Mj. Eble et al., METHODOLOGICAL APPROACHES AND POSTOPERATI VE MORBIDITY OF INTRAOPERATIVE RADIOTHERAPY FOR SOFT-TISSUE SARCOMAS, Radiologe, 33(9), 1993, pp. 513-519
Since June 1991 the IORT facility has operated a dedicated linear acce
lerator, which was installed within the central operating theater of t
he Department of Surgery. As of 9/92 a total of 28 patients suffering
from peripheral (n = 20) or centrally (n = 8) located soft tissue sarc
omas had been were treated. Thirteen patients revealed a primary and 1
5 patients a recurrent tumor. Tumor resection with negative margins wa
s performed in 20 patients, positive margins remained in 5 patients, a
nd gross macroscopic residual disease in 3 patients. Combined intraope
rative and external beam radiotherapy was applied in 22 patients, usin
g IORT doses of 10-20 Gy and an external beam dose of 26-50 Gy. Three
patients were irradiated intraoperatively twice with a time interval o
f 24 h. After a median follow-up of 9.9 months, 20 patients are diseas
e free. Two patients died 4 and 5 months after the end of therapy with
rapidly progressive distant metastases. An in-field failure within th
e external beam target volume was seen in 1 patient and local failure
at the field margin of the external field in 3 patients. So far, there
have been no IORT infield failures. Follow-up is performed with magne
tic resonance imaging. In 3 patients a second operation was necessary
because of a severe wound infection, including one patient suffering f
rom osteomyelitis of a neighboring bone. Mild sensory neuropathy occur
red in 1 patient 7 months after treatment. Overall only mild and rever
sible postoperative and posttherapeutic complications were seen. Based
on the retrospective analysis of the target volumes chosen during thi
s working period, a set of horse-shoe-shaped cones was designed, which
permitted circular and longitudinal target volumes with a homogeneous
doses to be delivered as well. With this dedicated IORT facility simp
le and safe application of a high boost dose is possible. To improve l
ocal tumor control in soft tissue sarcomas further, a clear definition
of the target volume, followed by an exact verification and at least
integration of this target volume in a three-dimensional treatment pla
n, is necessary.