4.4 Article

Response to erlotinib in a patient with treatment refractory chordoma

Journal

ANTI-CANCER DRUGS
Volume 20, Issue 10, Pages 953-955

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/CAD.0b013e328330c7f0

Keywords

chordoma; epidermal growth factor receptor; epidermal growth factor receptor tyrosine kinase inhibitors; erlotinib; imatinib

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Chordomas are rare tumors arising from the axial skeleton. The disease is characterized by slow local growth, frequent local recurrences, and rare systemic spread. Surgery and local radiation remains the mainstay of treatment with minimal role of systemic therapy. Imatinib has been shown to be active in a phase 11 trial with symptomatic and radiological responses. We report a case where treatment with erlotinib, an epidermal growth factor receptor tyrosine kinase inhibitor, induced symptomatic and radiological response in a patient with disease refractory to imatinib and vascular disrupting agent Anti-Cancer Drugs 20:953-955 (C) 2009 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.

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