| Literature DB >> 22000810 |
Edith P Mitchell1, Bilal Piperdi, Mario E Lacouture, Heather Shearer, Nicholas Iannotti, Madhavan V Pillai, Feng Xu, Mohamed Yassine.
Abstract
BACKGROUND: Panitumumab, a fully human monoclonal antibody targeting the epidermal growth factor receptor (EGFR), is used as monotherapy for chemorefractory metastatic colorectal cancer (mCRC) in patients with wild-type (WT) KRAS tumors. Although skin toxicities are the most common adverse events associated with EGFR inhibitors, the differences in efficacy and safety between pre-emptive and reactive skin treatment according to KRAS tumor status has not been reported. PATIENTS AND METHODS: Eligible patients had mCRC with disease progression or unacceptable toxicity with first-line treatment containing fluoropyrimidine and oxaliplatin-based chemotherapy ± bevacizumab. Patients were randomized 1:1 to pre-emptive or reactive skin treatment (after skin toxicity developed). Patients received either panitumumab 6 mg/kg + FOLFIRI every 2 weeks or panitumumab 9 mg/kg + irinotecan every 3 weeks. Key study endpoints included overall response rate (ORR), overall survival, progression-free survival (PFS), and safety according to KRAS tumor status.Entities:
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Year: 2011 PMID: 22000810 DOI: 10.1016/j.clcc.2011.06.004
Source DB: PubMed Journal: Clin Colorectal Cancer ISSN: 1533-0028 Impact factor: 4.481