Combined chemoradiotherapy for unresectable pancreatic cancer

Citation
Jl. Martin et al., Combined chemoradiotherapy for unresectable pancreatic cancer, AM J CL ONC, 22(3), 1999, pp. 309-314
Citations number
27
Categorie Soggetti
Oncology
Journal title
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS
ISSN journal
02773732 → ACNP
Volume
22
Issue
3
Year of publication
1999
Pages
309 - 314
Database
ISI
SICI code
0277-3732(199906)22:3<309:CCFUPC>2.0.ZU;2-I
Abstract
This study was undertaken to evaluate the efficacy of a regimen of combined chemoradiotherapy in patients with unresectable adenocarcinoma of the panc reas. An analysis was undertaken on 27 patients from January 1992 to May 19 96. Patients had a median age of 70 years (range, 40-78) and Eastern Cooper ative Oncology Group Performance Status of 0-2. Eighteen patients had locor egional disease (T-2-T-3, N-0-N-1, M-0), and nine had metastatic disease. C hemotherapy consisted of four cycles of 5-fluorouracil 1 gm/m(2)/day as a c ontinuous infusion over 110 hours, streptozotocin 300 mg/m(2)/day over 30 m inutes on days 2-4, and cisplatin 100 mg/m(2) over 2 hours on day 4 only, f ollowed by a maintenance regimen of 5-fluorouracil and leucovorin every 2 w eeks. The radiotherapy was administered as a split course concurrently with chemotherapy to a total dose of 6000 cGy. Toxicity was frequent, but there were no treatment-related deaths. Grade III and IV toxicity was primarily limited to myelosuppression, stomatitis, and gastrointestinal side effects. Fifteen patients (56%) were able to complete either three or four cycles o f chemoradiotherapy. All patients were evaluable for toxicity, response, an d survival. Nine patients (33%) had an objective response (four complete re sponse 5 partial response), two remained stable, and 16 (59%) had disease p rogression. Median survival for the entire group was 19 weeks (2-139), and the median survival for overall responders was 56 weeks (15-139), No patien t with localized disease underwent subsequent surgical resection. The autho rs conclude that those patients who are able to tolerate the entire treatme nt regimen may achieve a useful prolongation of time to tumor progression.