Local control rates in patients with retroperitoneal soft tissue sarcoma (RSTS) remain disappointing even after gross total resection, mainly because wide margins are not achievable in the majority of patients. In contrast to extremity sarcoma, postoperative radiation therapy (RT) has shown limited efficacy due to its limitations in achievable dose and coverage. Although Intraoperative Radiation Therapy (IORT) has been introduced in some centers to overcome these dose limitations and resulted in improved outcome, local failure rates are still high even if considerable treatment related toxicity is accepted. As postoperative administration of RT has some general disadvantages, neoadjuvant approaches could offer benefits in terms of dose escalation, target coverage and reduction of toxicity, especially if highly conformal techniques like intensity-modulated radiation therapy (IMRT) are considered. Therefore the RETROWTS trials has been designed as a prospective, one armed, single center phase I/II study investigating a combination of neoadjuvant dose-escalated IMRT (50-56 Gy) followed by surgery and IORT (10-12 Gy) in patients with at least marginally resectable RSTS. The primary objective is the local control rate after five years. Secondary endpoints are progression-free and overall survival, acute and late toxicity, surgical resectability and patterns of failure. The aim of accrual is 37 patients in the per-protocol population.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
37
neoadjuvant intensity-modulated radiation therapy, single dose 2.0-2.4 Gy, total dose 50-56 Gy
during surgery, 10-12 Gy (90% isodose) to the tumor bed or residual disease
University Hospital Heidelberg
Heidelberg, Baden-Wurttemberg, Germany
Local Control Rate
Time frame: 5 year
Progression free survival
Time frame: up to 5 years from first day of treatment
Overall Survival
Time frame: up to five years from first day of treatment
Acute toxicity
scored according to CTCAE 3.0
Time frame: up to 3 months from first day of treatment
Late Toxicity
scored according to CTCAE 3.0 and RTOG criteria
Time frame: up to 5 years after first day of treatment
Severe acute gastrointestinal toxicity
severe defined as grade \>= III, scored according to CTC AE 3.0
Time frame: up to 3 months from first day of treatment
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