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Trial of Neoadjuvant Intensity-Modulated Radiation Therapy Followed by Surgery and Intraoperative Radiation Therapy in Resectable Retroperitoneal Soft Tissue Sarcoma (RETRO-WTS)

Clinical Phase I/II Trial to Investigate Preoperative Dose-Escalated Intensity-Modulated Radiation Therapy (IMRT) and Intraoperative Radiation Therapy (IORT) in Patients With Retroperitoneal Soft Tissue Sarcoma

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01566123
Enrollment
37
Registered
2012-03-29
Start date
2007-03-31
Completion date
2020-02-29
Last updated
2020-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Retroperitoneal Soft Tissue Sarcoma

Keywords

retroperitoneal soft tissue sarcoma, IMRT, IORT

Brief summary

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.

Interventions

RADIATIONNeoadjuvant intensity-modulated radiation therapy (IMRT)

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

Sponsors

German Cancer Research Center
CollaboratorOTHER
University Hospital Heidelberg
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* written informed consent * histologically confirmed, primary or locally recurrent soft tissue sarcoma of the retroperitoneal space * judged as at least marginally resectable * absence of distant metastases * tumor size ≥ 5 cm

Exclusion criteria

* missing written informed consent * missing histological confirmation of soft tissue sarcoma * Desmoid tumor (syn. aggressive fibromatosis) * judged as gross incomplete or not resectable * incomplete staging * presence of distant metastases * prior radiation therapy to the abdominal region * participation in another clinical interventional study * inflammatory bowel disease

Design outcomes

Primary

MeasureTime frame
Local Control Rate5 year

Secondary

MeasureTime frameDescription
Severe acute gastrointestinal toxicityup to 3 months from first day of treatmentsevere defined as grade \>= III, scored according to CTC AE 3.0
Progression free survivalup to 5 years from first day of treatment
Overall Survivalup to five years from first day of treatment
Acute toxicityup to 3 months from first day of treatmentscored according to CTCAE 3.0
Late Toxicityup to 5 years after first day of treatmentscored according to CTCAE 3.0 and RTOG criteria

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 26, 2026