Intraoperative Radiotherapy in Newly Diagnosed Glioblastoma Multiforme

Sponsor: Universitätsmedizin Mannheim

Sponsor score: 0

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

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

  1. Age ≥18 and ≤ 80 years

  2. Karnofsky Performance Score (KPS) ≥ 60%

  3. Supratentorial T1-Gd enhancing lesion(s) amenable to total resection

  4. Legal capacity and ability of subject to understand character and individual consequences of the clinical trial

  5. Patient's written IC obtained at least 24h prior to surgery

  6. For women with childbearing potential: adequate contraception

  7. 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:

  8. IORT must be technically feasible

  9. Histology supports diagnosis of GBM

Exclusion Criteria

  1. Multicentric disease (e.g. in both hemispheres) or non-resectable satellite lesions

  2. Previous cranial radiation therapy

  3. Cytostatic therapy / chemotherapy for cancer within the past 5 years

  4. History of cancers or other comorbidities that limit life expectancy to less than five years

  5. Previous therapy with anti-angiogenic substances (such as bevacizumab)

  6. Technical impossibility to use MRI or known allergies against MRI and/or CT contrast agents

  7. Participation in other clinical trials testing cancer-derived investigational agents/procedures.

  8. Pregnant or breast feeding patients

  9. Fertile patients refusing to use safe contraceptive methods during the study

    Exclusion Criteria Related to Surgery:

  10. Active egress of fluids from a ventricular defect

  11. In-field risk organs and/or IORT dose >8 Gy to any risk organ

Locations

FACILITYZIPCITYSTATE
Barrow Neurological Institute (SJHMC)85013PhoenixArizona
Stritch School of Medicine Loyola University60153MaywoodIllinois
Long Island Jewish Medical Center, North Shore University Hospital11042Lake SuccessNew York
Lenox Hill Hospital, Hofstra Northwell School of Medicine10028New YorkNew York
West Virginia University26506-9260MorgantownWest Virginia

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