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Epidermal growth factor receptor mutation and diverse tumors: case report and concise literature review.

Abstract
We document an EGFR mutation in a patient with papillary renal cell cancer with a history of multiple therapies, including interferon-alpha, interleukin-2, 5-fluorouracil, and interferon-alpha together with 13-cis-retinoic acid, to which floxuridine was later added, and thalidomide maintenance therapy for six years. We provide a succinct review of the PubMed-derived literature on EGFR mutations in diverse tumors, which indicates that a subset of patients with various tumor types may harbor EGFR mutations. A 32-year old woman with sporadic, metastatic papillary renal cancer was found to harbor an EGFR kinase domain mutation in addition to the MET kinase mutation typically found in this disease. Since lung cancer patients with EGFR mutations often respond well to EGFR inhibitor therapy and EGFR mutations occur in a variety of tumors, it should be worthwhile to assess EGFR status prospectively in other tumors and study the results of treatment with EGFR inhibitors in these patients.
AuthorsLakshmi Chintala, Razelle Kurzrock
JournalMolecular oncology (Mol Oncol) Vol. 4 Issue 4 Pg. 306-8 (Aug 2010) ISSN: 1878-0261 [Electronic] United States
PMID20346742 (Publication Type: Case Reports, Journal Article, Review)
Copyright(c) 2010 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
Chemical References
  • ErbB Receptors
Topics
  • Adult
  • Carcinoma, Renal Cell (genetics, pathology, therapy)
  • ErbB Receptors (genetics, metabolism)
  • Female
  • Humans
  • Kidney Neoplasms (genetics, pathology, therapy)
  • Mutation

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