Between February 2001 and February 2005, 50 patients with a history of pelvic radiotherapy were treated with hyperfractionated accelerated radiotherapy for primary (n = 2 patients) or recurrent (n = 48 patients) rectal adenocarcinoma. Patients were treated with 150-cGy fractions twice daily, with a total dose of 39 Gy (n = 47 patients) if the retreatment interval was ≥1 year or 30 Gy (n = 3) if the retreatment interval was <1 year. Concurrent chemotherapy was administered to 48 (96 % ) patients. Eighteen (36 % ) patients underwent surgical resection following radiotherapy.
Two patients had grade 3 acute toxicity and 13 patients had grade 3 to 4 late toxicity. The 3-year rate of grade 3 to 4 late toxicity was 35 % . The 3-year rate of freedom from local progression was 33 % . The 3-year freedom from local progression rate was 47 % in patients undergoing surgery and 21 % in those not undergoing surgery (p = 0.057). The 3-year overall survival rate was 39 % . The 3-year overall survival rate was 66 % in patients undergoing surgery and 27 % in those not undergoing surgery (p = 0.003). The 3-year overall survival rate was 53 % in patients with a retreatment interval of >2 years and 21 % in those with a retreatment interval of ≤2 years (p = 0.001).
Hyperfractionated, accelerated reirradiation was well tolerated, with low rates of acute toxicity and moderate rates of late toxicity. Reirradiation may help improve pelvic control in rectal cancer patients with a history of pelvic radiotherapy.