| Literature DB >> 27287210 |
M E Lacouture1, D M Keefe2, S Sonis3, A Jatoi4, D Gernhardt5, T Wang5, J P Doherty6, N Giri7, S Nadanaciva5, J O'Connell6, E Sbar8, B Piperdi9, E B Garon10.
Abstract
BACKGROUND: ARCHER 1042, a randomized phase II trial, explored the impact of prophylactic treatment on select dermatologic adverse events of interest (SDAEI), diarrhea, and mucositis associated with dacomitinib, an oral irreversible pan-human epidermal growth factor receptor (HER) inhibitor, in development for advanced non-small-cell lung cancer (NSCLC). PATIENTS AND METHODS: Patients with advanced NSCLC treated with dacomitinib were enrolled in two cohorts. Cohort I patients were randomized 1:1 to receive oral doxycycline or placebo (4 weeks). Cohort II patients received oral VSL#3 probiotic plus topical alclometasone. Primary end points for Cohorts I and II were incidence of all grade and grade ≥2 SDAEI in the first 8 weeks of treatment and quality of life (QoL) assessed by the Skindex-16 survey. Additional primary end points for Cohort II were incidence of all grade and grade ≥2 diarrhea and mucositis in the first 8 weeks of treatment; QoL regarding diarrhea and mucositis incidence was assessed by the modified-Oral Mucositis Daily Questionnaire.Entities:
Keywords: dacomitinib; dermatologic adverse events; epidermal growth factor receptor; gastrointestinal adverse events; non-small-cell lung cancer
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Year: 2016 PMID: 27287210 PMCID: PMC6279098 DOI: 10.1093/annonc/mdw227
Source DB: PubMed Journal: Ann Oncol ISSN: 0923-7534 Impact factor: 32.976