articleNew England Journal of MedicineSep 11, 2013BRONZE OA

Panitumumab–FOLFOX4 Treatment and RAS Mutations in Colorectal Cancer

Institut de Cancérologie de l'Ouest

PubMed
Indexed incrossrefpubmed

Abstract

Background

Patients with metastatic colorectal cancer that harbors KRAS mutations in exon 2 do not benefit from anti-epidermal growth factor receptor (EGFR) therapy. Other activating RAS mutations may also be negative predictive biomarkers for anti-EGFR therapy.

Methods

In this prospective-retrospective analysis, we assessed the efficacy and safety of panitumumab plus oxaliplatin, fluorouracil, and leucovorin (FOLFOX4) as compared with FOLFOX4 alone, according to RAS (KRAS or NRAS) or BRAF mutation status. A total of 639 patients who had metastatic colorectal cancer without KRAS mutations in exon 2 had results for at least one of the following: KRAS exon 3 or 4; NRAS exon 2, 3, or 4; or BRAF exon 15. The overall rate of ascertainment of RAS status was 90%.

Citation impact

2,241
total citations
FWCI
125.53
Percentile
100%
References
31
Citations per year

Authors

22

Topics & keywords

Keywords
  • KRAS
  • Panitumumab
  • Neuroblastoma RAS viral oncogene homolog
  • Medicine
  • Colorectal cancer
  • Hazard ratio
  • Internal medicine
  • Oncology
UN Sustainable Development Goals
  • Good health and well-being
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