Volume 70, Issue 3 , Pages 735-743, 1 March 2008
Role of Adjuvant Chemoradiation Therapy in Adenocarcinomas of the Ampulla of Vater
Purpose
The role of adjuvant chemoradiation therapy (CRT) in the treatment of ampullary cancers remains undefined. We retrospectively compared treatment outcomes in patients treated with pancreaticoduodenectomy alone versus those who received additional adjuvant CRT.
Methods and Materials
Between May 1990 and January 2006, 54 of 96 patients with ampullary adenocarcinoma who underwent potentially curative pancreaticoduodenectomy also received adjuvant CRT. The median preoperative radiation dose was 45 Gy (range, 30–50.4 Gy) and median postoperative dose was 50.4 Gy (range, 45–55.8 Gy). Concurrent chemotherapy included primarily 5-fluorouracil (52%) and capecitabine (43%). Median follow-up was 31 months. Univariate and multivariate statistical methodologies were used to determine significant prognostic factors for local control (LC), distant control (DC), and overall survival (OS).
Results
Actuarial 5-year LC, DC, and OS were 77%, 69%, and 64%, respectively. On univariate analysis, age, gender, race/ethnicity, tumor grade, use of adjuvant treatment, and sequencing of adjuvant therapy were not significantly associated with LC, DC, or OS. However, on univariate analysis, T3/T4 tumor stage was prognostic for poorer LC and OS (p = 0.02 and p < 0.001, respectively); node-positive disease was prognostic for poorer LC (p = 0.03). On multivariate analysis, T3/T4 tumor stage was independently prognostic for decreased OS (p = 0.002). Among these patients (n = 34), those who received adjuvant CRT had a trend toward improved OS (median, 35.2 vs. 16.5 months; p = 0.06).
Conclusions
Ampullary cancers have a distinctly better treatment outcome than pancreatic adenocarcinomas. Higher primary tumor stage (T3/T4), an independent adverse risk factor for poorer treatment outcomes, may warrant the addition of adjuvant CRT to pancreaticoduodenectomy.
Ampullary cancer, Adjuvant, Chemotherapy, Radiation therapy
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Presented in part at the 2006 American Society of Clinical Oncology Gastrointestinal Cancers Symposium, January 26–28, 2006, San Francisco, CA.
Conflict of interest: none.
PII: S0360-3016(07)03672-3
doi:10.1016/j.ijrobp.2007.07.2327
© 2008 Elsevier Inc. All rights reserved.
Volume 70, Issue 3 , Pages 735-743, 1 March 2008
