Brain Metastases, Resection Cavity
Conditions
Keywords
Brain Metastases, Resection Cavity, Radiotherapy, Stereotactic Irradiation, Gamma Knife
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.
Interventions
RADIATIONHypofractionated stereotactic radiotherapy (HFSRT) versus single fraction stereotactic radiotherapy radiosurgery (SRS)
intervention description see above
Sponsors
Technical University of Munich
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Masking description
The affiliation to the treatment arm will not be blinded to anyone except the study neuroradiologist.
Intervention model description
1:1 Parallel Assignment
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Local control | 12 months after adjuvant radiotherapy | Local control at the resected site(s) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| QoL | up to 12 months after adjuvant radiotherapy | Quality of life according to EORTC QLQ-C30 and EORTC QLQ-B20 |
| Irradiation-related toxicity | up to 12 months after adjuvant radiotherapy | according to CTCAE v4.03, especially rate of radionecrosis |
| LC | 12 months after adjuvant radiotherapy | Local control at all treated site(s) |
| LRC | 12 months after adjuvant radiotherapy | Locoregional control=CNS progression free survival |
| Pseudoprogression | up to 12 months after adjuvant radiotherapy | Rate of pseudoprogression |
| Salvage-free survival | 12 months after adjuvant radiotherapy | Overall survival |
| Intracranial salvage therapy | 12 months after adjuvant radiotherapy | Number and kind of intracranial salvage treatments |
| Time to loss of independence | up to 12 months after adjuvant radiotherapy | defined as decrease in Barthel index by \> 20 points |
| OS | 12 months after adjuvant radiotherapy | Overall survival |
Countries
Germany
Contacts
Primary ContactMaria Waltenberger
Backup ContactStephanie E Combs, Prof. Dr.
Outcome results
None listed