Clear cell sarcoma: state-of-the art and perspectives.
Détails
ID Serval
serval:BIB_E565DF943C91
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Synthèse (review): revue aussi complète que possible des connaissances sur un sujet, rédigée à partir de l'analyse exhaustive des travaux publiés.
Collection
Publications
Institution
Titre
Clear cell sarcoma: state-of-the art and perspectives.
Périodique
Expert review of anticancer therapy
ISSN
1744-8328 (Electronic)
ISSN-L
1473-7140
Statut éditorial
Publié
Date de publication
03/2023
Peer-reviewed
Oui
Volume
23
Numéro
3
Pages
235-242
Langue
anglais
Notes
Publication types: Review ; Journal Article
Publication Status: ppublish
Publication Status: ppublish
Résumé
Clear cell sarcoma (CCS) is an ultrarare soft tissue sarcoma (STS) with a poor prognosis due to its propensity to metastasize and its low chemosensitivity. The standard treatment of localized CCS consists of wide surgical excision with or without additive radiotherapy. However, unresectable CCS is generally treated with conventional systemic therapies available for treatment of STS despite the weak scientific evidence to support its use.
In this review, we discuss the clinicopathologic characteristics of CSS, as well as the current treatment landscape and future therapeutic approaches.
The current treatment strategy of advanced CCSs, based on STSs regimens, shows a lack of effective options. Combination therapiesin particular, the association of immunotherapy and TKIs, represent a promising approach. Translational studies are needed in order to decipher the regulatory mechanisms involved in the oncogenesis of this ultrarare sarcoma and identify potential molecular targets.
In this review, we discuss the clinicopathologic characteristics of CSS, as well as the current treatment landscape and future therapeutic approaches.
The current treatment strategy of advanced CCSs, based on STSs regimens, shows a lack of effective options. Combination therapiesin particular, the association of immunotherapy and TKIs, represent a promising approach. Translational studies are needed in order to decipher the regulatory mechanisms involved in the oncogenesis of this ultrarare sarcoma and identify potential molecular targets.
Mots-clé
Humans, Sarcoma, Clear Cell/therapy, Immunotherapy, Soft Tissue Neoplasms/drug therapy, Clear cell sarcoma, chemotherapy resistance, immunotherapy, molecular targeted therapy
Pubmed
Web of science
Création de la notice
23/02/2023 13:41
Dernière modification de la notice
18/10/2023 6:11