Gemcitabine chemotherapy and single-fraction stereotactic body radiotherapy for locally advanced pancreatic cancer Journal Article


Authors: Schellenberg, D.; Goodman, K. A.; Lee, F.; Chang, S.; Kuo, T.; Ford, J. M.; Fisher, G. A.; Quon, A.; Desser, T. S.; Norton, J.; Greco, R.; Yang, G. P.; Koong, A. C.
Article Title: Gemcitabine chemotherapy and single-fraction stereotactic body radiotherapy for locally advanced pancreatic cancer
Abstract: Purpose: Fractionated radiotherapy and chemotherapy for locally advanced pancreatic cancer achieves only modest local control. This prospective trial evaluated the efficacy of a single fraction of 25 Gy stereotactic body radiotherapy (SBRT) delivered between Cycle 1 and 2 of gemcitabine chemotherapy. Methods and Materials: A total of 16 patients with locally advanced, nonmetastatic, pancreatic adenocarcinoma received gemcitabine with SBRT delivered 2 weeks after completion of the first cycle. Gemcitabine was resumed 2 weeks after SBRT and was continued until progression or dose-limiting toxicity. The gross tumor volume, with a 2-3-mm margin, was treated in a single 25-Gy fraction by Cyberknife. Patients were evaluated at 4-6 weeks, 10-12 weeks, and every 3 months after SBRT. Results: All 16 patients completed SBRT. A median of four cycles (range one to nine) of chemotherapy was delivered. Three patients (19%) developed local disease progression at 14, 16, and 21 months after SBRT. The median survival was 11.4 months, with 50% of patients alive at 1 year. Patients with normal carbohydrate antigen (CA)19-9 levels either at diagnosis or after Cyberknife SBRT had longer survival (p <0.01). Acute gastrointestinal toxicity was mild, with 2 cases of Grade 2 (13%) and 1 of Grade 3 (6%) toxicity. Late gastrointestinal toxicity was more common, with five ulcers (Grade 2), one duodenal stenosis (Grade 3), and one duodenal perforation (Grade 4). A trend toward increased duodenal volumes radiated was observed in those experiencing late effects (p = 0.13). Conclusion: SBRT with gemcitabine resulted in comparable survival to conventional chemoradiotherapy and good local control. However, the rate of duodenal ulcer development was significant. © 2008 Elsevier Inc. All rights reserved.
Keywords: cancer survival; clinical article; controlled study; survival analysis; cancer recurrence; cancer growth; antineoplastic agents; gemcitabine; cancer radiotherapy; pancreas cancer; radiation dose; combined modality therapy; pancreatic neoplasms; chemotherapy; adenocarcinoma; tumor volume; radiotherapy dosage; radiotherapy; biotechnology; late effects; survivors; disease progression; stomach ulcer; radiosurgery; pancreatic adenocarcinoma; local control; pancreatic cancer; stereotactic body radiotherapy; duodenum stenosis; toxicity; deoxycytidine; carbohydrates; carbohydrate antigen; median survival; chemoradiotherapy; cyberknife; gastrointestinal diseases; gross tumor volume; organic compounds; image guided radiotherapy; pancreatic cancers; duodenum perforation; electrotherapeutics; disease progressions; dose-limiting toxicity; duodenal ulcers; first cycle; four cycles; fractionated radiotherapy; gastrointestinal toxicities
Journal Title: International Journal of Radiation Oncology, Biology, Physics
Volume: 72
Issue: 3
ISSN: 0360-3016
Publisher: Elsevier Inc.  
Date Published: 2008-11-01
Start Page: 678
End Page: 686
Language: English
DOI: 10.1016/j.ijrobp.2008.01.051
PUBMED: 18395362
PROVIDER: scopus
DOI/URL:
Notes: --- - "Cited By (since 1996): 43" - "Export Date: 17 November 2011" - "CODEN: IOBPD" - "Source: Scopus"
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  1. Karyn A Goodman
    257 Goodman