Intraoperative Radiotherapy in Newly Diagnosed Glioblastoma Multiforme
Sponsor: Universitätsmedizin Mannheim
ClinicalTrials ID:NCT02685605
INTRAGO II is a phase III trial evaluating if intraoperative radiotherapy (IORT) enhances median progression-free survival in newly diagnosed glioblastoma multiforme patients. Participants undergo standard surgery, IORT (20-30 Gy), and radiochemotherapy (60 Gy EBRT with temozolomide). Eligibility includes newly diagnosed GBM patients suitable for surgery and radiochemotherapy.
Patient Parameters
| Parameter | Options |
|---|
Program Overview
INTRAGO II resembles a multicentric, prospective, randomized, 2-arm, open-label clinical phase III trial which tests if the median progression-free survival (PFS) of patients with newly diagnosed glioblastoma multiforme (GBM) can be improved by the addition of intraoperative radiotherapy (IORT) to standard radiochemotherapy.
Eligibility Criteria
Inclusion Criteria
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Age ≥18 and ≤ 80 years
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Karnofsky Performance Score (KPS) ≥ 60%
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Supratentorial T1-Gd enhancing lesion(s) amenable to total resection
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Legal capacity and ability of subject to understand character and individual consequences of the clinical trial
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Patient's written IC obtained at least 24h prior to surgery
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For women with childbearing potential: adequate contraception
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Patients must have adequate organ functions
Bone marrow function:
- Platelets ≥ 75.000/μL
- WBC ≥ 3.000/μL
- Hemoglobin ≥ 10.0 g/dL
Liver Function:
- ASAT and ALAT ≤ 3.0 times ULN
- ALP ≤ 2.5 times ULN
- Total Serum Bilirubin < 1.5 times ULN
Renal Function:
- Serum Creatinine ≤ 1.5 times ULN
Inclusion Criteria Related to Surgery:
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IORT must be technically feasible
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Histology supports diagnosis of GBM
Exclusion Criteria
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Multicentric disease (e.g. in both hemispheres) or non-resectable satellite lesions
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Previous cranial radiation therapy
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Cytostatic therapy / chemotherapy for cancer within the past 5 years
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History of cancers or other comorbidities that limit life expectancy to less than five years
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Previous therapy with anti-angiogenic substances (such as bevacizumab)
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Technical impossibility to use MRI or known allergies against MRI and/or CT contrast agents
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Participation in other clinical trials testing cancer-derived investigational agents/procedures.
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Pregnant or breast feeding patients
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Fertile patients refusing to use safe contraceptive methods during the study
Exclusion Criteria Related to Surgery:
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Active egress of fluids from a ventricular defect
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In-field risk organs and/or IORT dose >8 Gy to any risk organ
Locations
| FACILITY | ZIP | CITY | STATE |
|---|---|---|---|
| Barrow Neurological Institute (SJHMC) | 85013 | Phoenix | Arizona |
| Stritch School of Medicine Loyola University | 60153 | Maywood | Illinois |
| Long Island Jewish Medical Center, North Shore University Hospital | 11042 | Lake Success | New York |
| Lenox Hill Hospital, Hofstra Northwell School of Medicine | 10028 | New York | New York |
| West Virginia University | 26506-9260 | Morgantown | West Virginia |
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