Cargando…
Comparison of first-generation EGFR-TKIs (gefitinib, erlotinib, and icotinib) as adjuvant therapy in resected NSCLC patients with sensitive EGFR mutations
BACKGROUND: Several randomized controlled trials have suggested that adjuvant epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) were associated with prolonged disease-free survival (DFS) in EGFR-mutated NSCLC patients after radical resection, comparing with chemotherapy or pl...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8674600/ https://www.ncbi.nlm.nih.gov/pubmed/35004243 http://dx.doi.org/10.21037/tlcr-21-649 |
_version_ | 1784615706668564480 |
---|---|
author | He, Qihua Liu, Jun Cai, Xiuyu He, Miao Li, Caichen Liang, Hengrui Cheng, Bo Xia, Xiaojun Guo, Minzhang Liang, Peng Zhong, Ran Li, Feng Yu, Ziwen Zhao, Yi Ou, Limin Xiong, Shan Li, Jianfu Zhang, Jianrong He, Jianxing Liang, Wenhua |
author_facet | He, Qihua Liu, Jun Cai, Xiuyu He, Miao Li, Caichen Liang, Hengrui Cheng, Bo Xia, Xiaojun Guo, Minzhang Liang, Peng Zhong, Ran Li, Feng Yu, Ziwen Zhao, Yi Ou, Limin Xiong, Shan Li, Jianfu Zhang, Jianrong He, Jianxing Liang, Wenhua |
author_sort | He, Qihua |
collection | PubMed |
description | BACKGROUND: Several randomized controlled trials have suggested that adjuvant epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) were associated with prolonged disease-free survival (DFS) in EGFR-mutated NSCLC patients after radical resection, comparing with chemotherapy or placebo. We aimed to compare the effectiveness of different first-generation EGFR-TKIs as adjuvant treatment in real-world setting. METHODS: Early-stage EGFR mutated NSCLC patients who underwent radical resection and treated with first-generation EGFR-TKIs (gefitinib, erlotinib, icotinib) as adjuvant therapy between Feb 2010 and Jan 2019 were retrieved from a prospectively-maintained database in our center. The primary endpoint was DFS in stage II/III (TNM 8th) patients with exploratory endpoint regarding DFS in stage I patients. Sensitivity analyses were based on propensity score matched (PSM) cohorts. Treatment failure patterns among different TKIs were also compared. RESULTS: Of 588 eligible patients, 198 patients (33.7%) received gefitinib, 106 patients (17.9%) received erlotinib, and 284 patients (48.2%) received icotinib. The median DFS of stage II/III patients in the gefitinib, erlotinib and icotinib group were 36.1 months (95% CI, 23.9–49.4), 42.8 months (95% CI, 29.6–97.8), and 32.5 months (95% CI, 23.9–49.4), respectively, with no significant difference (log-rank test P=0.22). There was also no significant difference in DFS among stage I patients receiving different TKIs (P=0.12). PSM adjustments and multivariate analyses adjusting for other confounders revealed similar results. In addition, there were no significant differences in treatment failure pattens in different EGFR-TKI arms, especially in terms of brain metastases (6.1% in gefitinb, 7.5% in erlotinib, 3.9% in icotinib) and bone metastases (8.6% in gefitinb, 9.4% in erlotinib, 7.0% in icotinib). CONCLUSIONS: This first and largest real-world study showed that gefitinib, erlotinib, and icotinib demonstrated comparable clinical effectiveness as adjuvant therapy for patients with early-stage EGFR mutated NSCLC. |
format | Online Article Text |
id | pubmed-8674600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-86746002022-01-06 Comparison of first-generation EGFR-TKIs (gefitinib, erlotinib, and icotinib) as adjuvant therapy in resected NSCLC patients with sensitive EGFR mutations He, Qihua Liu, Jun Cai, Xiuyu He, Miao Li, Caichen Liang, Hengrui Cheng, Bo Xia, Xiaojun Guo, Minzhang Liang, Peng Zhong, Ran Li, Feng Yu, Ziwen Zhao, Yi Ou, Limin Xiong, Shan Li, Jianfu Zhang, Jianrong He, Jianxing Liang, Wenhua Transl Lung Cancer Res Original Article BACKGROUND: Several randomized controlled trials have suggested that adjuvant epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) were associated with prolonged disease-free survival (DFS) in EGFR-mutated NSCLC patients after radical resection, comparing with chemotherapy or placebo. We aimed to compare the effectiveness of different first-generation EGFR-TKIs as adjuvant treatment in real-world setting. METHODS: Early-stage EGFR mutated NSCLC patients who underwent radical resection and treated with first-generation EGFR-TKIs (gefitinib, erlotinib, icotinib) as adjuvant therapy between Feb 2010 and Jan 2019 were retrieved from a prospectively-maintained database in our center. The primary endpoint was DFS in stage II/III (TNM 8th) patients with exploratory endpoint regarding DFS in stage I patients. Sensitivity analyses were based on propensity score matched (PSM) cohorts. Treatment failure patterns among different TKIs were also compared. RESULTS: Of 588 eligible patients, 198 patients (33.7%) received gefitinib, 106 patients (17.9%) received erlotinib, and 284 patients (48.2%) received icotinib. The median DFS of stage II/III patients in the gefitinib, erlotinib and icotinib group were 36.1 months (95% CI, 23.9–49.4), 42.8 months (95% CI, 29.6–97.8), and 32.5 months (95% CI, 23.9–49.4), respectively, with no significant difference (log-rank test P=0.22). There was also no significant difference in DFS among stage I patients receiving different TKIs (P=0.12). PSM adjustments and multivariate analyses adjusting for other confounders revealed similar results. In addition, there were no significant differences in treatment failure pattens in different EGFR-TKI arms, especially in terms of brain metastases (6.1% in gefitinb, 7.5% in erlotinib, 3.9% in icotinib) and bone metastases (8.6% in gefitinb, 9.4% in erlotinib, 7.0% in icotinib). CONCLUSIONS: This first and largest real-world study showed that gefitinib, erlotinib, and icotinib demonstrated comparable clinical effectiveness as adjuvant therapy for patients with early-stage EGFR mutated NSCLC. AME Publishing Company 2021-11 /pmc/articles/PMC8674600/ /pubmed/35004243 http://dx.doi.org/10.21037/tlcr-21-649 Text en 2021 Translational Lung Cancer Research. 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 He, Qihua Liu, Jun Cai, Xiuyu He, Miao Li, Caichen Liang, Hengrui Cheng, Bo Xia, Xiaojun Guo, Minzhang Liang, Peng Zhong, Ran Li, Feng Yu, Ziwen Zhao, Yi Ou, Limin Xiong, Shan Li, Jianfu Zhang, Jianrong He, Jianxing Liang, Wenhua Comparison of first-generation EGFR-TKIs (gefitinib, erlotinib, and icotinib) as adjuvant therapy in resected NSCLC patients with sensitive EGFR mutations |
title | Comparison of first-generation EGFR-TKIs (gefitinib, erlotinib, and icotinib) as adjuvant therapy in resected NSCLC patients with sensitive EGFR mutations |
title_full | Comparison of first-generation EGFR-TKIs (gefitinib, erlotinib, and icotinib) as adjuvant therapy in resected NSCLC patients with sensitive EGFR mutations |
title_fullStr | Comparison of first-generation EGFR-TKIs (gefitinib, erlotinib, and icotinib) as adjuvant therapy in resected NSCLC patients with sensitive EGFR mutations |
title_full_unstemmed | Comparison of first-generation EGFR-TKIs (gefitinib, erlotinib, and icotinib) as adjuvant therapy in resected NSCLC patients with sensitive EGFR mutations |
title_short | Comparison of first-generation EGFR-TKIs (gefitinib, erlotinib, and icotinib) as adjuvant therapy in resected NSCLC patients with sensitive EGFR mutations |
title_sort | comparison of first-generation egfr-tkis (gefitinib, erlotinib, and icotinib) as adjuvant therapy in resected nsclc patients with sensitive egfr mutations |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8674600/ https://www.ncbi.nlm.nih.gov/pubmed/35004243 http://dx.doi.org/10.21037/tlcr-21-649 |
work_keys_str_mv | AT heqihua comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations AT liujun comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations AT caixiuyu comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations AT hemiao comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations AT licaichen comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations AT lianghengrui comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations AT chengbo comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations AT xiaxiaojun comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations AT guominzhang comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations AT liangpeng comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations AT zhongran comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations AT lifeng comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations AT yuziwen comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations AT zhaoyi comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations AT oulimin comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations AT xiongshan comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations AT lijianfu comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations AT zhangjianrong comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations AT hejianxing comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations AT liangwenhua comparisonoffirstgenerationegfrtkisgefitiniberlotinibandicotinibasadjuvanttherapyinresectednsclcpatientswithsensitiveegfrmutations |