Skip to main content
Clinical Trials/NCT05160818
NCT05160818
Recruiting
Not Applicable

Hypofractionated Stereotactic Radiotherapy Versus Single Fraction Stereotactic Radiosurgery to the Resection Cavity of Brain Metastases After Surgical Resection - A Prospective, Randomized, Controlled, Monocentric Phase III Trial

Technical University of Munich1 site in 1 country126 target enrollmentFebruary 1, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Brain Metastases
Sponsor
Technical University of Munich
Enrollment
126
Locations
1
Primary Endpoint
Local control
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

This prospective, randomized, controlled, monocentric clinical phase III study focuses on stereotactic irradiation of resection cavities of brain metastases after surgical resection and seeks to demonstrate the superiority of fractionated irradiation schemes in terms of local control.

Detailed Description

There is a growing scientific focus on single fraction stereotactic (SRS) and hypofractionated stereotactic irradiation (HFSRT) after surgical resection of brain metastasis and its use is more frequently recommended in international guidelines. Despite intensive research, the optimal fractionation scheme and dose prescription for adjuvant irradiation of the resection cavity remains unclear. Based on our own institutional data \[Cit.1\] and a recently published metaanalysis \[Cit.2\], we hypothesize that local control (LC) after HFSRT is superior compared to SRS in terms of LC. To evaluate the hypothesis in a prospective, randomized, controlled setting we designed the SATURNUS study. A total of 126 patients will be randomized 1:1 to either HFSRT (dose 6-7 x 5 Gy) or SRS (dose 1 x 12-20 Gy). If further unresected brain metastases are present, they will be treated with SRS (1 x 14 - 22 Gy). Irradiation is carried out with a Gamma Knife or a Linear Accelerator. In line with current clinical practice, the choice of positioning method for SRS with the Gamma Knife (mask or stereotactic frame) is left to the patient. In the case of SRS with the Linear Accelerator or HFSRT, fixation is done with a mask as technically not otherwise feasible. Follow-up-MRI will be at least carried out 6 weeks and 3, 6, 9 and 12 months after treatment. Primary endpoint of the study is local control (LC) at the irradiated resection cavity after 12 months. Locoregional control (LRC) and overall survival (OS) as well as salvage-treatments, irradiation-associated toxicities (especially rate of radionecrosis) and quality-of-life parameters are investigated as secondary endpoints. To the best of our knowledge, the SATURNUS study is the only randomized phase III study comparing different techniques of postoperative stereotactic radiotherapy after resection of brain metastases adequately powered to detect a superiority of HSFRT regarding LC.

Registry
clinicaltrials.gov
Start Date
February 1, 2021
End Date
August 1, 2025
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Technical University of Munich
Responsible Party
Principal Investigator
Principal Investigator

Stephanie Combs

Univ.-Prof. Dr. med. Stephanie E. Combs

Technical University of Munich

Eligibility Criteria

Inclusion Criteria

  • Histologically confirmed solid tumor disease
  • One to three resected brain metastases
  • Consent to perform adjuvant irradiation by an interdisciplinary tumor board
  • Completed wound healing
  • Resection within the last six weeks at the time of study inclusion
  • Diameter of the resection cavity ≤ 4 cm (on Planning MRI)
  • Age \> 18 years
  • KPS \> 60%
  • Adequate contraceptive measures for fertile women / men
  • Written informed consent (must be available before enrolment in the trial)

Exclusion Criteria

  • Contraindication for repetitive contrast enhanced MRI
  • Leptomeningeal disease
  • Small cell histology, hematological malignancies and / or germ cell malignancies
  • Previous irradiation of the brain
  • Pregnant and lactating women
  • Inability to understand the character and consequences of the study
  • Withdrawal of consent

Outcomes

Primary Outcomes

Local control

Time Frame: 12 months after adjuvant radiotherapy

Local control at the resected site(s)

Secondary Outcomes

  • Salvage-free survival(12 months after adjuvant radiotherapy)
  • LRC(12 months after adjuvant radiotherapy)
  • OS(12 months after adjuvant radiotherapy)
  • Irradiation-related toxicity(up to 12 months after adjuvant radiotherapy)
  • QoL(up to 12 months after adjuvant radiotherapy)
  • LC(12 months after adjuvant radiotherapy)
  • Intracranial salvage therapy(12 months after adjuvant radiotherapy)
  • Pseudoprogression(up to 12 months after adjuvant radiotherapy)
  • Time to loss of independence(up to 12 months after adjuvant radiotherapy)

Study Sites (1)

Loading locations...

Similar Trials