Background
While adjuvant chemoradiation is commonly used in the United States for treatment of resected pancreatic cancer, there is no consensus on the benefit of this therapy as results from randomized trials are conflicting. We reviewed our experience in a consecutive, unselected series of patients treated with adjuvant 5-FU and radiation therapy for resected pancreatic adenocarcinoma.
Methods
86 patients with resected pancreatic adenocarcinoma who underwent adjuvant therapy from 1998–2005 were identified. Medical records were reviewed. 93% of patients were treated with external beam RT to ≥ 50.4 Gy and 91% of patients received concurrent 5-FU by continuous infusion. 45% of patients went on to receive adjuvant gemcitabine.
Results
Median follow-up was 31 months (range 21–62) among the 20 patients still alive. Fewer than half of patients had positive (33%) or close (<1mm, 15%) resection margins. 81% of the tumors were T3; 66% had involved lymph nodes. The median overall survival (OS) for all patients was 22 months; negative lymph node status (p=0.016) was a significant prognostic factor for improved OS, while treatment with gemcitabine trended towards improved OS (p=0.080). Median disease-free survival (DFS) for all patients was 10 months, and treatment with gemcitabine (p=0.044) or any chemotherapy (p=0.047) were significant predictors of DFS. 75 patients (87%) had disease recurrence, the majority of whom recurred with peritoneal (55%) or liver (53%) metastases. Negative lymph nodes trended towards a lower rate of distant failure (p=0.060).
Conclusions
The median survival of this cohort is greater than that of the chemoradiation arms of the EORTC and ESPAC-1 trials, and comparable to the survival observed on the GITSG chemoradiation arm. Lymph node status and treatment with adjuvant chemotherapy were significant predictors of OS and DFS, respectively. Future survival improvements should be directed at reducing peritoneal and liver metastases. Further randomized trials are required to define the role of adjuvant therapy for pancreatic adenocarcinoma.