Drug intelligence / Profile preview

gefitinib + cisplatin + radiotherapy

Development stage
Unknown
Lead developer
AstraZeneca
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Oral, Intravenous, External Beam Radiation
01

Overview

Gefitinib + cisplatin + radiotherapy is a combination regimen used primarily in the treatment of locally advanced cancers, such as head and neck squamous cell carcinoma and esophageal carcinoma. Gefitinib is an oral small molecule inhibitor targeting the epidermal growth factor receptor (EGFR) tyrosine kinase, thereby blocking EGFR-mediated signaling pathways involved in tumor cell proliferation and survival. Cisplatin is a platinum-based chemotherapeutic agent that induces DNA crosslinking, leading to apoptosis of rapidly dividing cells. Radiotherapy uses ionizing radiation to damage DNA in cancer cells, further enhancing cytotoxicity. Preclinical studies have shown synergistic effects when combining these agents, with clinical trials demonstrating feasibility and tolerability for this regimen[1][2][3][4]. The combination aims to improve response rates by simultaneously inhibiting EGFR signaling, inducing DNA damage through chemotherapy, and maximizing local tumor control with radiation.

Other names
ZD1839ZD-1839ZD 1839CDDP
02

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