Oncotarget

Research Papers:

Cetuximab response in CRC patient-derived xenografts seems predicted by an expression based RAS pathway signature

Sheng Guo, Dawei Chen, Xuesong Huang, Jie Cai, Jean-Pierre Wery and Qi-Xiang Li _

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Oncotarget. 2016; 7:50575-50581. https://doi.org/10.18632/oncotarget.10499

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Abstract

Sheng Guo1, Dawei Chen1, Xuesong Huang1, Jie Cai1, Jean-Pierre Wery1, Qi-Xiang Li1,2

1Division of Translational Oncology, Crown Bioscience, Inc., Santa Clara, CA 95054, USA

2State Key Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing, 100191, China

Correspondence to:

Qi-Xiang Li, email: henryli@crownbio.com

Keywords: PDX, Erbitux, expression signature, patient stratification, biomarker

Received: December 10, 2015     Accepted: June 29, 2016     Published: July 8, 2016

ABSTRACT

Cetuximab is an approved treatment for metastatic colorectal carcinoma (mCRC) with codon 12/13-KRAS mutations, recently questioned for its validity, and alternative mutation-based biomarkers were proposed. We set out to investigate whether an expression signature can also predict response by utilizing a cetuximab mouse clinical trial (MCT) dataset on a cohort of 25 randomly selected EGFR+ CRC patient-derived xenografts (PDXs). While we found that the expression of EGFR and its ligands are not predictive of the cetuximab response, we tested a published RAS pathway signature, a 147-gene expression signature proposed to describe RAS pathway activity, against this MCT dataset. Interestingly, our study showed that the observed cetuximab activity has a strong correlation with the RAS pathway signature score, which was also demonstrated to have a certain degree of correlation with a historic clinical dataset. Altogether, the independent validations in unrelated datasets from independent cohort of CRCs strongly suggest that RAS pathway signature may be a relevant expression signature predictive of CRC response to cetuximab. Our data seem to suggest that an mRNA expressing signature may also be developed as a predictive biomarker for drug response, similarly to genetic mutations.


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