U.S. Food and Drug Administration approval summary: Erlotinib for the first-line treatment of metastatic non-small cell lung cancer with epidermal growth factor receptor exon 19 deletions or exon 21 (L858R) substitution mutations.

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Published in Oncologist on May 27, 2014

Authors

Sean Khozin1, Gideon M Blumenthal2, Xiaoping Jiang2, Kun He2, Karen Boyd2, Anthony Murgo2, Robert Justice2, Patricia Keegan2, Richard Pazdur2

Author Affiliations

1: Office of Hematology and Oncology Products, Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, Maryland, USA sean.khozin@fda.hhs.gov.
2: Office of Hematology and Oncology Products, Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, Maryland, USA.

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