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晚期非小细胞肺癌患者应用免疫治疗后出现甲状腺功能异常与疗效的相关性分析
Background and objective Thyroid function abnormality (TFA) is one of the common adverse reactions in patients with advanced non-small cell lung cancer (NSCLC) treated with immunotherapy, but the risk factors of TFA and its relationship with efficacy are not completely clear. The purpose of this stu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Editorial board of Chinese Journal of Lung Cancer
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10273147/ https://www.ncbi.nlm.nih.gov/pubmed/37316446 http://dx.doi.org/10.3779/j.issn.1009-3419.2023.106.09 |
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author | Yibo, WANG Xinjuan, WANG Lin, CHENG Guojun, ZHANG |
author_facet | Yibo, WANG Xinjuan, WANG Lin, CHENG Guojun, ZHANG |
author_sort | Yibo, WANG |
collection | PubMed |
description | Background and objective Thyroid function abnormality (TFA) is one of the common adverse reactions in patients with advanced non-small cell lung cancer (NSCLC) treated with immunotherapy, but the risk factors of TFA and its relationship with efficacy are not completely clear. The purpose of this study was to explore the risk factors of TFA and its relationship with efficacy in patients with advanced NSCLC after immunotherapy. Methods The general clinical data of 200 patients with advanced NSCLC in The First Affiliated Hospital of Zhengzhou University from July 1, 2019 to June 31, 2021 were collected and analyzed retrospectively. χ² test and multivariate Logistic regression were used to explore the risk factors of TFA. Kaplan-Meier curve was drawn and Log-rank test was used for comparison between groups. Univariate and multivariate Cox analysis was used to explore the efficacy factors. Results A total of 86 (43.0%) patients developed TFA. Logistic regression analysis showed that Eastern Cooperative Oncology Group Performance Status (ECOG PS), pleural effusion and lactic dehydrogenase (LDH) were factors influencing TFA (P<0.05). Compared with normal thyroid function group, the median progression-free survival (PFS) of patients in the TFA group was significantly longer (19.0 months vs 6.3 months, P<0.001), and the objective response rate (ORR) (65.1% vs 28.9%, P=0.020) and disease control rate (DCR) (100.0% vs 92.1%, P=0.020) of the TFA group were better than those of the normal thyroid function group. Cox regression analysis showed that ECOG PS, LDH, cytokeratin 19 fragment (CYFRA21-1) and TFA were factors influencing prognosis (P<0.05). Conclusion ECOG PS, pleural effusion and LDH may be risk factors affecting the occurrence of TFA and TFA may be a predictor of the efficacy of immunotherapy. Patients with advanced NSCLC who have TFA after immunotherapy may obtain better efficacy. |
format | Online Article Text |
id | pubmed-10273147 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Editorial board of Chinese Journal of Lung Cancer |
record_format | MEDLINE/PubMed |
spelling | pubmed-102731472023-06-17 晚期非小细胞肺癌患者应用免疫治疗后出现甲状腺功能异常与疗效的相关性分析 Yibo, WANG Xinjuan, WANG Lin, CHENG Guojun, ZHANG Zhongguo Fei Ai Za Zhi Clinical Research Background and objective Thyroid function abnormality (TFA) is one of the common adverse reactions in patients with advanced non-small cell lung cancer (NSCLC) treated with immunotherapy, but the risk factors of TFA and its relationship with efficacy are not completely clear. The purpose of this study was to explore the risk factors of TFA and its relationship with efficacy in patients with advanced NSCLC after immunotherapy. Methods The general clinical data of 200 patients with advanced NSCLC in The First Affiliated Hospital of Zhengzhou University from July 1, 2019 to June 31, 2021 were collected and analyzed retrospectively. χ² test and multivariate Logistic regression were used to explore the risk factors of TFA. Kaplan-Meier curve was drawn and Log-rank test was used for comparison between groups. Univariate and multivariate Cox analysis was used to explore the efficacy factors. Results A total of 86 (43.0%) patients developed TFA. Logistic regression analysis showed that Eastern Cooperative Oncology Group Performance Status (ECOG PS), pleural effusion and lactic dehydrogenase (LDH) were factors influencing TFA (P<0.05). Compared with normal thyroid function group, the median progression-free survival (PFS) of patients in the TFA group was significantly longer (19.0 months vs 6.3 months, P<0.001), and the objective response rate (ORR) (65.1% vs 28.9%, P=0.020) and disease control rate (DCR) (100.0% vs 92.1%, P=0.020) of the TFA group were better than those of the normal thyroid function group. Cox regression analysis showed that ECOG PS, LDH, cytokeratin 19 fragment (CYFRA21-1) and TFA were factors influencing prognosis (P<0.05). Conclusion ECOG PS, pleural effusion and LDH may be risk factors affecting the occurrence of TFA and TFA may be a predictor of the efficacy of immunotherapy. Patients with advanced NSCLC who have TFA after immunotherapy may obtain better efficacy. Editorial board of Chinese Journal of Lung Cancer 2023-05-20 /pmc/articles/PMC10273147/ /pubmed/37316446 http://dx.doi.org/10.3779/j.issn.1009-3419.2023.106.09 Text en Copyright © 2023《中国肺癌杂志》编辑部 https://creativecommons.org/licenses/by/3.0/This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/. |
spellingShingle | Clinical Research Yibo, WANG Xinjuan, WANG Lin, CHENG Guojun, ZHANG 晚期非小细胞肺癌患者应用免疫治疗后出现甲状腺功能异常与疗效的相关性分析 |
title | 晚期非小细胞肺癌患者应用免疫治疗后出现甲状腺功能异常与疗效的相关性分析 |
title_full | 晚期非小细胞肺癌患者应用免疫治疗后出现甲状腺功能异常与疗效的相关性分析 |
title_fullStr | 晚期非小细胞肺癌患者应用免疫治疗后出现甲状腺功能异常与疗效的相关性分析 |
title_full_unstemmed | 晚期非小细胞肺癌患者应用免疫治疗后出现甲状腺功能异常与疗效的相关性分析 |
title_short | 晚期非小细胞肺癌患者应用免疫治疗后出现甲状腺功能异常与疗效的相关性分析 |
title_sort | 晚期非小细胞肺癌患者应用免疫治疗后出现甲状腺功能异常与疗效的相关性分析 |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10273147/ https://www.ncbi.nlm.nih.gov/pubmed/37316446 http://dx.doi.org/10.3779/j.issn.1009-3419.2023.106.09 |
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