Abstract
Expression of epidermal growth factor and its transmembrane receptor (EGFR) stimulates tumor growth. Matuzumab is a humanized anti-EGFR monoclonal antibody that blocks EGFR activation and downstream signaling, inhibits tumor growth, and provides a clinical benefit for some patients. The plasma half-life (6-10 days) and pharmacodynamic activity allow flexible dosing on weekly, every-2-week, and every-3-week schedules. Matuzumab has shown single-agent antitumor activity in heavily pretreated patients with a variety of tumors, with a favorable safety profile. Skin rash is the most common toxicity, but is severe (Grade 3) in < 1 percent. This article describes preclinical and clinical development of matuzumab.
Original language | English (US) |
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Pages (from-to) | 81-95 |
Number of pages | 15 |
Journal | Cancer Investigation |
Volume | 26 |
Issue number | 1 |
DOIs | |
State | Published - Jan 14 2008 |
Keywords
- Anti-EGFR therapeutics
- EGFR
- Matuzumab
- Pharmacodynamics
- Pharmacokinetics
- Safety
- Tolerability
ASJC Scopus subject areas
- Oncology
- Cancer Research