Paclitaxel and concurrent radiation for locally advanced pancreatic and gastric cancer: a phase I study

To determine the maximum-tolerated dose (MTD), dose-limiting toxicities, and potential antitumor activity of weekly paclitaxel with concurrent radiation (RT) for locally advanced pancreatic and gastric cancer. Thirty-four patients with locally advanced adenocarcinoma of the pancreas or stomach were...

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Published inJournal of clinical oncology Vol. 15; no. 3; p. 901
Main Authors Safran, H, King, T P, Choy, H, Hesketh, P J, Wolf, B, Altenhein, E, Sikov, W, Rosmarin, A, Akerley, W, Radie-Keane, K, Cicchetti, G, Lopez, F, Bland, K, Wanebo, H J
Format Journal Article
LanguageEnglish
Published United States 01.03.1997
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Summary:To determine the maximum-tolerated dose (MTD), dose-limiting toxicities, and potential antitumor activity of weekly paclitaxel with concurrent radiation (RT) for locally advanced pancreatic and gastric cancer. Thirty-four patients with locally advanced adenocarcinoma of the pancreas or stomach were studied. The initial dose of paclitaxel was 30 mg/m2 by 3-hour intravenous (I.V.) infusion repeated every week for 6 weeks with 50 Gy RT. Doses were escalated at 10-mg/m2 increments in successive cohorts of three new patients until dose-limiting toxicity was observed. The dose-limiting toxicities at 60 mg/m2/wk were abdominal pain within the RT field, nausea, and anorexia. Of 23 patients with assessable disease, 11 (seven with gastric, four with pancreatic cancer) had objective responses for an overall response rate of 48%. Concurrent paclitaxel with upper abdominal RT is well tolerated at dosages that have substantial activity. A phase II trial of neoadjuvant paclitaxel and RT at the MTD of 50 mg/m2/wk is underway.
ISSN:0732-183X
DOI:10.1200/JCO.1997.15.3.901