A 15-Year Single-Institution Retrospective Study of Primary Pancreatic Cancer Treated with Non-Ablative Palliative Radiotherapy.

ABSTRACT

We studied the use of palliative radiotherapy (RT) among patients with primary, non-curable, locally advanced pancreatic cancer. In this subset of patients, with very poor survival, various palliative RT dose fractionation schemes are used; but, in the absence of a guideline, practice patterns vary, and dose choice is mainly based on the physician's intuition. We divided the patients into three groups, according to the dose fractionation schedules received low (A), intermediate (B), and high (C) dose groups, to study the potential differences in outcome between the different dose prescriptions. Cohort n = 184. Median age 69 years. Male n = 105 (57%), female n = 79 (43%). Stage IV n = 117 (64%). T4 n = 127 (69%). Tumor location head n = 109 (59%), body n = 37 (20%), tail n = 25 (14%), neck n = 11 (6%), and uncinate n = 2 (1%). Prior systemic therapy n = 66 (36%). Most common dose fractionations received 20 Gy in five fractions n = 67 (36%), 30 Gy in 10 fractions n = 49 (27%), and 8 Gy in one fraction n = 23 (13%). Group A n = 33 (18%), median overall survival (OS) 19 days (95% CI 4-33). Group B n = 84 (46%), median OS 52 days (95% CI 43-60). Group C n = 67 (36%), median OS 126 days (95% CI 77-174). Median days to in-field progression Group A 59 days (range 7-109), Group B 96 days (range 19-173), and Group C 97 days (range 13-475). To our knowledge, this is the largest reported retrospective cohort of patients receiving non-ablative palliative RT to treat their primary pancreatic tumors. Most patients had metastatic disease, T4 tumors of the pancreatic head and had not received prior systemic therapy. A significant survival benefit was seen favoring the high dose/longer RT fractionation group, presumably due to appropriate patient selection rather than an RT effect. Despite the relatively short median overall survival, one fifth of the patients were found to experience an in-field progression following RT.