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Efficacy and safety of immune checkpoint inhibitors in lung large-cell neuroendocrine carcinoma
BACKGROUND: Lung large-cell neuroendocrine carcinoma (L-LCNEC) is a rare and highly aggressive neuroendocrine tumor. There is currently no standard therapeutic regimen, and systemic chemotherapy results in poor prognosis. Due to the rarity of L-LCNEC, the efficacy and safety of immune checkpoint inh...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10482626/ https://www.ncbi.nlm.nih.gov/pubmed/37691658 http://dx.doi.org/10.21037/jtd-23-348 |
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author | Shi, Zheng Wei, Jingwen Xu, Manyi Song, Zhengbo |
author_facet | Shi, Zheng Wei, Jingwen Xu, Manyi Song, Zhengbo |
author_sort | Shi, Zheng |
collection | PubMed |
description | BACKGROUND: Lung large-cell neuroendocrine carcinoma (L-LCNEC) is a rare and highly aggressive neuroendocrine tumor. There is currently no standard therapeutic regimen, and systemic chemotherapy results in poor prognosis. Due to the rarity of L-LCNEC, the efficacy and safety of immune checkpoint inhibitors (ICIs) remain unclear. METHODS: This study included 34 L-LCNEC patients administered ICIs at Zhejiang Cancer Hospital, from February 6, 2018 to February 6, 2023. The treatment responses were evaluated. Fisher’s exact test was used to compare categorical variables, and the Kaplan-Meier method was used for survival analyses. Cox regression was used for multivariate analysis. RESULTS: The objective response rate (ORR) of 34 patients was 29.4%, the disease control rate (DCR) was 82.4%, the median progression-free survival (PFS) was 6.30 months, and the median overall survival (OS) was 14.77 months. The ORRs of combined LCNEC (n=7) and pure LCNEC (n=27) were 14.3% and 33.3%; the DCRs were 100% and 77.8%; the median PFSs were 12.48 and 5.6 months (P=0.032); and the median OSs were 21.27 and 14.73 months, respectively (P=0.233). The observed incidence of immune-related adverse events (irAEs) was 61.8%, primarily occurring in grades 1/2 (58.8%) and grade 3 (5.9%). Elevated aminotransferases (14.7%), pneumonia (8.8%), and fatigue (8.8%) were the most common irAEs. CONCLUSIONS: ICIs treatment showed efficacy and safety in advanced L-LCNEC, with the potential for greater benefits in the combined LCNEC subtype. |
format | Online Article Text |
id | pubmed-10482626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-104826262023-09-08 Efficacy and safety of immune checkpoint inhibitors in lung large-cell neuroendocrine carcinoma Shi, Zheng Wei, Jingwen Xu, Manyi Song, Zhengbo J Thorac Dis Original Article BACKGROUND: Lung large-cell neuroendocrine carcinoma (L-LCNEC) is a rare and highly aggressive neuroendocrine tumor. There is currently no standard therapeutic regimen, and systemic chemotherapy results in poor prognosis. Due to the rarity of L-LCNEC, the efficacy and safety of immune checkpoint inhibitors (ICIs) remain unclear. METHODS: This study included 34 L-LCNEC patients administered ICIs at Zhejiang Cancer Hospital, from February 6, 2018 to February 6, 2023. The treatment responses were evaluated. Fisher’s exact test was used to compare categorical variables, and the Kaplan-Meier method was used for survival analyses. Cox regression was used for multivariate analysis. RESULTS: The objective response rate (ORR) of 34 patients was 29.4%, the disease control rate (DCR) was 82.4%, the median progression-free survival (PFS) was 6.30 months, and the median overall survival (OS) was 14.77 months. The ORRs of combined LCNEC (n=7) and pure LCNEC (n=27) were 14.3% and 33.3%; the DCRs were 100% and 77.8%; the median PFSs were 12.48 and 5.6 months (P=0.032); and the median OSs were 21.27 and 14.73 months, respectively (P=0.233). The observed incidence of immune-related adverse events (irAEs) was 61.8%, primarily occurring in grades 1/2 (58.8%) and grade 3 (5.9%). Elevated aminotransferases (14.7%), pneumonia (8.8%), and fatigue (8.8%) were the most common irAEs. CONCLUSIONS: ICIs treatment showed efficacy and safety in advanced L-LCNEC, with the potential for greater benefits in the combined LCNEC subtype. AME Publishing Company 2023-07-24 2023-08-31 /pmc/articles/PMC10482626/ /pubmed/37691658 http://dx.doi.org/10.21037/jtd-23-348 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 Shi, Zheng Wei, Jingwen Xu, Manyi Song, Zhengbo Efficacy and safety of immune checkpoint inhibitors in lung large-cell neuroendocrine carcinoma |
title | Efficacy and safety of immune checkpoint inhibitors in lung large-cell neuroendocrine carcinoma |
title_full | Efficacy and safety of immune checkpoint inhibitors in lung large-cell neuroendocrine carcinoma |
title_fullStr | Efficacy and safety of immune checkpoint inhibitors in lung large-cell neuroendocrine carcinoma |
title_full_unstemmed | Efficacy and safety of immune checkpoint inhibitors in lung large-cell neuroendocrine carcinoma |
title_short | Efficacy and safety of immune checkpoint inhibitors in lung large-cell neuroendocrine carcinoma |
title_sort | efficacy and safety of immune checkpoint inhibitors in lung large-cell neuroendocrine carcinoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10482626/ https://www.ncbi.nlm.nih.gov/pubmed/37691658 http://dx.doi.org/10.21037/jtd-23-348 |
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