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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

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机构: [1]Cent South Univ, Hunan Canc Hosp, Affiliated Canc Hosp, Dept Thorac Oncol 2,Xiangya Sch Med, Changsha 410013, Peoples R China [2]Univ Elect Sci & Technol China, Sichuan Canc Ctr, Sch Med, Dept Med Oncol,Sichuan Canc Hosp & Inst, Chengdu 610000, Peoples R China [3]Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Shanghai 200030, Peoples R China [4]Chinese Acad Med Sci & Peking Union Med Coll, Canc Hosp, Natl Clin Res Ctr Canc, Dept Med Oncol,Natl Canc Ctr, Beijing 100005, Peoples R China [5]Chinese Univ Hong Kong, Dept Clin Oncol, State Key Lab Translat Oncol, Hong Kong 999077, Peoples R China [6]Kindai Univ Hosp, Dept Med, Osaka 5898511, Japan [7]Quiron Dexeus Univ Inst, Dr Rosell Oncol Inst, Barcelona 08028, Spain [8]Jilin Prov Canc Hosp, Changchun, Peoples R China [9]Third Mil Med Univ, Affiliated Hosp 1, Dept Pathol, Chongqing 400037, Peoples R China [10]San Camillo Forlanini Hosp, Pneumol Oncol, I-00152 Rome, Italy [11]Natl Canc Ctr Hosp East, Dept Thorac Oncol, Kashiwa 2778577, Japan [12]Chungbuk Natl Univ, Chungbuk Natl Univ Hosp, Coll Med, Cheongju 28644, South Korea [13]Clin Univ Navarra, Madrid 28027, Spain [14]Mar Sklodowska Curie Natl Res Inst Oncol, PL-02034 Warsaw, Poland [15]SFJ Pharmaceut Inc, Pleasanton, CA 94588 USA [16]Pfizer, Beijing 100010, Peoples R China [17]Pfizer, San Diego, CA 92121 USA
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关键词: ARCHER 1050 biomarker dacomitinib non-small-cell lung cancer skin disorders

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Aim: We investigated association between skin adverse events (AEs) and efficacy with dacomitinib in patients with EGFR-positive non-small-cell lung cancer (NSCLC). Methods: Post hoc 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. Results: 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. Conclusion: 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. Clinical Trial Registration: NCT01774721 (ClinicalTrials.gov)

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大类 | 4 区 医学
小类 | 4 区 肿瘤学
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Q2 ONCOLOGY

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第一作者机构: [1]Cent South Univ, Hunan Canc Hosp, Affiliated Canc Hosp, Dept Thorac Oncol 2,Xiangya Sch Med, Changsha 410013, Peoples R China
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