Combined radiotherapy and chemotherapy (cisplatin and 5-fluorouracil) as palliative treatment for localized unresectable or adjuvant treatment for resected pancreatic adenocarcinoma: Results of a feasibility study

Citation
T. Andre et al., Combined radiotherapy and chemotherapy (cisplatin and 5-fluorouracil) as palliative treatment for localized unresectable or adjuvant treatment for resected pancreatic adenocarcinoma: Results of a feasibility study, INT J RAD O, 46(4), 2000, pp. 903-911
Citations number
35
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Onconogenesis & Cancer Research
Journal title
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS
ISSN journal
03603016 → ACNP
Volume
46
Issue
4
Year of publication
2000
Pages
903 - 911
Database
ISI
SICI code
0360-3016(20000301)46:4<903:CRAC(A>2.0.ZU;2-1
Abstract
Purpose: To evaluate a cisplatin-containing chemoradiotherapy (CRT) regimen followed by chemotherapy for unresectable (locally advanced group, n = 32) and resected (adjuvant group, n = 10) pancreatic adenocarcinoma. The quali ty of palliation and percentage of secondary resections were also studied f or unresectable disease. Methods and Materials: The protocol comprised CRT (45 Gy over 5 weeks), com bined with 5-fluorouracil and cisplatin during the first and fifth weeks, f ollowed, 3 weeks later, by 4 cycles of the same chemotherapy plus leucovori n. Results: All patients completed CRT but only 50% of each group finished the entire protocol. Gastrointestinal toxicity and weight loss were the major side effects during CRT. Enhanced hematological toxicity limited the post-C RT chemotherapy. For the locally advanced group, median survival was 9 mont hs; 1- and 2-year survival rates were 31 and 12.5%, respectively. The overa ll response rate was 16% and 50% had stable disease. A lasting palliative e ffect defined as improved performance status and decreased analgesic consum ption, was recorded for 43% of the patients. Only three secondary resection s have been performed. For the adjuvant group, median survival was 17 month s. Conclusions: Although toxic in advanced disease, this regimen significantly lowered pain and analgesic consumption, but had poor impact on secondary r esectability. In an adjuvant setting, although equally toxic, this series w as too small to allow conclusions to be drawn. (C) 2000 Elsevier Science In c.