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Prevalence of immune-related adverse events and anti-tumor efficacy following immune checkpoint inhibitor therapy in Japanese patients with various solid tumors

BACKGROUND: While immune checkpoint inhibitors (ICIs) occasionally cause immune-related adverse events (irAEs) in various organs, the prevalence of irAEs and potential risk factors have not been clarified. We identified irAE predictive factors and examined the relationship between the effect of ICIs...

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Autores principales: Yoshikawa, Yuki, Imamura, Michio, Yamauchi, Masami, Hayes, C. Nelson, Aikata, Hiroshi, Okamoto, Wataru, Miyata, Yoshihiro, Okada, Morihito, Hattori, Noboru, Sugiyama, Kazuhiko, Yoshioka, Yukio, Toratani, Shigeaki, Takechi, Masaaki, Ichinohe, Tatsuo, Ueda, Tsutomu, Takeno, Sachio, Kobayashi, Tsuyoshi, Ohdan, Hideki, Teishima, Jun, Hide, Michihiro, Nagata, Yasushi, Kudo, Yoshiki, Iida, Koji, Chayama, Kazuaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9706984/
https://www.ncbi.nlm.nih.gov/pubmed/36447159
http://dx.doi.org/10.1186/s12885-022-10327-7
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author Yoshikawa, Yuki
Imamura, Michio
Yamauchi, Masami
Hayes, C. Nelson
Aikata, Hiroshi
Okamoto, Wataru
Miyata, Yoshihiro
Okada, Morihito
Hattori, Noboru
Sugiyama, Kazuhiko
Yoshioka, Yukio
Toratani, Shigeaki
Takechi, Masaaki
Ichinohe, Tatsuo
Ueda, Tsutomu
Takeno, Sachio
Kobayashi, Tsuyoshi
Ohdan, Hideki
Teishima, Jun
Hide, Michihiro
Nagata, Yasushi
Kudo, Yoshiki
Iida, Koji
Chayama, Kazuaki
author_facet Yoshikawa, Yuki
Imamura, Michio
Yamauchi, Masami
Hayes, C. Nelson
Aikata, Hiroshi
Okamoto, Wataru
Miyata, Yoshihiro
Okada, Morihito
Hattori, Noboru
Sugiyama, Kazuhiko
Yoshioka, Yukio
Toratani, Shigeaki
Takechi, Masaaki
Ichinohe, Tatsuo
Ueda, Tsutomu
Takeno, Sachio
Kobayashi, Tsuyoshi
Ohdan, Hideki
Teishima, Jun
Hide, Michihiro
Nagata, Yasushi
Kudo, Yoshiki
Iida, Koji
Chayama, Kazuaki
author_sort Yoshikawa, Yuki
collection PubMed
description BACKGROUND: While immune checkpoint inhibitors (ICIs) occasionally cause immune-related adverse events (irAEs) in various organs, the prevalence of irAEs and potential risk factors have not been clarified. We identified irAE predictive factors and examined the relationship between the effect of ICIs and irAEs for patients with malignancies. METHODS: A total of 533 cases treated with ICIs, including programmed death 1 (PD-1), PD-ligand 1 (PD-L1), and cytotoxic T-lymphocyte antigen 4 (CTLA-4), for various malignancies were included retrospectively. We recorded irAEs from medical records and graded them using the Common Terminology Criteria for Adverse Events version 5. Prevalence and predictive factors associated with immune-related liver injury and the relationship between irAE and treatment response were analyzed. RESULTS: During a median of 10 (1–103) cycles with a median follow-up after several ICI initiations of 384 (21–1715) days, irAEs with all grades and with grade ≥ 3 developed in 144 (27.0%) and 57 (10.7%) cases. Cumulative irAE development rates were 21.9, 33.5, and 43.0% in all grades and 8.8, 14.9, and 20.7% in grade ≥ 3 at 5, 10, and 20 cycles, respectively. Patients who received anti-CTLA4 therapy were more likely to develop irAEs compared to those who received anti-PD-1 or anti-PD-L1 monotherapy. Liver injury was the most common irAE. Multivariate analysis identified the combination of PD-1 and anti-CTL-4 antibodies (hazard ratio [HR], 17.04; P < 0.0001) and baseline eosinophil count ≥130/μL (HR, 3.01 for < 130; P = 0.012) as independent risk factors for the incidence of immune-related liver injury with grade ≥ 2. Patients who developed irAEs had a higher disease control rate (P < 0.0001) and an increased overall survival rate compared to those without irAEs (P < 0.0001). CONCLUSION: Combination therapy with anti-PD-1 and anti-CTL-4 antibodies resulted in higher a frequency of irAEs. Baseline absolute eosinophil count was found to be a predictive factor for immune-related liver injury. Occurrence of irAEs may be associated with higher efficacy of ICI treatment and longer survival among patients who receive ICI therapy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-10327-7.
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spelling pubmed-97069842022-11-30 Prevalence of immune-related adverse events and anti-tumor efficacy following immune checkpoint inhibitor therapy in Japanese patients with various solid tumors Yoshikawa, Yuki Imamura, Michio Yamauchi, Masami Hayes, C. Nelson Aikata, Hiroshi Okamoto, Wataru Miyata, Yoshihiro Okada, Morihito Hattori, Noboru Sugiyama, Kazuhiko Yoshioka, Yukio Toratani, Shigeaki Takechi, Masaaki Ichinohe, Tatsuo Ueda, Tsutomu Takeno, Sachio Kobayashi, Tsuyoshi Ohdan, Hideki Teishima, Jun Hide, Michihiro Nagata, Yasushi Kudo, Yoshiki Iida, Koji Chayama, Kazuaki BMC Cancer Research BACKGROUND: While immune checkpoint inhibitors (ICIs) occasionally cause immune-related adverse events (irAEs) in various organs, the prevalence of irAEs and potential risk factors have not been clarified. We identified irAE predictive factors and examined the relationship between the effect of ICIs and irAEs for patients with malignancies. METHODS: A total of 533 cases treated with ICIs, including programmed death 1 (PD-1), PD-ligand 1 (PD-L1), and cytotoxic T-lymphocyte antigen 4 (CTLA-4), for various malignancies were included retrospectively. We recorded irAEs from medical records and graded them using the Common Terminology Criteria for Adverse Events version 5. Prevalence and predictive factors associated with immune-related liver injury and the relationship between irAE and treatment response were analyzed. RESULTS: During a median of 10 (1–103) cycles with a median follow-up after several ICI initiations of 384 (21–1715) days, irAEs with all grades and with grade ≥ 3 developed in 144 (27.0%) and 57 (10.7%) cases. Cumulative irAE development rates were 21.9, 33.5, and 43.0% in all grades and 8.8, 14.9, and 20.7% in grade ≥ 3 at 5, 10, and 20 cycles, respectively. Patients who received anti-CTLA4 therapy were more likely to develop irAEs compared to those who received anti-PD-1 or anti-PD-L1 monotherapy. Liver injury was the most common irAE. Multivariate analysis identified the combination of PD-1 and anti-CTL-4 antibodies (hazard ratio [HR], 17.04; P < 0.0001) and baseline eosinophil count ≥130/μL (HR, 3.01 for < 130; P = 0.012) as independent risk factors for the incidence of immune-related liver injury with grade ≥ 2. Patients who developed irAEs had a higher disease control rate (P < 0.0001) and an increased overall survival rate compared to those without irAEs (P < 0.0001). CONCLUSION: Combination therapy with anti-PD-1 and anti-CTL-4 antibodies resulted in higher a frequency of irAEs. Baseline absolute eosinophil count was found to be a predictive factor for immune-related liver injury. Occurrence of irAEs may be associated with higher efficacy of ICI treatment and longer survival among patients who receive ICI therapy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-10327-7. BioMed Central 2022-11-29 /pmc/articles/PMC9706984/ /pubmed/36447159 http://dx.doi.org/10.1186/s12885-022-10327-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Yoshikawa, Yuki
Imamura, Michio
Yamauchi, Masami
Hayes, C. Nelson
Aikata, Hiroshi
Okamoto, Wataru
Miyata, Yoshihiro
Okada, Morihito
Hattori, Noboru
Sugiyama, Kazuhiko
Yoshioka, Yukio
Toratani, Shigeaki
Takechi, Masaaki
Ichinohe, Tatsuo
Ueda, Tsutomu
Takeno, Sachio
Kobayashi, Tsuyoshi
Ohdan, Hideki
Teishima, Jun
Hide, Michihiro
Nagata, Yasushi
Kudo, Yoshiki
Iida, Koji
Chayama, Kazuaki
Prevalence of immune-related adverse events and anti-tumor efficacy following immune checkpoint inhibitor therapy in Japanese patients with various solid tumors
title Prevalence of immune-related adverse events and anti-tumor efficacy following immune checkpoint inhibitor therapy in Japanese patients with various solid tumors
title_full Prevalence of immune-related adverse events and anti-tumor efficacy following immune checkpoint inhibitor therapy in Japanese patients with various solid tumors
title_fullStr Prevalence of immune-related adverse events and anti-tumor efficacy following immune checkpoint inhibitor therapy in Japanese patients with various solid tumors
title_full_unstemmed Prevalence of immune-related adverse events and anti-tumor efficacy following immune checkpoint inhibitor therapy in Japanese patients with various solid tumors
title_short Prevalence of immune-related adverse events and anti-tumor efficacy following immune checkpoint inhibitor therapy in Japanese patients with various solid tumors
title_sort prevalence of immune-related adverse events and anti-tumor efficacy following immune checkpoint inhibitor therapy in japanese patients with various solid tumors
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9706984/
https://www.ncbi.nlm.nih.gov/pubmed/36447159
http://dx.doi.org/10.1186/s12885-022-10327-7
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