Global named patient use program of afatinib in advanced non-small-cell lung carcinoma patients who progressed following prior therapies
Author(s) -
Federico Cappuzzo,
Ross A. Soo,
Maximilian J. Hochmair,
Martin Schüler,
Kwok Chi Lam,
G. Stehle,
A. Cseh,
Robert M. Lorence,
Stephan Linden,
Nicole D Forman,
Wolfgang Hilbe,
Abdul Rahman Jazieh,
ChunMing Tsai
Publication year - 2018
Publication title -
future oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.857
H-Index - 72
eISSN - 1744-8301
pISSN - 1479-6694
DOI - 10.2217/fon-2017-0666
Subject(s) - afatinib , medicine , erlotinib , gefitinib , oncology , lung cancer , clinical trial , carcinoma , epidermal growth factor receptor , cancer
Aim: A global afatinib named patient use program in non-small-cell lung carcinoma (NSCLC) commenced in 2010. Materials & methods: Eligible NSCLC patients had progressed after clinical benefit on prior erlotinib/gefitinib and/or had activating EGFR/HER2 mutations, exhausted all other treatments, and were ineligible for afatinib trials. Results: Data, as of January 2016, were reported on 3966 heavily pretreated NSCLC patients (41 countries; six continents). Among 2595/3966 (65.4%) patients with tumor EGFR status, 2407 (92.8%) were EGFR mutation positive. Median time to treatment failure (2862/3966 [72.2%] patients with available data) was 4.4 months. Among 1141/2862 (39.9%) patients with response reported, objective response rate was 23.4% (267/1141). Safety findings were as expected. Conclusion: Time to treatment failure durations and objective response rates were encouraging.
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