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Relationship between immune‐related adverse events and treatment effectiveness in extensive disease small cell lung cancer
BACKGROUND: This study aimed to assess the relationship between immune response adverse events (irAEs) and treatment efficacy in patients with extensive disease small cell lung cancer (ED‐SCLC). METHODS: We retrospectively evaluated the clinical effects in 40 ED‐SCLC patients who had received immune...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423651/ https://www.ncbi.nlm.nih.gov/pubmed/37365145 http://dx.doi.org/10.1111/1759-7714.15010 |
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author | Yokoo, Keiki Kitamura, Yauo Suzuki, Keito Morikawa, Kohei Sawai, Takeo Honda, Hiroyuki Kudo, Sayaka Yamada, Gen |
author_facet | Yokoo, Keiki Kitamura, Yauo Suzuki, Keito Morikawa, Kohei Sawai, Takeo Honda, Hiroyuki Kudo, Sayaka Yamada, Gen |
author_sort | Yokoo, Keiki |
collection | PubMed |
description | BACKGROUND: This study aimed to assess the relationship between immune response adverse events (irAEs) and treatment efficacy in patients with extensive disease small cell lung cancer (ED‐SCLC). METHODS: We retrospectively evaluated the clinical effects in 40 ED‐SCLC patients who had received immune‐checkpoint inhibitors (ICIs), platinum agents, and etoposide between September 2019 and September 2021. We identified and compared patients belonging to two groups: irAE and non‐irAE. RESULTS: Fifteen patients experienced irAEs, and 25 did not. The median progression‐free survival in patients with irAE was longer than that in patients without irAE (12.6 months [95% CI: 6.3–19.3 months] vs. 7.2 months [95% CI: 5.8–7.9 months], p = 0.0108). However, the median overall survival (OS) was similar between irAE and non‐irAE groups (27.6 months [95% CI: 15.4–NA] vs. 24.9 months [95% CI: 13.7–NA], p = 0.268). Seven (46.7%) in the irAE group and 20 (80%) in the non‐irAE group received sequential therapy. The median OS was prolonged in patients who received first‐ and second‐line therapy than in those who received first‐line therapy alone (27.6 months [95% CI: 19.2–NA] vs. 6.6 months [95% CI: 0.3–NA], p = 0.053). Grade ≧ 3 irAEs occurred in five (12.5%) patients. Among them, grade 5 irAEs were observed in two patients, including exacerbation of polymyositis and pulmonary arterial embolism. CONCLUSION: In this study, the development of irAEs did not affect OS in patients with ED‐SCLC who received platinum‐based agents, etoposide, or ICI therapy. We determined that managing irAEs and administering first‐ and second‐line therapies could contribute to prolonged OS. |
format | Online Article Text |
id | pubmed-10423651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-104236512023-08-15 Relationship between immune‐related adverse events and treatment effectiveness in extensive disease small cell lung cancer Yokoo, Keiki Kitamura, Yauo Suzuki, Keito Morikawa, Kohei Sawai, Takeo Honda, Hiroyuki Kudo, Sayaka Yamada, Gen Thorac Cancer Original Articles BACKGROUND: This study aimed to assess the relationship between immune response adverse events (irAEs) and treatment efficacy in patients with extensive disease small cell lung cancer (ED‐SCLC). METHODS: We retrospectively evaluated the clinical effects in 40 ED‐SCLC patients who had received immune‐checkpoint inhibitors (ICIs), platinum agents, and etoposide between September 2019 and September 2021. We identified and compared patients belonging to two groups: irAE and non‐irAE. RESULTS: Fifteen patients experienced irAEs, and 25 did not. The median progression‐free survival in patients with irAE was longer than that in patients without irAE (12.6 months [95% CI: 6.3–19.3 months] vs. 7.2 months [95% CI: 5.8–7.9 months], p = 0.0108). However, the median overall survival (OS) was similar between irAE and non‐irAE groups (27.6 months [95% CI: 15.4–NA] vs. 24.9 months [95% CI: 13.7–NA], p = 0.268). Seven (46.7%) in the irAE group and 20 (80%) in the non‐irAE group received sequential therapy. The median OS was prolonged in patients who received first‐ and second‐line therapy than in those who received first‐line therapy alone (27.6 months [95% CI: 19.2–NA] vs. 6.6 months [95% CI: 0.3–NA], p = 0.053). Grade ≧ 3 irAEs occurred in five (12.5%) patients. Among them, grade 5 irAEs were observed in two patients, including exacerbation of polymyositis and pulmonary arterial embolism. CONCLUSION: In this study, the development of irAEs did not affect OS in patients with ED‐SCLC who received platinum‐based agents, etoposide, or ICI therapy. We determined that managing irAEs and administering first‐ and second‐line therapies could contribute to prolonged OS. John Wiley & Sons Australia, Ltd 2023-06-26 /pmc/articles/PMC10423651/ /pubmed/37365145 http://dx.doi.org/10.1111/1759-7714.15010 Text en © 2023 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Yokoo, Keiki Kitamura, Yauo Suzuki, Keito Morikawa, Kohei Sawai, Takeo Honda, Hiroyuki Kudo, Sayaka Yamada, Gen Relationship between immune‐related adverse events and treatment effectiveness in extensive disease small cell lung cancer |
title | Relationship between immune‐related adverse events and treatment effectiveness in extensive disease small cell lung cancer |
title_full | Relationship between immune‐related adverse events and treatment effectiveness in extensive disease small cell lung cancer |
title_fullStr | Relationship between immune‐related adverse events and treatment effectiveness in extensive disease small cell lung cancer |
title_full_unstemmed | Relationship between immune‐related adverse events and treatment effectiveness in extensive disease small cell lung cancer |
title_short | Relationship between immune‐related adverse events and treatment effectiveness in extensive disease small cell lung cancer |
title_sort | relationship between immune‐related adverse events and treatment effectiveness in extensive disease small cell lung cancer |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423651/ https://www.ncbi.nlm.nih.gov/pubmed/37365145 http://dx.doi.org/10.1111/1759-7714.15010 |
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