Cetuximab Shows Activity in Colorectal Cancer Patients With Tumors That Do Not Express the Epidermal Growth Factor Receptor by Immunohistochemistry
Top Cited Papers
- 20 March 2005
- journal article
- gastrointestinal cancer
- Published by American Society of Clinical Oncology (ASCO) in Journal of Clinical Oncology
- Vol. 23 (9) , 1803-1810
- https://doi.org/10.1200/jco.2005.08.037
Abstract
Purpose: To establish evidence of activity, or lack thereof, of cetuximab-based therapy in patients with refractory colorectal cancer with tumors that do not demonstrate epidermal growth factor receptor (EGFR) expression by immunohistochemistry (IHC). Patients and Methods: Pharmacy computer records were reviewed to identify all patients who received cetuximab at Memorial Sloan-Kettering Cancer Center in a nonstudy setting during the first 3 months of cetuximab's commercial availability. Medical records of these patients were then reviewed to identify colorectal cancer patients who had experienced failure with a prior irinotecan-based regimen and who had a pathology report indicating an EGFR-negative tumor by IHC. Pathology slides from these patients were reviewed by a reference pathologist to confirm EGFR negativity, and computed tomography scans during cetuximab-based therapy were reviewed by a reference radiologist. Response rates were reported using WHO criteria. Results: Sixteen chemotherapy-refractory, EGFR-negative colorectal cancer patients who received cetuximab in a nonstudy setting were identified. Fourteen of these patients received cetuximab plus irinotecan, and two received cetuximab monotherapy. In the 16 patients, four major objective responses were seen (response rate, 25%; 95% CI, 4% to 46%). Conclusion: Colorectal cancer patients with EGFR-negative tumors have the potential to respond to cetuximab-based therapies. EGFR analysis by current IHC techniques does not seem to have predictive value, and selection or exclusion of patients for cetuximab therapy on the basis of currently available EGFR IHC does not seem warranted.Keywords
This publication has 22 references indexed in Scilit:
- Identification of the Epitope for the Epidermal Growth Factor Receptor-specific Monoclonal Antibody 806 Reveals That It Preferentially Recognizes an Untethered Form of the ReceptorJournal of Biological Chemistry, 2004
- Immunohistochemical Detection of EGFR in Paraffin-embedded Tumor TissuesJournal of Histochemistry & Cytochemistry, 2004
- Pharmacokinetic and pharmacodynamic properties of EGFR inhibitors under clinical investigationCancer Treatment Reviews, 2004
- Phase II Trial of Cetuximab in Patients With Refractory Colorectal Cancer That Expresses the Epidermal Growth Factor ReceptorJournal of Clinical Oncology, 2004
- Epidermal Growth Factor Receptor in Vulvar Malignancies and Its Relationship to Metastasis and Patient SurvivalGynecologic Oncology, 1997
- Thermal Inactivation of the Protein Tyrosine Kinase of the Epidermal Growth Factor ReceptorBiochemistry, 1996
- Differential heat stress stability of epidermal growth factor receptor and erbB‐2 receptor tyrosine kinase activitiesJournal of Cellular Physiology, 1993
- High-affinity epidermal growth factor binding is specifically reduced by a monoclonal antibody, and appears necessary for early responses.The Journal of cell biology, 1990
- Signal transduction by epidermal growth factor occurs through the subclass of high affinity receptors.The Journal of cell biology, 1989
- A431 cell variants lacking the blood group A antigen display increased high affinity epidermal growth factor-receptor number, protein-tyrosine kinase activity, and receptor turnover.The Journal of cell biology, 1988