Paclitaxel and concurrent radiation for locally advanced pancreatic cancer.
Level II
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Abstract
To determine the activity and toxicity of paclitaxel and concurrent radiation for pancreatic cancer. Forty-four patients with locally unresectable pancreatic cancer were studied. Patients received paclitaxel, 50 mg/m(2) by 3 h i.v. (IV) infusion, weekly, on Days 1, 8, 15, 22 and 29. Radiation was administered concurrently to a total dose of 50.4 Gy, in 1.80 Gy fractions, for 28 treatments. Nausea and vomiting were the most common toxicities, Grade 3 in five patients (12%). Two patients (5%) had Grade 4 hypersensitivity reactions to their first dose of paclitaxel. Of 42 evaluable patients, the overall response rate was 26%. The median survival was 8 months, and the 1-year survival was 30%. Concurrent paclitaxel and radiation demonstrate local-regional activity in pancreatic cancer. Future investigations combining paclitaxel with other local-regional and systemic treatments are warranted.
Medical subject headings
- Antineoplastic Agents, Phytogenic
- Paclitaxel
- Pancreatic Neoplasms
- Radiation-Sensitizing Agents