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Clinical outcomes of immune checkpoint inhibitor therapy for advanced lung adenosquamous carcinoma

BACKGROUND: Primary adenosquamous carcinoma (ASC) of the lung is a rare and aggressive disease and limited information is available on the efficacy of immune checkpoint inhibitors (ICIs) for this disease. Here, we evaluated the expression status of programmed death-1 ligand 1 (PD-L1) and efficacy of...

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Autores principales: Wei, Jingwen, Xiang, Jing, Hao, Yue, Si, Jinfei, Gu, Xiaodong, Xu, Manyi, Song, Zhengbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9992578/
https://www.ncbi.nlm.nih.gov/pubmed/36910045
http://dx.doi.org/10.21037/jtd-22-1011
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author Wei, Jingwen
Xiang, Jing
Hao, Yue
Si, Jinfei
Gu, Xiaodong
Xu, Manyi
Song, Zhengbo
author_facet Wei, Jingwen
Xiang, Jing
Hao, Yue
Si, Jinfei
Gu, Xiaodong
Xu, Manyi
Song, Zhengbo
author_sort Wei, Jingwen
collection PubMed
description BACKGROUND: Primary adenosquamous carcinoma (ASC) of the lung is a rare and aggressive disease and limited information is available on the efficacy of immune checkpoint inhibitors (ICIs) for this disease. Here, we evaluated the expression status of programmed death-1 ligand 1 (PD-L1) and efficacy of ICIs in patients with pulmonary ASC. METHODS: The efficacy and toxicity of ICIs were examined in 38 patients with previously treated lung ASC from November 2017 to October 2021 in Zhejiang Cancer Hospital (Hangzhou, China). Survival curves were plotted using the Kaplan-Meier method and the Cox proportional hazards model applied for univariate and multivariate analyses. RESULTS: A total of 38 patients with ASC were included in this retrospective study. ICI treatment induced an objective response rate (ORR) of 23.7% and a disease control rate (DCR) of 86.8%. The median progression-free survival (PFS) and median overall survival (OS) were 5.47 and 24.10 months, respectively. Seventeen patients were successfully evaluated for PD-L1 expression status, with 11 (64.7%) identified as PD-L1-positive. ORR and DCR for PD-L1-positive patients were 36.4% (4/11) and 100% (11/11) and the corresponding values for PD-L1-negative patients were 0 (0/6) and 50% (3/6), respectively. The median PFS of PD-L1-positive and PD-L1-negative patient groups was 5.00 and 1.90 months (P=0.166) while the median OS was 11.30 months and not reached, respectively (P=0.966). The incidence rate of immune-related adverse events (irAEs) was 52.6%, with 13.2% grade 3−4 irAEs. The most common irAEs were malaise and pneumonitis. One patient died of pneumonitis during the study. CONCLUSIONS: ICIs show considerable potential as a treatment option for lung ASC. PFS and OS rates are similar for PD-L1-positive and PD-L1-negative patients. Further large-scale studies are required to establish the relationship between PD-L1 expression and response to ICIs in ASC.
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spelling pubmed-99925782023-03-09 Clinical outcomes of immune checkpoint inhibitor therapy for advanced lung adenosquamous carcinoma Wei, Jingwen Xiang, Jing Hao, Yue Si, Jinfei Gu, Xiaodong Xu, Manyi Song, Zhengbo J Thorac Dis Original Article BACKGROUND: Primary adenosquamous carcinoma (ASC) of the lung is a rare and aggressive disease and limited information is available on the efficacy of immune checkpoint inhibitors (ICIs) for this disease. Here, we evaluated the expression status of programmed death-1 ligand 1 (PD-L1) and efficacy of ICIs in patients with pulmonary ASC. METHODS: The efficacy and toxicity of ICIs were examined in 38 patients with previously treated lung ASC from November 2017 to October 2021 in Zhejiang Cancer Hospital (Hangzhou, China). Survival curves were plotted using the Kaplan-Meier method and the Cox proportional hazards model applied for univariate and multivariate analyses. RESULTS: A total of 38 patients with ASC were included in this retrospective study. ICI treatment induced an objective response rate (ORR) of 23.7% and a disease control rate (DCR) of 86.8%. The median progression-free survival (PFS) and median overall survival (OS) were 5.47 and 24.10 months, respectively. Seventeen patients were successfully evaluated for PD-L1 expression status, with 11 (64.7%) identified as PD-L1-positive. ORR and DCR for PD-L1-positive patients were 36.4% (4/11) and 100% (11/11) and the corresponding values for PD-L1-negative patients were 0 (0/6) and 50% (3/6), respectively. The median PFS of PD-L1-positive and PD-L1-negative patient groups was 5.00 and 1.90 months (P=0.166) while the median OS was 11.30 months and not reached, respectively (P=0.966). The incidence rate of immune-related adverse events (irAEs) was 52.6%, with 13.2% grade 3−4 irAEs. The most common irAEs were malaise and pneumonitis. One patient died of pneumonitis during the study. CONCLUSIONS: ICIs show considerable potential as a treatment option for lung ASC. PFS and OS rates are similar for PD-L1-positive and PD-L1-negative patients. Further large-scale studies are required to establish the relationship between PD-L1 expression and response to ICIs in ASC. AME Publishing Company 2023-01-09 2023-02-28 /pmc/articles/PMC9992578/ /pubmed/36910045 http://dx.doi.org/10.21037/jtd-22-1011 Text en 2023 Journal of Thoracic Disease. 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 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Wei, Jingwen
Xiang, Jing
Hao, Yue
Si, Jinfei
Gu, Xiaodong
Xu, Manyi
Song, Zhengbo
Clinical outcomes of immune checkpoint inhibitor therapy for advanced lung adenosquamous carcinoma
title Clinical outcomes of immune checkpoint inhibitor therapy for advanced lung adenosquamous carcinoma
title_full Clinical outcomes of immune checkpoint inhibitor therapy for advanced lung adenosquamous carcinoma
title_fullStr Clinical outcomes of immune checkpoint inhibitor therapy for advanced lung adenosquamous carcinoma
title_full_unstemmed Clinical outcomes of immune checkpoint inhibitor therapy for advanced lung adenosquamous carcinoma
title_short Clinical outcomes of immune checkpoint inhibitor therapy for advanced lung adenosquamous carcinoma
title_sort clinical outcomes of immune checkpoint inhibitor therapy for advanced lung adenosquamous carcinoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9992578/
https://www.ncbi.nlm.nih.gov/pubmed/36910045
http://dx.doi.org/10.21037/jtd-22-1011
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