Phase II Trial for Patients With Glioblastoma Multiforme (GBM) Treated With Gliadel Followed by Avastin Plus Irinotecan
Overview
- Phase
- Phase 2
- Intervention
- Gliadel/Avastin/CPT-11
- Conditions
- Malignant Glioma
- Sponsor
- Duke University
- Enrollment
- 18
- Locations
- 1
- Primary Endpoint
- 24-week Overall Survival
- Status
- Terminated
- Last Updated
- 13 years ago
Overview
Brief Summary
The primary objective of the study is to use 24 week survival to assess the efficacy of the combination of Gliadel followed by Avastin and irinotecan in the treatment of grade IV malignant glioma patients following surgical resection. The secondary objectives are to determine the progression-free survival following the combination of Gliadel followed by Avastin and irinotecan and to describe the toxicity of Gliadel followed by Avastin and irinotecan.
Detailed Description
This is a phase II study of the combination of Gliadel followed by Avastin and irinotecan in grade IV malignant glioma patients. The study will have survival and toxicity endpoints. Subjects will be identified by the investigator as those patients who have histologically documented grade IV malignant glioma (glioblastoma multiforme or gliosarcoma) with recurrent or progressive disease who are able to undergo a gross total resection (GTR). Part I: Gliadel wafer- 1-8 wafers inserted at time of gross total resection. Treatment cycle is 42 days in length. For patients with ≥ Grade 1 toxicity will allow 84 days prior to beginning therapy with Avastin and Irinotecan (CPT-11). Part II: Avastin Plus Irinotecan (Cycles 1-12) consists of the following (cycle length is 6 weeks): * Irinotecan 125 mg/m2 (not taking enzyme-inducing anti-epileptic drugs (EIAEDs)) or 340 mg/m2 (taking EIAEDs) given every two weeks on days 1, 15, 29, etc.; * If the patient has the uridine diphosphate (UDP) glucuronosyltransferase 1 family, polypeptide A1 (UGT1A1) polymorphism (7/7), they do not metabolize the irinotecan normally, so these patients will start out at a two dose level reduction; For patients on an EIAED, the starting dose will be 275 mg/M2, and for patients not on an EIAED, the starting dose will be 75 mg/M2; * Avastin 10 mg/kg immediately after the irinotecan given every 2 weeks on days 1, 15, 29, etc. The primary objective of this phase II study is to determine whether the administration of Gliadel wafers followed by Avastin and irinotecan to patients with recurrent GBM is a treatment regimen worthy of further investigation in a randomized clinical trial. The basis for making this decision will be the proportion of patients who survive at least 24 weeks after initiation of protocol treatment. In the initial Phase I and II clinical trials, four potential Avastin-associated safety signals were identified: hypertension, proteinuria, thromboembolic events, and hemorrhage. The two major toxicities associated with irinotecan are myelosuppression and diarrhea. Side effects associated with Gliadel are seizures, brain edema (swelling), healing abnormalities, wound infection and body pain.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients must have histologically confirmed diagnosis of WHO grade IV primary malignant glioma (glioblastoma multiforme or gliosarcoma). Patients have to be able to undergo a GTR.
- •Age \> or = 18 years
- •Evidence of a unilateral, single focus of measurable central nervous system (CNS) neoplasm on contrast-enhanced MRI, unless medically contraindicated (CT scan will then be used)
- •Patients must have \< or = 2 disease progressions
- •An interval of at least 4 weeks from the end of prior radiotherapy or one week from the end of a cycle of chemotherapy and enrollment on this protocol
- •Karnofsky \> or = 70%
- •Hemoglobin \> or = 9.0 g/dl, absolute neutrophil count (ANC) \> or = 1,500 cells/microliters, platelets \> or = 125,000 cells/microliters
- •Serum creatinine \< or = 1.5 mg/dl, serum glutamic-oxaloacetic transaminase (SGOT) and bilirubin \< or = 1.5 times upper limit of normal
- •Patients on corticosteroids must have been on a stable dose for 1 week prior to entry, if clinically possible, and the dose should not be escalated over entry dose level
- •If patient received chemotherapy or investigational agent as part of their prior therapy, the patient must recover from all toxicities (\> or = Grade 1) prior to enrollment on this protocol
Exclusion Criteria
- •Pregnancy or breast feeding. Women of childbearing potential must have a negative serum pregnancy test within 72 hours prior to treatment administration
- •Multifocal disease
- •Prior treatment with Gliadel
- •Prior treatment with CPT-11 or Avastin
- •Prior stereotactic radiosurgery or brachytherapy
- •Co-medication that may interfere with study results; e.g. immuno-suppressive agents other than corticosteroids
- •Active infection requiring IV antibiotics
- •Acute or chronic renal insufficiency (a glomerular filtration rate (GFR) \<30 mL/min/1.73m2) or acute renal insufficiency of any severity due to hepato-renal syndrome or in the peri-operative liver transplantation period
- •Inability, in the opinion of the study investigator, to comply with study and/or follow-up procedures
- •Current, recent (within 4 weeks of the first infusion of this study), or planned participation in an experimental drug study other than a Genentech-sponsored Avastin cancer study
Arms & Interventions
Gliadel/Avastin/CPT-11
Gliadel/Avastin/CPT-11
Intervention: Gliadel/Avastin/CPT-11
Outcomes
Primary Outcomes
24-week Overall Survival
Time Frame: 24 weeks
The percentage of participants surviving 24 weeks from the start of study treatment
Secondary Outcomes
- 24-week Progression-free Survival (PFS)(24 weeks)
- Median Progression-free Survival (PFS)(Time in months from the start of study treatment to the date of first progression according to modified Macdonald criteria or to death due to any cause, assessed up to 47 months)
- Median Overall Survival (OS)(Time in months from the start of study treatment to date of death due to any cause, assessed up to 47 months)
- Incidence and Severity of Central Nervous System (CNS) Hemorrhage(47 months)
- Incidence of Grade ≥ 4 Hematologic and ≥ Grade 3 Non-hematologic Toxicities(47 months)