays Analysis Identifies P53 as an Independent Prognostic Marker of Overall Survival.

Segolene Hescot, Matthieu Faron, Manal Kordahi, Christine Do Cao, Annabelle Naman, Livia Lamartina, Julien Hadoux, Sophie Leboulleux, Francois Pattou, Sébastien Aubert and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

13 authors at 5 institutions in 1 country.

Segolene HescotDepartment of Nuclear Medicine, Institut Curie, 92210 Saint Cloud, France.
Matthieu FaronDepartment of Surgery, Gustave Roussy, 94805 Villejuif, France.
Manal KordahiDepartment of Pathology, Gustave Roussy, 94805 Villejuif, France.
Christine Do CaoDepartment of Endocrinology, Centre Hospitalier Universitaire Lille, 59000 Lille, France.
Annabelle NamanDepartment of Endocrine Oncology, Gustave Roussy, 94805 Villejuif, France.
Livia LamartinaDepartment of Endocrine Oncology, Gustave Roussy, 94805 Villejuif, France.
Julien HadouxDepartment of Endocrine Oncology, Gustave Roussy, 94805 Villejuif, France.
Sophie LeboulleuxDepartment of Endocrine Oncology, Gustave Roussy, 94805 Villejuif, France.
Francois PattouDepartment of General and Endocrine Surgery, Centre Hospitalier Universitaire Lille, Université de Lille, 59000 Lille, France.ORCID 0000-0001-8388-3766
Sébastien AubertInstitut of Pathology, Centre Hospitalier Universitaire Lille, 59000 Lille, France.
Jean-Yves ScoazecDepartment of Pathology, Gustave Roussy, 94805 Villejuif, France.ORCID 0000-0003-1604-6823
Abir Al GhuzlanDepartment of Pathology, Gustave Roussy, 94805 Villejuif, France.
Eric BaudinDepartment of Endocrine Oncology, Gustave Roussy, 94805 Villejuif, France.
Institut Gustave Roussy · FRCentre Hospitalier Universitaire de Lille · FRCentre National de la Recherche Scientifique · FRInserm · FRInstitut Curie · FR

Funding

association surrenales xHRA Pharma (France) x
6 · The paper itself

Abstract

Advanced adrenocortical carcinoma (ACC) has poor but heterogeneous prognosis. Apart from Ki67 index, no prognostic or predictive biomarker has been validated in advanced ACC, so far. We aimed at analyzing expression of a large panel of proteins involved in known altered pathways in ACC (cell cycle, Wnt/ß-catenin, methylation) to identify and prioritize potential prognostic or predictive parameters metastatic ACC population. We conducted a retrospective multicentric study. Overall survival (OS) and partial response according to RECIST 1.1 were primary endpoints. TMA was set up and 16 markers were analyzed. Modified ENSAT and GRAS parameters were characterized for prognostic adjustment. Results: We included 66 patients with a mean age at metastatic diagnosis of 48.7 ± 15.5 years. Median survival was 27.8 months. After adjustment to mENSAT-GRAS parameters, p53 and PDxK were prognostic of OS. No potential biomarker has been identified as predictive factor of response. We identified for the first time P53 as an independent prognostic marker of metastatic adrenocortical carcinoma after mENSAT-GRAS parameter adjustment. Prognostic impact of Wnt/ß-catenin alterations was not confirmed in this cohort of metastatic ACC.

Indexed as

adrenocortical carcinomap53prognostictissue-micro-array

Identifiers

PMID35565353
PMCPMC9099575
OpenAlexW4225114470

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.