Phase I Trial of Gefitinib in Combination With Radiation or Chemoradiation for Patients With Locally Advanced Squamous Cell Head and Neck Cancer
| Autor: | Madeleine A. Kane, Anna E. Barón, Changhu Chen, Louis C. Harrison, David Raben, Kenneth S. Hu, John I. Song, John Campana, Sherif Said, S. Gail Eckhardt, Harry Quon, Adam Raben, Janet Dancey |
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| Rok vydání: | 2007 |
| Předmět: |
Adult
Male Oncology Cancer Research medicine.medical_specialty medicine.medical_treatment Antineoplastic Agents Gefitinib Internal medicine medicine Humans Epidermal growth factor receptor Aged Chemotherapy biology business.industry Head and neck cancer Middle Aged medicine.disease Combined Modality Therapy Surgery Radiation therapy Epidermoid carcinoma Head and Neck Neoplasms Cohort Carcinoma Squamous Cell Quinazolines biology.protein Female Cisplatin business Chemoradiotherapy medicine.drug |
| Zdroj: | Journal of Clinical Oncology. 25:4880-4886 |
| ISSN: | 1527-7755 0732-183X |
| DOI: | 10.1200/jco.2007.12.9650 |
| Popis: | Purpose To establish the safety and toxicity profile of daily gefitinib with radiation alone or with concurrent chemoradiotherapy in previously untreated patients with locally advanced squamous cell head and neck cancer (LAHNC). Patients and Methods Patients with intermediate-stage LAHNC were treated with concomitant boost radiation (RT) alone with escalating doses of daily gefitinib (250 or 500 mg; cohort I). Once a safety profile was determined with RT alone, patients with high-risk disease were then treated with daily gefitinib (250 or 500 mg), weekly cisplatin (CDDP; 30 mg/m2), and once-daily RT (cohort II). Patients also received post-RT gefitinib at 250 mg daily for a period of up to 2 years. Results Twenty-three patients were enrolled and assessable for toxicity. No dose-limiting toxicities (DLTs) were observed in patients treated in cohort I at either 250 or 500 mg of gefitinib daily with concomitant boost RT to 72 Gy. In patients receiving chemoradiotherapy and gefitinib (cohort II), DLTs included one grade 4 diarrhea and one grade 4 neutropenic fever. Fifteen patients started maintenance gefitinib, and eight (53%) experienced grade 1 to 2 acne-like skin rash and diarrhea, but no grade 3 or 4 toxicity occurred. Conclusion Gefitinib (250 or 500 mg daily) was well tolerated with concomitant boost RT or concurrent chemoradiotherapy with weekly CDDP. Protracted administration of gefitinib for up to 2 years at 250 mg daily was also tolerated well. |
| Databáze: | OpenAIRE |
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