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PD-1 inhibitor combined with apatinib for advanced gastric or esophagogastric junction cancer: a retrospective study

BACKGROUND: Nivolumab and pembrolizumab were approved as immune checkpoint inhibitors for third-line treatment of advanced gastric or esophagogastric junction cancer (GC/EGJC) in 2017. However, immunotherapy monotherapy has low efficacy. Apatinib has been proven effective in advanced GC/EGJC. Numero...

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Autores principales: Wei, Qing, Yuan, Xing, Li, Jingjing, Xu, Qi, Ying, Jieer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798944/
https://www.ncbi.nlm.nih.gov/pubmed/35117897
http://dx.doi.org/10.21037/tcr-20-1333
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author Wei, Qing
Yuan, Xing
Li, Jingjing
Xu, Qi
Ying, Jieer
author_facet Wei, Qing
Yuan, Xing
Li, Jingjing
Xu, Qi
Ying, Jieer
author_sort Wei, Qing
collection PubMed
description BACKGROUND: Nivolumab and pembrolizumab were approved as immune checkpoint inhibitors for third-line treatment of advanced gastric or esophagogastric junction cancer (GC/EGJC) in 2017. However, immunotherapy monotherapy has low efficacy. Apatinib has been proven effective in advanced GC/EGJC. Numerous studies have shown that immunotherapy has a synergistic effect when combined with targeted drug therapy. Based on these facts and to assess the efficacy and safety of programmed death 1 (PD-1) inhibitor and apatinib as combination therapy in patients (pts) with unresectable locally advanced or metastatic GC/EGJC, a retrospective clinical research study was carried out. METHODS: Pts (n=24) received PD-1 inhibitor and apatinib (250 mg once daily) as second- or third-line therapy in this observational, retrospective study. The primary objectives were efficacy and safety. RESULTS: At data cut-off (December 31, 2019), 24 pts were enrolled. Of the 19 pts who were evaluable, the objective response rate (ORR) was 26.3% (5/19), the median progression-free survival (PFS) was 3.0 (95% CI: 1.3 to 4.7) months, and the median overall survival (OS) was not reached. Grade 3 or 4 treatment-related adverse events (TRAEs) occurred in 3 (15.8%) of the 19 pts. These adverse events (AEs) included pruritus, rash, hand-foot syndrome, and increased aspartate aminotransferase (AST) or alanine aminotransferase (ALT). No treatment-related deaths occurred. CONCLUSIONS: Combination therapy of PD-1 inhibitor and apatinib showed encouraging clinical activity and demonstrated tolerable toxicity in pts with advanced GC/EGJC. Hence, our work provide rationale for the combination of PD-1 inhibitor and apatinib in advanced GC/EGJC.
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spelling pubmed-87989442022-02-02 PD-1 inhibitor combined with apatinib for advanced gastric or esophagogastric junction cancer: a retrospective study Wei, Qing Yuan, Xing Li, Jingjing Xu, Qi Ying, Jieer Transl Cancer Res Original Article BACKGROUND: Nivolumab and pembrolizumab were approved as immune checkpoint inhibitors for third-line treatment of advanced gastric or esophagogastric junction cancer (GC/EGJC) in 2017. However, immunotherapy monotherapy has low efficacy. Apatinib has been proven effective in advanced GC/EGJC. Numerous studies have shown that immunotherapy has a synergistic effect when combined with targeted drug therapy. Based on these facts and to assess the efficacy and safety of programmed death 1 (PD-1) inhibitor and apatinib as combination therapy in patients (pts) with unresectable locally advanced or metastatic GC/EGJC, a retrospective clinical research study was carried out. METHODS: Pts (n=24) received PD-1 inhibitor and apatinib (250 mg once daily) as second- or third-line therapy in this observational, retrospective study. The primary objectives were efficacy and safety. RESULTS: At data cut-off (December 31, 2019), 24 pts were enrolled. Of the 19 pts who were evaluable, the objective response rate (ORR) was 26.3% (5/19), the median progression-free survival (PFS) was 3.0 (95% CI: 1.3 to 4.7) months, and the median overall survival (OS) was not reached. Grade 3 or 4 treatment-related adverse events (TRAEs) occurred in 3 (15.8%) of the 19 pts. These adverse events (AEs) included pruritus, rash, hand-foot syndrome, and increased aspartate aminotransferase (AST) or alanine aminotransferase (ALT). No treatment-related deaths occurred. CONCLUSIONS: Combination therapy of PD-1 inhibitor and apatinib showed encouraging clinical activity and demonstrated tolerable toxicity in pts with advanced GC/EGJC. Hence, our work provide rationale for the combination of PD-1 inhibitor and apatinib in advanced GC/EGJC. AME Publishing Company 2020-09 /pmc/articles/PMC8798944/ /pubmed/35117897 http://dx.doi.org/10.21037/tcr-20-1333 Text en 2020 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Original Article
Wei, Qing
Yuan, Xing
Li, Jingjing
Xu, Qi
Ying, Jieer
PD-1 inhibitor combined with apatinib for advanced gastric or esophagogastric junction cancer: a retrospective study
title PD-1 inhibitor combined with apatinib for advanced gastric or esophagogastric junction cancer: a retrospective study
title_full PD-1 inhibitor combined with apatinib for advanced gastric or esophagogastric junction cancer: a retrospective study
title_fullStr PD-1 inhibitor combined with apatinib for advanced gastric or esophagogastric junction cancer: a retrospective study
title_full_unstemmed PD-1 inhibitor combined with apatinib for advanced gastric or esophagogastric junction cancer: a retrospective study
title_short PD-1 inhibitor combined with apatinib for advanced gastric or esophagogastric junction cancer: a retrospective study
title_sort pd-1 inhibitor combined with apatinib for advanced gastric or esophagogastric junction cancer: a retrospective study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798944/
https://www.ncbi.nlm.nih.gov/pubmed/35117897
http://dx.doi.org/10.21037/tcr-20-1333
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