Efficacy in patients with <i>EGFR</i> -positive non-small-cell lung cancer treated with dacomitinib who had skin adverse events: <i>post hoc</i> analyses from ARCHER 1050

<b>Aim:</b> We investigated association between skin adverse events (AEs) and efficacy with dacomitinib in patients with <i>EGFR</i>-positive non-small-cell lung cancer (NSCLC).<b>Methods:</b> <i>Post hoc</i> analyses from ARCHER 1050 evaluated efficacy in patients who did and did not experience grade ≥2 skin AEs with dacomitinib. Landmark analyses were performed at 3 and 6 months.<b>Results:</b> In patients who had skin AEs (72.2%) vs. those who did not (27.7%), median progression-free survival was 16.0 vs. 9.2 months, median overall survival (OS) was 37.7 vs. 21.6 months, and objective response rate was 80.2 vs. 61.5%; OS was improved at 3 and 6 months landmark analyses.<b>Conclusion:</b> Presence of grade ≥2 skin AEs was associated with numerically improved efficacy and represents a valuable biomarker of treatment outcome with dacomitinib in patients with advanced NSCLC.<b>Clinical Trial Registration:</b> NCT01774721 (ClinicalTrials.gov).

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Publication Details

Journal
Future Oncology
Published
2024-10-03
DOI
https://doi.org/10.1080/14796694.2024.2404762
Citations
3
Primary Topic
Lung Cancer Treatments and Mutations
Type
article
Field-Weighted Citation Impact
1.26

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article

Efficacy in patients with EGFR -positive non-small-cell lung cancer treated with dacomitinib who had skin adverse events: post hoc analyses from ARCHER 1050

Weiwei Tan, Adam Płużański, Ki Hyeong Lee, R. Linke et al.
3 citations
Future Oncology
Lung Cancer Treatments and Mutations
1.26
article

Efficacy in patients with EGFR -positive non-small-cell lung cancer treated with dacomitinib who had skin adverse events: post hoc analyses from ARCHER 1050

Weiwei Tan, Adam Płużański, Ki Hyeong Lee, R. Linke, Yiyun Tang, Seiji Niho, Rafael Rosell, Ying Cheng, Xingxiang Pu, Tony Mok, Junling Li, Xiangdong Zhou, Lin Wu, Juan Li, Kazuhiko Nakagawa, Jinyao Zhang, Maria Rita Miglorino, J. Corral, Bo Zhang, Fang Pan
article en
3 citations

Abstract

<b>Aim:</b> We investigated association between skin adverse events (AEs) and efficacy with dacomitinib in patients with <i>EGFR</i>-positive non-small-cell lung cancer (NSCLC).<b>Methods:</b> <i>Post hoc</i> analyses from ARCHER 1050 evaluated efficacy in patients who did and did not experience grade ≥2 skin AEs with dacomitinib. Landmark analyses were performed at 3 and 6 months.<b>Results:</b> In patients who had skin AEs (72.2%) vs. those who did not (27.7%), median progression-free survival was 16.0 vs. 9.2 months, median overall survival (OS) was 37.7 vs. 21.6 months, and objective response rate was 80.2 vs. 61.5%; OS was improved at 3 and 6 months landmark analyses.<b>Conclusion:</b> Presence of grade ≥2 skin AEs was associated with numerically improved efficacy and represents a valuable biomarker of treatment outcome with dacomitinib in patients with advanced NSCLC.<b>Clinical Trial Registration:</b> NCT01774721 (ClinicalTrials.gov).

Future OncologyVol. 20(37)
Central South University (CN), Army Medical University (CN), Chinese University of Hong Kong (HK), Pfizer (United States) (US), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Shanghai Chest Hospital (CN), Kindai University Hospital (JP), Instituto Oncológico Dr. Rosell (ES), Hunan Cancer Hospital (CN), Sichuan Cancer Hospital (CN), Clinica Universidad de Navarra (ES), National Cancer Center Hospital East (JP), Pfizer (China) (CN), The Maria Sklodowska-Curie National Research Institute of Oncology (PL), Carlo Forlanini Hospital (IT), Chungbuk National University Hospital (KR)
Bristol-Myers Squibb, Eli Lilly and Company, Pfizer, AstraZeneca, Sanofi, Taiho Pharmaceutical, Kissei, BeiGene, Sysmex Corporation, Kyorin Pharmaceutical, Puma Biotechnology, Lunit, Eisai, Ono Pharmaceutical, SymBio Pharmaceuticals Limited, Novartis Pharma, Pfizer Japan, Chugai Pharmaceutical, MSD K.K., Eli Lilly Japan, Sanofi K.K., Daiichi Sankyo Europe
Good health and well-being
Openalex Percentile: Top 18%
Lung Cancer Treatments and Mutations
1.26
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