SATURNUS: Hypofractionated Versus Single Fraction Stereotactic Adjuvant Radiotherapy to the Resection Cavity of Brain Metastases

Sponsor
Technische Universität München (Other)
Overall Status
Recruiting
CT.gov ID
NCT05160818
Collaborator
(none)
126
1
2
53.9
2.3

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Radiation: Hypofractionated stereotactic radiotherapy (HFSRT) versus single fraction stereotactic radiotherapy radiosurgery (SRS)
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
126 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
1:1 Parallel Assignment1:1 Parallel Assignment
Masking:
None (Open Label)
Masking Description:
The affiliation to the treatment arm will not be blinded to anyone except the study neuroradiologist.
Primary Purpose:
Treatment
Official Title:
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
Actual Study Start Date :
Feb 1, 2021
Anticipated Primary Completion Date :
Aug 1, 2025
Anticipated Study Completion Date :
Aug 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Arm A: HSFRT

Hypofractionated stereotactic radiotherapy to the resection cavity, dose prescription: 6-7 x 5 Gy

Radiation: Hypofractionated stereotactic radiotherapy (HFSRT) versus single fraction stereotactic radiotherapy radiosurgery (SRS)
intervention description see above

Active Comparator: Arm B: SRS

Single fraction stereotactic radiotherapy to the resection cavity, dose prescription: 1 x 12-20 Gy

Radiation: Hypofractionated stereotactic radiotherapy (HFSRT) versus single fraction stereotactic radiotherapy radiosurgery (SRS)
intervention description see above

Outcome Measures

Primary Outcome Measures

  1. Local control [12 months after adjuvant radiotherapy]

    Local control at the resected site(s)

Secondary Outcome Measures

  1. LC [12 months after adjuvant radiotherapy]

    Local control at all treated site(s)

  2. LRC [12 months after adjuvant radiotherapy]

    Locoregional control=CNS progression free survival

  3. OS [12 months after adjuvant radiotherapy]

    Overall survival

  4. Salvage-free survival [12 months after adjuvant radiotherapy]

    Overall survival

  5. Intracranial salvage therapy [12 months after adjuvant radiotherapy]

    Number and kind of intracranial salvage treatments

  6. Pseudoprogression [up to 12 months after adjuvant radiotherapy]

    Rate of pseudoprogression

  7. Irradiation-related toxicity [up to 12 months after adjuvant radiotherapy]

    according to CTCAE v4.03, especially rate of radionecrosis

  8. QoL [up to 12 months after adjuvant radiotherapy]

    Quality of life according to EORTC QLQ-C30 and EORTC QLQ-B20

  9. Time to loss of independence [up to 12 months after adjuvant radiotherapy]

    defined as decrease in Barthel index by > 20 points

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Dept. Radiation Oncology Munich Bavaria Germany 81675

Sponsors and Collaborators

  • Technische Universität München

Investigators

  • Study Director: Maria Waltenberger, Technical University Munich, Germany

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Stephanie Combs, Univ.-Prof. Dr. med. Stephanie E. Combs, Technische Universität München
ClinicalTrials.gov Identifier:
NCT05160818
Other Study ID Numbers:
  • RadOnc MRI TUM - 2
First Posted:
Dec 16, 2021
Last Update Posted:
Dec 16, 2021
Last Verified:
Dec 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Stephanie Combs, Univ.-Prof. Dr. med. Stephanie E. Combs, Technische Universität München
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 16, 2021