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IMMUNOTHERAPY TREATMENT AGAINST CERVICAL CANCER

Authors :
Guadalupe E Trejo-Durán
Lucely Cetina-Pérez
Elva G Vanoye-Carlo
Leonardo S Lino-Silva
Cristina Alvarado-Silva
Tatiana Galicia-Carmona
Roberto Jiménez-Lima
Omar H Castañeda-Renderos
Eder Arango-Bravo
Celia Flores-de la Torre
Alfonso Dueñas-González
Source :
Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion. 72(4)
Publication Year :
2020

Abstract

Cervical cancer (CC) is one of the most common gynecological tumors and an important health problem, especially in developing countries. The vast majority of patients in early stages are cured of the disease with surgical treatment and with concomitant chemoradiotherapy in locally advanced stages. However, in patients with recurrent, persistent, or metastatic cervical CC, the effectiveness of treatment is limited, except for the combination of chemotherapy based on platinum doublets plus bevacizumab, the treatment that has achieved the best results to date. Programmed cell death-1/PD ligand-1 (PD-1/PD-L1) inhibitors could be a novel and cutting-edge therapeutic option to improve clinical outcomes in this group of patients. Thus far, there are a few Phase I/II clinical trials that have assessed the usefulness of pembrolizumab and nivolumab in this group of patients; these include the KEYNOTE 028, KEYNOTE 158, and CHECKMATE 358 trials, in which clinical benefit has been proven with PD-1/PD-L1 inhibitors in recurrent, persistent, or metastatic CC, as second-line treatment. There are also some ongoing trials that could provide further evidence on the PD-1/PD-L1 pathway as a therapeutic target in CC. In this review, we will focus on the usefulness of these PD-1/PDL1 inhibitors in CC, as well as on trials that are still in the recruitment phase, to confirm their effectiveness in this clinical setting.

Details

ISSN :
00348376
Volume :
72
Issue :
4
Database :
OpenAIRE
Journal :
Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion
Accession number :
edsair.doi.dedup.....85dbf6326b8fc981c4f0b08400cf61e1