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When to apply immune checkpoint inhibitor in patients with refractory advanced gastric cancer

Background: Immune checkpoint inhibitors (ICIs) show clinical benefit in patients with refractory advanced gastric cancer (GC). The ICIs in routine clinical practice have been used in various treatment lines. Therefore, we investigated the timing for application of ICI in patients with refractory ad...

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Autores principales: Kim, Hongsik, Kim, Hana, Lee, Minsang, Kwon, Minsuk, Hong, Jung Yong, Lee, Jeeyun, Lim, Ho Yeong, Kang, Won Ki, Kim, Seung Tae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8364657/
https://www.ncbi.nlm.nih.gov/pubmed/34405028
http://dx.doi.org/10.7150/jca.62853
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author Kim, Hongsik
Kim, Hana
Lee, Minsang
Kwon, Minsuk
Hong, Jung Yong
Lee, Jeeyun
Lim, Ho Yeong
Kang, Won Ki
Kim, Seung Tae
author_facet Kim, Hongsik
Kim, Hana
Lee, Minsang
Kwon, Minsuk
Hong, Jung Yong
Lee, Jeeyun
Lim, Ho Yeong
Kang, Won Ki
Kim, Seung Tae
author_sort Kim, Hongsik
collection PubMed
description Background: Immune checkpoint inhibitors (ICIs) show clinical benefit in patients with refractory advanced gastric cancer (GC). The ICIs in routine clinical practice have been used in various treatment lines. Therefore, we investigated the timing for application of ICI in patients with refractory advanced GC. Methods: We analyzed 187 patients with refractory advanced or recurrent GC who received ICIS as a 3rd- or 4th-line treatment between September 2015 and October 2020. Clinical outcomes of overall survival (OS), progression-free survival (PFS), objective response rate (ORR), and disease control rate (DCR) were evaluated. Results: Among 187 patients, 105 received ICIs as a 3rd-line treatment and 82 as a 4th line. The ORR for ICIs was 10.5% (11/105) in 3rd line and 8.5% (7/82) in 4th line. The DCR for ICIs was 36.2% (38/105) in 3rd-line treatment and 31.7% (26/82) in 4th line. There was no significant difference for ORR (P = 0.819) or DCR (P = 0.870). The median PFS and OS to ICIs was 1.4 months (95% CI, 1.1 to 1.8 months) and 4.4 months (95% CI, 1.6 to 7.2 months) in 3rd line and 1.8 months (95% CI, 1.4 to 2.3 months) and 2.8 months (95% CI, 2.2 to 3.4 months) in 4th line. The median PFS and OS to ICIs was not different between 3rd line and 4th line (P = 0.495 and P=0.208, respectively). There were also no significant difference for PFS and OS between PD-L1-positive tumors (CPS≥1) and PD-L1-negative tumors (P = 0.910 and P=0.931, respectively). Conclusions: ICIs showed similar clinical benefits in the 3rd-line and 4th-line settings. ICIs might be a reasonable approach for patients with refractory GC in the setting of 3rd-line or 4th-line treatment options.
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spelling pubmed-83646572021-08-16 When to apply immune checkpoint inhibitor in patients with refractory advanced gastric cancer Kim, Hongsik Kim, Hana Lee, Minsang Kwon, Minsuk Hong, Jung Yong Lee, Jeeyun Lim, Ho Yeong Kang, Won Ki Kim, Seung Tae J Cancer Research Paper Background: Immune checkpoint inhibitors (ICIs) show clinical benefit in patients with refractory advanced gastric cancer (GC). The ICIs in routine clinical practice have been used in various treatment lines. Therefore, we investigated the timing for application of ICI in patients with refractory advanced GC. Methods: We analyzed 187 patients with refractory advanced or recurrent GC who received ICIS as a 3rd- or 4th-line treatment between September 2015 and October 2020. Clinical outcomes of overall survival (OS), progression-free survival (PFS), objective response rate (ORR), and disease control rate (DCR) were evaluated. Results: Among 187 patients, 105 received ICIs as a 3rd-line treatment and 82 as a 4th line. The ORR for ICIs was 10.5% (11/105) in 3rd line and 8.5% (7/82) in 4th line. The DCR for ICIs was 36.2% (38/105) in 3rd-line treatment and 31.7% (26/82) in 4th line. There was no significant difference for ORR (P = 0.819) or DCR (P = 0.870). The median PFS and OS to ICIs was 1.4 months (95% CI, 1.1 to 1.8 months) and 4.4 months (95% CI, 1.6 to 7.2 months) in 3rd line and 1.8 months (95% CI, 1.4 to 2.3 months) and 2.8 months (95% CI, 2.2 to 3.4 months) in 4th line. The median PFS and OS to ICIs was not different between 3rd line and 4th line (P = 0.495 and P=0.208, respectively). There were also no significant difference for PFS and OS between PD-L1-positive tumors (CPS≥1) and PD-L1-negative tumors (P = 0.910 and P=0.931, respectively). Conclusions: ICIs showed similar clinical benefits in the 3rd-line and 4th-line settings. ICIs might be a reasonable approach for patients with refractory GC in the setting of 3rd-line or 4th-line treatment options. Ivyspring International Publisher 2021-07-25 /pmc/articles/PMC8364657/ /pubmed/34405028 http://dx.doi.org/10.7150/jca.62853 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Kim, Hongsik
Kim, Hana
Lee, Minsang
Kwon, Minsuk
Hong, Jung Yong
Lee, Jeeyun
Lim, Ho Yeong
Kang, Won Ki
Kim, Seung Tae
When to apply immune checkpoint inhibitor in patients with refractory advanced gastric cancer
title When to apply immune checkpoint inhibitor in patients with refractory advanced gastric cancer
title_full When to apply immune checkpoint inhibitor in patients with refractory advanced gastric cancer
title_fullStr When to apply immune checkpoint inhibitor in patients with refractory advanced gastric cancer
title_full_unstemmed When to apply immune checkpoint inhibitor in patients with refractory advanced gastric cancer
title_short When to apply immune checkpoint inhibitor in patients with refractory advanced gastric cancer
title_sort when to apply immune checkpoint inhibitor in patients with refractory advanced gastric cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8364657/
https://www.ncbi.nlm.nih.gov/pubmed/34405028
http://dx.doi.org/10.7150/jca.62853
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