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Efficacy of dacomitinib in patients with non-small cell lung cancer carrying complex EGFR mutations: a real-world study

BACKGROUND: Dacomitinib is a first-line treatment for patients with non-small cell lung cancer (NSCLC) harboring common epidermal growth factor receptor (EGFR) mutations; however, clinical evidence of its activity on NSCLC with complex EGFR mutations is limited. METHODS: Patients harboring complex (...

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Autores principales: Li, Hong-Shuai, Li, Jun-Ling, Yan, Xiang, Xu, Hai-Yan, Zhou, Li-Qiang, Hu, Xing-Sheng, Wang, Yu-Ying, Lei, Si-Yu, Wang, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9186228/
https://www.ncbi.nlm.nih.gov/pubmed/35693621
http://dx.doi.org/10.21037/jtd-21-1841
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author Li, Hong-Shuai
Li, Jun-Ling
Yan, Xiang
Xu, Hai-Yan
Zhou, Li-Qiang
Hu, Xing-Sheng
Wang, Yu-Ying
Lei, Si-Yu
Wang, Yan
author_facet Li, Hong-Shuai
Li, Jun-Ling
Yan, Xiang
Xu, Hai-Yan
Zhou, Li-Qiang
Hu, Xing-Sheng
Wang, Yu-Ying
Lei, Si-Yu
Wang, Yan
author_sort Li, Hong-Shuai
collection PubMed
description BACKGROUND: Dacomitinib is a first-line treatment for patients with non-small cell lung cancer (NSCLC) harboring common epidermal growth factor receptor (EGFR) mutations; however, clinical evidence of its activity on NSCLC with complex EGFR mutations is limited. METHODS: Patients harboring complex (common mutations co-existing with uncommon mutations), or common (comparison cohort) EGFR mutations, who were treated with dacomitinib, were retrospectively evaluated in the Chinese National Cancer Center and the China PLA hospital between August 2019 and August 2021. RESULTS: In total, 72 patients with NSCLC harboring complex (C+U group, n=18) or common (C group, n=54) EGFR mutations and being treated with dacomitinib were enrolled. In the C+U group, 16 cases (88.9%) harbored L858R mutations co-existing with uncommon mutations located from exon 18 to exon 25 of EGFR (mostly E709X), and two cases harbored exon 19 deletion co-existing with G724S or K754E. Among the 15 evaluable patients, the objective response rate (ORR) was 40% (6/15), and the disease control rate (DCR) was 73.3% (11/15). The median progression-free survival (PFS) was 7.5 months [95% confidence interval (CI), 4.4–10.6 months]. Except for the application line of dacomitinib (P=0.039), no significant statistical differences were found in other characteristics and adverse events between the two groups. The Kaplan-Meier method revealed no significant differences in PFS (P=0.889) and overall survival (OS) (P=0.703). However, the stratified analysis found worse PFS in the C+U group than that observed in the C group when receiving 1(st) and ≥3(rd) line dacomitinib treatment, while its OS was worse than that of group C when receiving ≥3(rd) line treatment. Furthermore, in a multivariate analysis, complex mutation status was an independent prognostic factor for OS (P=0.038) in the entire cohort. CONCLUSIONS: This study indicated a worse response and prognosis of patients with NSCLC harboring complex EGFR mutations than those harboring common EGFR mutations when treated with dacomitinib. Further studies and data are needed to confirm this conclusion.
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spelling pubmed-91862282022-06-11 Efficacy of dacomitinib in patients with non-small cell lung cancer carrying complex EGFR mutations: a real-world study Li, Hong-Shuai Li, Jun-Ling Yan, Xiang Xu, Hai-Yan Zhou, Li-Qiang Hu, Xing-Sheng Wang, Yu-Ying Lei, Si-Yu Wang, Yan J Thorac Dis Original Article BACKGROUND: Dacomitinib is a first-line treatment for patients with non-small cell lung cancer (NSCLC) harboring common epidermal growth factor receptor (EGFR) mutations; however, clinical evidence of its activity on NSCLC with complex EGFR mutations is limited. METHODS: Patients harboring complex (common mutations co-existing with uncommon mutations), or common (comparison cohort) EGFR mutations, who were treated with dacomitinib, were retrospectively evaluated in the Chinese National Cancer Center and the China PLA hospital between August 2019 and August 2021. RESULTS: In total, 72 patients with NSCLC harboring complex (C+U group, n=18) or common (C group, n=54) EGFR mutations and being treated with dacomitinib were enrolled. In the C+U group, 16 cases (88.9%) harbored L858R mutations co-existing with uncommon mutations located from exon 18 to exon 25 of EGFR (mostly E709X), and two cases harbored exon 19 deletion co-existing with G724S or K754E. Among the 15 evaluable patients, the objective response rate (ORR) was 40% (6/15), and the disease control rate (DCR) was 73.3% (11/15). The median progression-free survival (PFS) was 7.5 months [95% confidence interval (CI), 4.4–10.6 months]. Except for the application line of dacomitinib (P=0.039), no significant statistical differences were found in other characteristics and adverse events between the two groups. The Kaplan-Meier method revealed no significant differences in PFS (P=0.889) and overall survival (OS) (P=0.703). However, the stratified analysis found worse PFS in the C+U group than that observed in the C group when receiving 1(st) and ≥3(rd) line dacomitinib treatment, while its OS was worse than that of group C when receiving ≥3(rd) line treatment. Furthermore, in a multivariate analysis, complex mutation status was an independent prognostic factor for OS (P=0.038) in the entire cohort. CONCLUSIONS: This study indicated a worse response and prognosis of patients with NSCLC harboring complex EGFR mutations than those harboring common EGFR mutations when treated with dacomitinib. Further studies and data are needed to confirm this conclusion. AME Publishing Company 2022-05 /pmc/articles/PMC9186228/ /pubmed/35693621 http://dx.doi.org/10.21037/jtd-21-1841 Text en 2022 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
Li, Hong-Shuai
Li, Jun-Ling
Yan, Xiang
Xu, Hai-Yan
Zhou, Li-Qiang
Hu, Xing-Sheng
Wang, Yu-Ying
Lei, Si-Yu
Wang, Yan
Efficacy of dacomitinib in patients with non-small cell lung cancer carrying complex EGFR mutations: a real-world study
title Efficacy of dacomitinib in patients with non-small cell lung cancer carrying complex EGFR mutations: a real-world study
title_full Efficacy of dacomitinib in patients with non-small cell lung cancer carrying complex EGFR mutations: a real-world study
title_fullStr Efficacy of dacomitinib in patients with non-small cell lung cancer carrying complex EGFR mutations: a real-world study
title_full_unstemmed Efficacy of dacomitinib in patients with non-small cell lung cancer carrying complex EGFR mutations: a real-world study
title_short Efficacy of dacomitinib in patients with non-small cell lung cancer carrying complex EGFR mutations: a real-world study
title_sort efficacy of dacomitinib in patients with non-small cell lung cancer carrying complex egfr mutations: a real-world study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9186228/
https://www.ncbi.nlm.nih.gov/pubmed/35693621
http://dx.doi.org/10.21037/jtd-21-1841
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