4.7 Review

KRAS mutations: Analytical considerations

Journal

CLINICA CHIMICA ACTA
Volume 431, Issue -, Pages 211-220

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.cca.2014.01.049

Keywords

Colorectal cancer; KRAS gene; Mutation; Method and mutation analysis

Funding

  1. Kaohsiung Medical University Hospital [KMUH102-M207]
  2. Ministry of Health and Welfare [MOHW103-TD-B-111-05]

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Colorectal cancer (CRC) is the third most common cancer and the second most common cause of cancer death globally. Significant improvements in survival have been made in patients with metastasis by new therapies. For example, Cetuximab and Panitumumab are monoclonal antibodies that inhibit the epidermal growth receptor (EGFR). KRAS mutations in codon 12 and 13 are the recognized biomarkers that are analyzed in clinics before the administration of anti-EGFR therapy. Genetic analyses have revealed that mutations in KRAS predict a lack of response to Panitumumab and Cetuximab in patients with metastatic CRC (mCRC). Notably, it is estimated that 35-45% of CRC patients harbor KRAS mutations. Therefore, KRAS mutation testing should be performed in all individuals with the advanced CRC in order to identify the patients who will not respond to the monoclonal EGFR antibody inhibitors. New techniques for KRAS testing have arisen rapidly, and each technique has advantages and disadvantages. Herein, we review the latest published literature specific to KRAS mutation testing techniques. Since reliability and feasibility are important issues in clinical analyses. Therefore, this review also summarizes the effectiveness and limitations of numerous KRAS mutation testing techniques. (C) 2014 Elsevier B.V. All rights reserved.

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