Gliadel Wafer and Fluorescence-Guided Surgery With 5-ALA Followed by Radiation Therapy And Temozolomide in Treating Patients With Primary Glioblastoma
Glioblastoma
Bottom Line
View on ClinicalTrials.gov: NCT01310868 ↗Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- 5-ALA (Drug); Gliadel wafers (Drug); Radiotherapy as normal based on standard clinical protocols determined by the neuro-oncologist (Radiation); Concomitant chemotherapy as normal based on standard clinical protocols determined by the neuro-oncologist (Drug); Adjuvant chemotherapy as normal based on standard clinical protocols determined by the neuro-oncologist (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University College, London
- Primary completion
- Mar 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Safety, Tolerability, and Feasibility of Combination Intra-operative 5-ALA and Gliadel Wafers Prior to Adjuvant Radiotherapy Plus Temozolomide |
62; 9; 6; 45; 27; 2 | — |
| SECONDARY Time to Clinical Progression |
9.5 | — |
| SECONDARY Survival at 24 Months |
15 | — |
Summary
Eligibility Criteria
INCLUSION CRITERIA
i. The patient is reviewed at a specialist neuro-oncology multi-disciplinary team (MDT).
ii. Stealth MRI (neuronavigation) will be performed prior to surgery.
iii. Imaging is evaluated by a neuro-radiologist and judged to have typical appearances of a primary GBM
iv. Radical resection is judged to be realistic by the neurosurgeons at the MDT (i.e. NICE criteria for the use of Carmustine wafers can be met)
v. WHO performance status 0 or 1
vi. Age ≥18
vii. Patient judged by MDT to be fit for standard radical aggressive therapy for GBM (resection followed by RT with concomitant and adjuvant temozolomide)
EXCLUSION CRITERIA
i. GBM thought to be transformed low grade or secondary disease
ii. The patient has not been seen by a specialist MDT.
iii. There is uncertainty about the radiological diagnosis
iv. 5-ALA or Carmustine wafers is contra-indicated (inc known or suspected allergies to 5-ALA or porphyrins, or acute or chronic types of porphyria)
v. Pregnant or lactating women
vi. Known or suspected HIV or other significant infection or comorbidity that would preclude radical aggressive therapy for GBM
vii. Active liver disease (ALT or AST ≥5 x ULRR)
viii. Concomitant anti-cancer therapy except steroids
ix. History of other malignancies (except for adequately treated basal or squamous cell carcinoma or carcinoma in situ) within 5 years
x. Previous brain surgery (including biopsy) or cranial radiotherapy
xi. Platelets <100 x109/L
xii. Mini mental status score <15
Data sourced from ClinicalTrials.gov (NCT01310868). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.