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

adrenocortical carcinoma p53 prognostic tissue-micro-array

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
29 Apr 2022
Historique:
received: 16 03 2022
revised: 13 04 2022
accepted: 20 04 2022
entrez: 14 5 2022
pubmed: 15 5 2022
medline: 15 5 2022
Statut: epublish

Résumé

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.

Identifiants

pubmed: 35565353
pii: cancers14092225
doi: 10.3390/cancers14092225
pmc: PMC9099575
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : HRA Pharma (France)
ID : x
Organisme : association surrenales
ID : x

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Auteurs

Segolene Hescot (S)

Department of Nuclear Medicine, Institut Curie, 92210 Saint Cloud, France.

Matthieu Faron (M)

Department of Surgery, Gustave Roussy, 94805 Villejuif, France.

Manal Kordahi (M)

Department of Pathology, Gustave Roussy, 94805 Villejuif, France.

Christine Do Cao (C)

Department of Endocrinology, Centre Hospitalier Universitaire Lille, 59000 Lille, France.

Annabelle Naman (A)

Department of Endocrine Oncology, Gustave Roussy, 94805 Villejuif, France.

Livia Lamartina (L)

Department of Endocrine Oncology, Gustave Roussy, 94805 Villejuif, France.

Julien Hadoux (J)

Department of Endocrine Oncology, Gustave Roussy, 94805 Villejuif, France.

Sophie Leboulleux (S)

Department of Endocrine Oncology, Gustave Roussy, 94805 Villejuif, France.

Francois Pattou (F)

Department of General and Endocrine Surgery, Centre Hospitalier Universitaire Lille, Université de Lille, 59000 Lille, France.

Sébastien Aubert (S)

Institut of Pathology, Centre Hospitalier Universitaire Lille, 59000 Lille, France.

Jean-Yves Scoazec (JY)

Department of Pathology, Gustave Roussy, 94805 Villejuif, France.

Abir Al Ghuzlan (A)

Department of Pathology, Gustave Roussy, 94805 Villejuif, France.

Eric Baudin (E)

Department of Endocrine Oncology, Gustave Roussy, 94805 Villejuif, France.

Classifications MeSH