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KRAS codon 61, 146 and BRAF mutations predict resistance to cetuximab plus irinotecan in KRAS codon 12 and 13 wild-type metastatic colorectal cancer.
| Content Provider | Europe PMC |
|---|---|
| Author | Loupakis, F Ruzzo, A Cremolini, C Vincenzi, B Salvatore, L Santini, D Masi, G Stasi, I Canestrari, E Rulli, E Floriani, I Bencardino, K Galluccio, N Catalano, V Tonini, G Magnani, M Fontanini, G Basolo, F Falcone, A Graziano, F |
| Copyright Year | 2009 |
| Abstract | Background:KRAS codons 12 and 13 mutations predict resistance to anti-EGFR monoclonal antibodies (moAbs) in metastatic colorectal cancer. Also, BRAF V600E mutation has been associated with resistance. Additional KRAS mutations are described in CRC.Methods:We investigated the role of KRAS codons 61 and 146 and BRAF V600E mutations in predicting resistance to cetuximab plus irinotecan in a cohort of KRAS codons 12 and 13 wild-type patients.Results:Among 87 KRAS codons 12 and 13 wild-type patients, KRAS codons 61 and 146 were mutated in 7 and 1 case, respectively. None of mutated patients responded vs 22 of 68 wild type (P=0.096). Eleven patients were not evaluable. KRAS mutations were associated with shorter progression-free survival (PFS, HR: 0.46, P=0.028). None of 13 BRAF-mutated patients responded vs 24 of 74 BRAF wild type (P=0.016). BRAF mutation was associated with a trend towards shorter PFS (HR: 0.59, P=0.073). In the subgroup of BRAF wild-type patients, KRAS codons 61/146 mutations determined a lower response rate (0 vs 37%, P=0.047) and worse PFS (HR: 0.45, P=0.023). Patients bearing KRAS or BRAF mutations had poorer response rate (0 vs 37%, P=0.0005) and PFS (HR: 0.51, P=0.006) compared with KRAS and BRAF wild-type patients.Conclusion:Assessing KRAS codons 61/146 and BRAF V600E mutations might help optimising the selection of the candidate patients to receive anti-EGFR moAbs. |
| ISSN | 00070920 |
| Journal | British Journal of Cancer |
| Volume Number | 101 |
| PubMed Central reference number | PMC2736831 |
| Issue Number | 4 |
| PubMed reference number | 19603018 |
| e-ISSN | 15321827 |
| DOI | 10.1038/sj.bjc.6605177 |
| Language | English |
| Publisher | Nature Publishing Group |
| Publisher Date | 2009-07-14 |
| Access Restriction | Open |
| Rights License | This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. Copyright © 2009 Cancer Research UK |
| Subject Keyword | colorectal cancer cetuximab KRAS BRAF |
| Content Type | Text |
| Resource Type | Article |
| Subject | Cancer Research Oncology |