In order to reduce hospitalisation time for patients receiving postoperativ
e radiotherapy a phase I-II study of intracavity balloon brachytherapy was
instituted. An indwelling balloon catheter was implanted during the closing
phase of the initial operation. Starting on the second or third postoperat
ive day the catheter was afterloaded with a high dose rate isotope via a re
motely controlled afterloading system. The treatment consisted of 10-12 fra
ctions over a period of 5-6 days, with each treatment session requiring app
roximately 15 minutes. No external beam radiation was given.
Forty-four newly diagnosed patients were treated. A total dose of either 60
Gy (33 patients) or 72 Gy (11 patients) was given.
The overall median survival was 11.7 months, (range 2.7-50.9). The treatmen
t was well tolerated and none of the applicators were removed prematurely.
The total median hospital stay for this group of patients was significantly
reduced compared to more conventional protocols.
This study indicates that intracavity high dose rate balloon brachytherapy
can achieve survival rates equivalent to those of conventional radiotherapy
and is both cost and time efficient.