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Published on: February 12, 2017
High-dose-rate afterloading intraluminal brachytherapy for advanced inoperable rectal carcinoma
Carie Corner1, Linda Bryant, Caroline Chapman
1Mount Vernon Cancer Centre, Rickmansworth Road, Middlesex, United Kingdom. cariecorner@yahoo.com
Purpose:
High-dose-rate (HDR) intraluminal brachytherapy for advanced or inoperable tumors of the rectum has been used both palliatively and to dose escalate after chemoradiation for curative treatment.
Methods:
Between 1993 and 2007, 79 patients were treated with HDR afterloading brachytherapy for rectal cancer; 70 patients had adenocarcinoma of the rectum; and 9 patients had squamous cell carcinoma of the anal canal. Fifty-two patients had localized disease but were unfit for major surgery and received radiotherapy with radical intent. Twenty-seven patients with advanced or metastatic disease received palliative treatment. The median age was 82 years (range, 33-97). Radical treatment comprised either chemoradiation followed by intraluminal brachytherapy delivering 12 Gy at 1 cm in two fractions or radical monotherapy delivering up to 36 Gy at 1 cm in six fractions two to three times weekly. Palliative HDR brachytherapy schedules were predominantly 10 Gy at 1 cm single dose.
Results:
Objective local tumor response was seen in 41 of 48 assessable patients (85%); of whom, 28 patients (58%) had a complete response and 13 (27%) had a partial response. The most common symptom was rectal bleeding, which was controlled with a complete response rate of 63%. The median duration of the symptom response was 3 months (range, 1-73), and the median survival of the palliative patients was 6 months (range, 1 week-37 months). The median survival for patients treated with radical intent was 18.5 months (range, 2-119). Six patients reported late toxicity with three cases of rectal ulcer, two strictures, and one fistula.
Conclusions:
Intraluminal HDR brachytherapy is effective as local treatment in both the radical and palliative setting, with high tumor and symptom response rates, and acceptable late toxicity.

