Cargando…

Targeted Treatment of Advanced Endometrial Cancer: Focus on Pembrolizumab

Endometrial cancer (EC) accounts for 2% of all new cancers. Advanced forms have a poor prognosis with barely 17% 5-year survival. The last few years improved our knowledge of EC with a new molecular classification derived from The Cancer Genome Atlas (TCGA). They are now divided between POLE mutant,...

Descripción completa

Detalles Bibliográficos
Autores principales: El-ghazzi, Nathan, Durando, Xavier, Giro, Alexia, Herrmann, Tressie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10243542/
https://www.ncbi.nlm.nih.gov/pubmed/37288137
http://dx.doi.org/10.2147/OTT.S368050
_version_ 1785054447443902464
author El-ghazzi, Nathan
Durando, Xavier
Giro, Alexia
Herrmann, Tressie
author_facet El-ghazzi, Nathan
Durando, Xavier
Giro, Alexia
Herrmann, Tressie
author_sort El-ghazzi, Nathan
collection PubMed
description Endometrial cancer (EC) accounts for 2% of all new cancers. Advanced forms have a poor prognosis with barely 17% 5-year survival. The last few years improved our knowledge of EC with a new molecular classification derived from The Cancer Genome Atlas (TCGA). They are now divided between POLE mutant, Microsatellite Instability High (MSI-H) or deficient in Mismatch Repair System (dMMR), TP53 mutant and no specific molecular profile. Until now, treatments for advanced EC have included conventional platinum-based chemotherapy or hormonotherapy. The revolution in oncology represented by the advent of immune checkpoints inhibitors (ICI) has also led to a major advance in the management of recurrent and metastatic EC. Pembrolizumab, a well-known anti PD-1, has firstly been approved as monotherapy in the second-line setting for dMMR/MSI-H advanced EC. More recently, a combination of lenvatinib with pembrolizumab offered a new effective option in the second line setting irrespectively of the MMR status, giving a new opportunity for these patients who had no actual standard of care before. This combination is currently being evaluated as frontline therapy. Despite exciting results, the main problem in identifying solid biomarkers remains unresolved and further investigations are required. New original combinations of pembrolizumab with other drugs including chemotherapy, poly ADPribose polymerase inhibitors (PARP-i) or tyrosine kinase inhibitors are being tested and promise exciting new therapeutic evolutions in a close future.
format Online
Article
Text
id pubmed-10243542
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Dove
record_format MEDLINE/PubMed
spelling pubmed-102435422023-06-07 Targeted Treatment of Advanced Endometrial Cancer: Focus on Pembrolizumab El-ghazzi, Nathan Durando, Xavier Giro, Alexia Herrmann, Tressie Onco Targets Ther Review Endometrial cancer (EC) accounts for 2% of all new cancers. Advanced forms have a poor prognosis with barely 17% 5-year survival. The last few years improved our knowledge of EC with a new molecular classification derived from The Cancer Genome Atlas (TCGA). They are now divided between POLE mutant, Microsatellite Instability High (MSI-H) or deficient in Mismatch Repair System (dMMR), TP53 mutant and no specific molecular profile. Until now, treatments for advanced EC have included conventional platinum-based chemotherapy or hormonotherapy. The revolution in oncology represented by the advent of immune checkpoints inhibitors (ICI) has also led to a major advance in the management of recurrent and metastatic EC. Pembrolizumab, a well-known anti PD-1, has firstly been approved as monotherapy in the second-line setting for dMMR/MSI-H advanced EC. More recently, a combination of lenvatinib with pembrolizumab offered a new effective option in the second line setting irrespectively of the MMR status, giving a new opportunity for these patients who had no actual standard of care before. This combination is currently being evaluated as frontline therapy. Despite exciting results, the main problem in identifying solid biomarkers remains unresolved and further investigations are required. New original combinations of pembrolizumab with other drugs including chemotherapy, poly ADPribose polymerase inhibitors (PARP-i) or tyrosine kinase inhibitors are being tested and promise exciting new therapeutic evolutions in a close future. Dove 2023-06-02 /pmc/articles/PMC10243542/ /pubmed/37288137 http://dx.doi.org/10.2147/OTT.S368050 Text en © 2023 El-ghazzi et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
El-ghazzi, Nathan
Durando, Xavier
Giro, Alexia
Herrmann, Tressie
Targeted Treatment of Advanced Endometrial Cancer: Focus on Pembrolizumab
title Targeted Treatment of Advanced Endometrial Cancer: Focus on Pembrolizumab
title_full Targeted Treatment of Advanced Endometrial Cancer: Focus on Pembrolizumab
title_fullStr Targeted Treatment of Advanced Endometrial Cancer: Focus on Pembrolizumab
title_full_unstemmed Targeted Treatment of Advanced Endometrial Cancer: Focus on Pembrolizumab
title_short Targeted Treatment of Advanced Endometrial Cancer: Focus on Pembrolizumab
title_sort targeted treatment of advanced endometrial cancer: focus on pembrolizumab
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10243542/
https://www.ncbi.nlm.nih.gov/pubmed/37288137
http://dx.doi.org/10.2147/OTT.S368050
work_keys_str_mv AT elghazzinathan targetedtreatmentofadvancedendometrialcancerfocusonpembrolizumab
AT durandoxavier targetedtreatmentofadvancedendometrialcancerfocusonpembrolizumab
AT giroalexia targetedtreatmentofadvancedendometrialcancerfocusonpembrolizumab
AT herrmanntressie targetedtreatmentofadvancedendometrialcancerfocusonpembrolizumab