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

NCT ID: NCT03055208

Last Updated: 2023-05-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

SUSPENDED

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-02-08

Study Completion Date

2023-05-09

Brief Summary

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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

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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.

Conditions

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Glioblastoma

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Radiosurgery

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).

Group Type EXPERIMENTAL

gamma knife radiosurgery (15 Gy to 50% isodose)

Intervention Type RADIATION

Radiosurgery with a gamma knife resembles the application of a precisely focused, high single dose of ionizing irradiation.

Interventions

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gamma knife radiosurgery (15 Gy to 50% isodose)

Radiosurgery with a gamma knife resembles the application of a precisely focused, high single dose of ionizing irradiation.

Intervention Type RADIATION

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Universitätsmedizin Mannheim

OTHER

Sponsor Role lead

Responsible Party

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Frank A. Giordano

Interim Head, Department of Radiation Oncology

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Frank A Giordano, MD

Role: PRINCIPAL_INVESTIGATOR

University Medical Center Mannheim

Locations

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Department of Radiotherapy University Hospital Mannheim

Mannheim, , Germany

Site Status

Countries

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Germany

Other Identifiers

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Gamma-GBM

Identifier Type: -

Identifier Source: org_study_id

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