Dose-staged Gamma Knife Radiosurgery Versus Microsurgical Resection

Sponsor
Medical University of Vienna (Other)
Overall Status
Recruiting
CT.gov ID
NCT04857905
Collaborator
(none)
100
1
2
41
2.4

Study Details

Study Description

Brief Summary

Background. Brain metastases (BM) are the most common intracranial tumor and occur in 20-40% of all oncological patients. The most common primary cancer in brain metastases is lung cancer, followed by melanoma, breast cancer, renal cancer and colorectal cancer. The incidence of brain metastases has been increasing but the occurrence of brain metastases is still associated with high morbidity and poor prognosis. The main treatment methods are stereotactic radiosurgery (SRS), microsurgical resection and whole brain irradiation (WBRT). In contrast to microsurgical resection, Gamma Knife radiosurgery (GKRS) is a non-invasive neurosurgical method, which allows treatment in multimorbid patients with contraindications for surgery in general anesthesia. Furthermore, stereotactic radiosurgery is the only local treatment method for multiple disseminated and thereby non-resectable brain metastases. In general, microsurgical resection is considered the treatment of choice for BM exceeding >3 cm in diameter. However, since the establishment of the dose-staged technique, larger metastases can also be treated radiosurgically in selected patients. This novel method allows the application of high cumulative dose for the treatment of complex brain metastases.

Aim. The aim of the study is to evaluate the clinical outcome in brain metastases patients with tumor volume between 8 and 20 ccm3. The clinical outcome will be compared between surgically and radiosurgically treated BM patients.

Patients and methods. The investigators plan to conduct an explorative prospective study including about 50 radiosurgically and 50 surgically treated patients with brain metastases. If a patient fulfill study-relevant inclusion criteria at the time of BM diagnosis, the principle study investigator will offer both treatment options to the patient. Depending on patient's choice, he/she will be categorized either to surgical or to radiosurgical treatment group. For the outcome evaluation of the different treatment options, a comprehensive database will be established. The study participations will not interfere with any clincally indicated therapeutic decisions and the study participants will not be exposed to any additional risks since both treatments represent suitable therapy options.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Microsurgical resection
  • Procedure: Gamma Knife radiosurgery
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Dose-staged Gamma Knife Radiosurgery Versus Microsurgical Resection - Evaluation of Neurosurgical Treatment Methods for Patients With Larger Brain Metastases - an Explorative Prospective Study
Actual Study Start Date :
Jul 1, 2020
Anticipated Primary Completion Date :
Jul 1, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Other: Microsurgical Resection of larger Brain Metastasis

Patients over 18 years and under 90 years Patients with KPS ≥70 Patients with NSCLC, melanoma, breast cancer or renal cancer as primary tumor Maximum of three brain metastases on the diagnostic MRI Tumor volume of 8-20 ccm3 on the diagnostic MRI Lobular brain metastases Patients without any contraindications for both treatment options Written, signed informed consent for study particaption after counseling -> Patients who after counseling decide for microsurgical resection of their brain metastasis

Procedure: Microsurgical resection
Depending on the patient's choice, the microsurgical resection of the brain metastases will be performed.

Other: Radiosurgery of larger Brain Metastasis

Patients over 18 years and under 90 years Patients with KPS ≥70 Patients with NSCLC, melanoma, breast cancer or renal cancer as primary tumor Maximum of three brain metastases on the diagnostic MRI Tumor volume of 8-20 ccm3 on the diagnostic MRI Lobular brain metastases Patients without any contraindications for both treatment options Written, signed informed consent for study particaption after study counseling -> Patients who after counseling decide for dose-staged radiosurgical treatment of their brain metastasis

Procedure: Gamma Knife radiosurgery
Depending on the patient's choice, the radiosurgical treatment of the brain metastases will be performed.

Outcome Measures

Primary Outcome Measures

  1. Overall survival [Through completion of the study, an average of 1 year]

    Time from first treatment

Secondary Outcome Measures

  1. Local tumor progression [Through completion of the study, an average of half a year]

    Time from first treatment until local tumor progression

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients over 18 years and under 90 years

  • Patients with KPS ≥70

  • Patients with NSCLC, melanoma, breast cancer or renal cancer as primary tumor

  • Maximum of three brain metastases on the diagnostic MRI

  • Tumor volume of 8-20 ccm3 on the diagnostic MRI

  • Lobular brain metastases

  • Patients without any contraindications for both treatment options

  • Written, signed informed consent for study particaption after study explanation

Exclusion Criteria:
  • Patients under 18 years and over 90 years

  • Patients with KPS <70

  • Patients with other primary tumor

  • More than three brain metastases on the diagnostic MRI

  • Tumor volume <8 or >20 ccm3 on the diagnostic MRI

  • Patients with contraindications for both treatment options

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Neurosurgery, Medical University of Vienna Vienna Austria 1090

Sponsors and Collaborators

  • Medical University of Vienna

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Josa M Frischer, MD, PhD, Principal Investigator, Medical University of Vienna
ClinicalTrials.gov Identifier:
NCT04857905
Other Study ID Numbers:
  • EK 1623/2020
First Posted:
Apr 23, 2021
Last Update Posted:
Apr 23, 2021
Last Verified:
Apr 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 Josa M Frischer, MD, PhD, Principal Investigator, Medical University of Vienna
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 23, 2021