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Multi-Determinants Analysis of Molecular Alterations for Predicting Clinical Benefit to EGFR-Targeted Monoclonal Antibodies in Colorectal Cancer

Overview of attention for article published in PLOS ONE, October 2009
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Title
Multi-Determinants Analysis of Molecular Alterations for Predicting Clinical Benefit to EGFR-Targeted Monoclonal Antibodies in Colorectal Cancer
Published in
PLOS ONE, October 2009
DOI 10.1371/journal.pone.0007287
Pubmed ID
Authors

Andrea Sartore-Bianchi, Federica Di Nicolantonio, Michele Nichelatti, Francesca Molinari, Sara De Dosso, Piercarlo Saletti, Miriam Martini, Tiziana Cipani, Giovanna Marrapese, Luca Mazzucchelli, Simona Lamba, Silvio Veronese, Milo Frattini, Alberto Bardelli, Salvatore Siena

Abstract

KRAS mutations occur in 35-45% of metastatic colorectal cancers (mCRC) and preclude responsiveness to EGFR-targeted therapy with cetuximab or panitumumab. However, less than 20% patients displaying wild-type KRAS tumors achieve objective response. Alterations in other effectors downstream of the EGFR, such as BRAF, and deregulation of the PIK3CA/PTEN pathway have independently been found to give rise to resistance. We present a comprehensive analysis of KRAS, BRAF, PIK3CA mutations, and PTEN expression in mCRC patients treated with cetuximab or panitumumab, with the aim of clarifying the relative contribution of these molecular alterations to resistance.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 138 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 3 2%
Netherlands 1 <1%
Ireland 1 <1%
United Kingdom 1 <1%
India 1 <1%
Spain 1 <1%
Romania 1 <1%
Unknown 129 93%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 26 19%
Researcher 23 17%
Other 14 10%
Student > Postgraduate 13 9%
Student > Master 12 9%
Other 35 25%
Unknown 15 11%
Readers by discipline Count As %
Medicine and Dentistry 55 40%
Agricultural and Biological Sciences 31 22%
Biochemistry, Genetics and Molecular Biology 13 9%
Chemistry 4 3%
Pharmacology, Toxicology and Pharmaceutical Science 3 2%
Other 10 7%
Unknown 22 16%