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Updated: May 28, 2026

Development and Maintenance of a Preclinical Patient Derived Tumor Xenograft Model for the Investigation of Novel Anti-Cancer Therapies
Published on: September 30, 2016
Epidermal growth factor receptor pathway mutations and colorectal cancer therapy
Allie H Grossmann1, Wade S Samowitz
1Department of Pathology, University of Utah Health Sciences Center, Salt Lake City, UT 84108, USA. wade.samowitz@aruplab.com
Context:
Rational anticancer therapy is beginning to expand the practice of surgical pathology beyond a primarily morphologic and immunophenotypic analysis into the molecular arena. Molecular testing of tumors can have both diagnostic and therapeutic value, which guides treatment decisions. This is true for colorectal cancer in which mutations in signaling mediators predict resistance to anti-epidermal growth factor receptor (anti-EGFR) therapy.
Objective:
To review the clinically relevant mutations that currently guide treatment decisions in metastatic colorectal cancer, summarize additional mutations that are expected to improve the prognostic sensitivity of molecular testing, and provide practical suggestions for submitting specimens for molecular analysis.
Data Sources:
Peer-reviewed literature reporting pertinent clinical trial data, mutation analysis, and molecular mechanisms of drug resistance, as well as comprehensive review articles germane to the topic and published testing recommendations from the College of American Pathologists.
Conclusions:
Molecular analysis of colorectal cancer is now mandated before initiation of anti-EGFR therapy and directly impacts treatment options and outcomes. Familiarity with the mutations that determine utility and efficacy of therapy, as well as the importance of careful sample selection, will facilitate appropriate testing and optimize patient care.
Insights
Molecular testing for colorectal cancer mutations is essential for guiding anti-epidermal growth factor receptor (anti-EGFR) therapy. Understanding these genetic alterations optimizes treatment selection and patient outcomes.
Area of Science:
- Oncology
- Molecular Pathology
- Genomics
Background:
- Anticancer therapy is increasingly incorporating molecular analysis alongside traditional methods.
- Molecular tumor testing provides diagnostic and therapeutic insights, crucial for personalized medicine.
- Specific mutations in colorectal cancer predict resistance to anti-epidermal growth factor receptor (anti-EGFR) therapy.
Purpose of the Study:
- To review key mutations influencing metastatic colorectal cancer treatment decisions.
- To identify emerging mutations for enhanced prognostic accuracy.
- To offer practical guidance on specimen submission for molecular analysis.
Main Methods:
- Systematic review of peer-reviewed literature on clinical trials and mutation analysis.
- Analysis of molecular mechanisms of drug resistance.
- Inclusion of comprehensive review articles and College of American Pathologists testing recommendations.
Main Results:
- Molecular analysis of colorectal cancer is now a prerequisite for anti-EGFR therapy.
- Identified mutations directly impact treatment choices and patient prognosis.
- Understanding specific mutations is vital for predicting therapy efficacy.
Conclusions:
- Mandatory molecular testing for colorectal cancer is critical before anti-EGFR therapy.
- Knowledge of predictive mutations enhances treatment selection and patient outcomes.
- Careful specimen selection and molecular analysis optimize patient care.
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