Very low expression of PD-L1 in medullary thyroid carcinoma.

Détails

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Etat: Public
Version: Final published version
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ID Serval
serval:BIB_8220EE9B4DFA
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Very low expression of PD-L1 in medullary thyroid carcinoma.
Périodique
Endocrine-related cancer
Auteur⸱e⸱s
Bongiovanni M., Rebecchini C., Saglietti C., Bulliard J.L., Marino L., de Leval L., Sykiotis G.P.
ISSN
1479-6821 (Electronic)
ISSN-L
1351-0088
Statut éditorial
Publié
Date de publication
06/2017
Peer-reviewed
Oui
Volume
24
Numéro
6
Pages
L35-L38
Langue
anglais
Notes
Publication types: Letter ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
Monoclonal antibodies that inhibit the interaction between PD1 and PD-L1 are approved for clinical use in several cancer types, and they are also in clinical trials for additional indications, including thyroid carcinomas. A few papers have reported on PD-L1 expression in thyroid carcinomas, including a recent large study by Ahn et al. in Endocrine-Related Cancer using tissue microarrays on differentiated and anaplastic thyroid carcinoma. However, the expression of PD-L1 in medullary thyroid carcinoma (MTC) has not been reported so far, even though ongoing clinical studies aim to test the effectiveness of checkpoint inhibitors in this rare histotype as well. We thus assessed PD-L1 expression in both tumor cells and tumor-infiltrating immune cells in a series of 16 MTC cases at a tertiary center. Tumor cells were positive in only one case, which had 5% positive cells. 1% and 2% of the inflammatory cells were stained in two cases. No correlation was evident between PD-L1 expression and survival in our series. Our results are indicative of near uniform absence of PD-L1 expression in MTC and its accompanying inflammatory cells; these results should be replicated on a larger scale in other centers. Definitive answers regarding the utility of PD1/PD-L1 immunophenotyping in MTC and of the use of checkpoint inhibitors in the treatment of this aggressive and rare thyroid cancer are expected from ongoing clinical trials, which should perform correlations with PD1/PD-L1 expression.
Mots-clé
Adult, Aged, B7-H1 Antigen/antagonists & inhibitors, B7-H1 Antigen/biosynthesis, B7-H1 Antigen/immunology, Carcinoma, Neuroendocrine/immunology, Carcinoma, Neuroendocrine/metabolism, Carcinoma, Neuroendocrine/pathology, Carcinoma, Neuroendocrine/therapy, Female, Humans, Immunotherapy, Male, Middle Aged, Thyroid Neoplasms/immunology, Thyroid Neoplasms/metabolism, Thyroid Neoplasms/pathology, Thyroid Neoplasms/therapy
Pubmed
Web of science
Open Access
Oui
Création de la notice
20/04/2017 14:00
Dernière modification de la notice
21/11/2022 9:28
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