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The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.

KRAS Mutations As an Independent Prognostic Factor in Patients With Advanced Colorectal Cancer Treated With Cetuximab

Lièvre, Astrid, Bachet, Jean-Baptiste, Boige, Valérie, Cayre, Anne, Le Corre, Delphine, Buc, Emmanuel, Ychou, Marc, Bouché, Olivier, Landi, Bruno, Louvet, Christophe, André, Thierry, Bibeau, Fréderic, Diebold, Marie-Danièle, Rougier, Philippe, Ducreux, Michel, Tomasic, Gorana, Emile, Jean-François, Penault-Llorca, Frédérique, Laurent-Puig, Pierre·2008·Journal of Clinical Oncology

Abstract

Purpose: Cetuximab is efficient in advanced colorectal cancer (CRC). We previously showed that KRAS mutations were associated with resistance to cetuximab in 30 CRC patients. The aim of this study was to validate, in an independent larger series of 89 patients, the prognostic value of KRAS mutations on response to cetuximab and survival. Patients and Methods: Eighty-nine metastatic CRC patients treated with cetuximab after treatment failure with irinotecan-based chemotherapy were analyzed for KRAS mutation by allelic discrimination on tumor DNA. The association between KRAS mutations and tumor response, skin toxicity, progression-free survival (PFS) and overall survival (OS) was analyzed. Results: A KRAS mutation was present in 27% of the patients and was associated with resistance to cetuximab (0% v 40% of responders among the 24 mutated and 65 nonmutated patients, respectively; P < .001) and a poorer survival (median PFS: 10.1 v 31.4 weeks in patients without mutation; P = .0001; median OS: 10.1 v 14.3 months in patients without mutation; P = .026). When we pooled these 89 patients with patients from our previous study, the multivariate analysis showed that KRAS status was an independent prognostic factor associated with OS and PFS, whereas skin toxicity was only associated with OS. In a combined analysis, median OS times of patients with two, one, or no favorable prognostic factors (severe skin toxicity and no KRAS mutation) was of 15.6, 10.7, and 5.6 months, respectively. Conclusion: These results confirm the high prognostic value of KRAS mutations on response to cetuximab and survival in metastatic CRC patients treated with cetuximab.

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  1. 10.1200/JCO.2000.18.16.2938 · DOI · Paper page
  2. 10.1016/S0140-6736(00)02034-1 · DOI · Paper page
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  12. Penault-Llorca F, Cayre A, Arnould L, et al: Is there an immunohistochemical technique definitively valid in epidermal growth factor receptor assessment? Oncol Rep 16:1173,2006-1179, · DOI
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  17. Tejpar S, Peeters M, Humblet Y, et al: Phase I/II study of cetuximab dose-escalation in patients with metastatic colorectal cancer (mCRC) with no or slight skin reactions on cetuximab standard dose treatment (EVEREST): Pharmacokinetic (PK), pharmacodynamic (PD) and efficacy data. J Clin Oncol 25:172s,2007, (suppl, abstr 4037) · DOI

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Metadata

Authors
Lièvre, A., Bachet, J.-B., Boige, V., Cayre, A., Le Corre, D., Buc, E., Ychou, M., Bouché, O., Landi, B., Louvet, C., André, T., Bibeau, F., Diebold, M.-D., Rougier, P., Ducreux, M., Tomasic, G., Emile, J.-F., Penault-Llorca, F., & Laurent-Puig, P.
Venue
Journal of Clinical Oncology
Published
2008-01-20
Volume
26
Issue
3
Pages
374-379
ISSN
  • 0732-183X (ISSN-L)
  • 1527-7755
OpenAlex
W2120490763
Cited by
1,444
References
6
FWCI
95.78
Type
journal article
Language
en
Open access
closed

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The paper
Lièvre, A., Bachet, J.-B., Boige, V., Cayre, A., Le Corre, D., Buc, E., Ychou, M., Bouché, O., Landi, B., Louvet, C., André, T., Bibeau, F., Diebold, M.-D., Rougier, P., Ducreux, M., Tomasic, G., Emile, J.-F., Penault-Llorca, F., & Laurent-Puig, P. (2008). KRAS Mutations As an Independent Prognostic Factor in Patients With Advanced Colorectal Cancer Treated With Cetuximab. Journal of Clinical Oncology. https://doi.org/10.1200/jco.2007.12.5906

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.