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Early Stereotactic Gamma Knife Radiosurgery to Residual Tumor After Surgery of Newly Diagnosed Glioblastoma (Gamma-GBM)

Primary Purpose

Glioblastoma

Status
Suspended
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
gamma knife radiosurgery (15 Gy to 50% isodose)
Sponsored by
Universitätsmedizin Mannheim
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Glioblastoma focused on measuring Glioblastoma, Radiosurgery, Gamma Knife

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 18
  • Karnofsky performance status score ≥ 60
  • histology must be glioblastoma (frozen sections during surgery)
  • radiographic proof of residual tumor
  • Informed consent
  • adequate birth control (e.g., oral contraceptives)

Exclusion Criteria:

  • any previous cranial radiotherapy
  • histology inconclusive or low(er)-grade astrocytoma
  • contraindications for chemo- or radiotherapy
  • bleeding or clotting disorders
  • contraindications for MRI or CT scans

Sites / Locations

  • Department of Radiotherapy University Hospital Mannheim

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Radiosurgery

Arm Description

Following intraoperative confirmation of glioblastoma (frozen section): Early (24-72h post surgery) stereotactic ablation (gamma knife radiosurgery) of residual tumor (defined in early postoperative T1-weighted MRI scanning with and without contrast), followed by standard-of-care therapy (chemo-radiotherapy with 60 Gy external beam radiation therapy (EBRT) and 75 mg/m2/d temozolomide, followed by adjuvant chemotherapy with 150-200 mg/m2/d/cycle temozolomide in a 5/28 days schedule).

Outcomes

Primary Outcome Measures

Median Progression-Free Survival Time (PFS)
PFS is defined as the time span of initial diagnosis (i.e., the day of surgery) until tumor progression is confirmed in follow-up MRI scans. All scans will be assessed using modified Response Assessment in Neuro-Oncology (RANO) criteria or until death by any cause.

Secondary Outcome Measures

Median Overall Survival Time (OS)
OS is defined as the time span of initial diagnosis (i.e., the day of surgery) until death by any cause.
Radiation-related (acute / early delayed / late) neurotoxicity
Assessed by regular neurological examinations
Incidence of symptomatic radionecrosis
Assessed by serial MRI scans

Full Information

First Posted
February 9, 2017
Last Updated
May 9, 2023
Sponsor
Universitätsmedizin Mannheim
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1. Study Identification

Unique Protocol Identification Number
NCT03055208
Brief Title
Early Stereotactic Gamma Knife Radiosurgery to Residual Tumor After Surgery of Newly Diagnosed Glioblastoma
Acronym
Gamma-GBM
Official Title
Early Stereotactic Gamma Knife Radiosurgery to Residual Tumor After Surgery of Newly Diagnosed Glioblastoma
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Suspended
Why Stopped
suspended due to low accrual rates
Study Start Date
February 8, 2017 (Actual)
Primary Completion Date
March 30, 2020 (Actual)
Study Completion Date
May 9, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universitätsmedizin Mannheim

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Gamma GBM is a single-arm phase II trial that prospectively measures the progression-free survival time after addition of an early gamma knife boost to areas of residual tumor to standard-of-care (surgery, chemo-radiotherapy, chemotherapy).
Detailed Description
Glioblastomas are highly malignant brain tumors that recur about 6 months after treatment. Most recurrences develop at the edge of the surgical margin and a common reason for an early recurrence of a glioblastoma is when tumors are not completely resected. This may be the case when intraoperative neuro-monitoring indicates that further resection would impair certain motor functions. Physicians can identify residual tumor in early (24-72h after surgery) postoperative MRI scans and could treat these regions. However, this treatment would not be a part of the recommended standard of care and thus, any further treatment of this areas will need a clinical trial. The aim of this trial is to evaluate if the use of another modality to deplete these areas of residual tumor identified in early postoperative MRI scans will provide a relevant benefit in terms of progression-free survival (which means a prolongation of the time that patients do not experience a re-growth of the tumor). The modality is termed "radiosurgery", which is a non-invasive technique to delete cells without using a blade but a highly focused beam of gamma rays. The machine that focusses these rays (like a magnifying glass that can focus light), is called 'gamma knife'. Gamma knife radiosurgery is a safe and effective treatment for a plethora of malignant and benign brain tumors and the technique is used since the 1950s and there has been a continuous improvement of precision and patient comfort up to now.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glioblastoma
Keywords
Glioblastoma, Radiosurgery, Gamma Knife

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Radiosurgery
Arm Type
Experimental
Arm Description
Following intraoperative confirmation of glioblastoma (frozen section): Early (24-72h post surgery) stereotactic ablation (gamma knife radiosurgery) of residual tumor (defined in early postoperative T1-weighted MRI scanning with and without contrast), followed by standard-of-care therapy (chemo-radiotherapy with 60 Gy external beam radiation therapy (EBRT) and 75 mg/m2/d temozolomide, followed by adjuvant chemotherapy with 150-200 mg/m2/d/cycle temozolomide in a 5/28 days schedule).
Intervention Type
Radiation
Intervention Name(s)
gamma knife radiosurgery (15 Gy to 50% isodose)
Intervention Description
Radiosurgery with a gamma knife resembles the application of a precisely focused, high single dose of ionizing irradiation.
Primary Outcome Measure Information:
Title
Median Progression-Free Survival Time (PFS)
Description
PFS is defined as the time span of initial diagnosis (i.e., the day of surgery) until tumor progression is confirmed in follow-up MRI scans. All scans will be assessed using modified Response Assessment in Neuro-Oncology (RANO) criteria or until death by any cause.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Median Overall Survival Time (OS)
Description
OS is defined as the time span of initial diagnosis (i.e., the day of surgery) until death by any cause.
Time Frame
2 years
Title
Radiation-related (acute / early delayed / late) neurotoxicity
Description
Assessed by regular neurological examinations
Time Frame
2 years
Title
Incidence of symptomatic radionecrosis
Description
Assessed by serial MRI scans
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 Karnofsky performance status score ≥ 60 histology must be glioblastoma (frozen sections during surgery) radiographic proof of residual tumor Informed consent adequate birth control (e.g., oral contraceptives) Exclusion Criteria: any previous cranial radiotherapy histology inconclusive or low(er)-grade astrocytoma contraindications for chemo- or radiotherapy bleeding or clotting disorders contraindications for MRI or CT scans
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frank A Giordano, MD
Organizational Affiliation
University Medical Center Mannheim
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Radiotherapy University Hospital Mannheim
City
Mannheim
ZIP/Postal Code
68167
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Early Stereotactic Gamma Knife Radiosurgery to Residual Tumor After Surgery of Newly Diagnosed Glioblastoma

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