A Phase II Study Of Gliadel, Concomitant Temozolomide And Radiation, Followed By Dose Dense Therapy With Temozolomide Plus Bevacizumab For Newly Diagnosed Malignant High Grade Glioma

Glioma Clinical Trial

— KARE004  

Official title:

A Phase II Study Of Gliadel, Concomitant Temozolomide And Radiation, Followed By Dose Dense Therapy With Temozolomide Plus Bevacizumab For Newly Diagnosed Malignant High Grade Glioma

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT00660621
• Other study ID #: KARE004
• Secondary ID: KARE004
• Status: Recruiting
• Phase: Phase 2
• First received: April 14, 2008
• Last updated: January 18, 2010
• Start date: April 2008
• Est. completion date: December 2010

Study information

• Verified date: January 2010
• Source: Kentuckiana Cancer Institute
• Contact: Leslie Haysley
• Phone: 502-561-8200
• Email: lhaysley[@]kci.us
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

To determine the safety and efficacy of surgical resection with Gliadel® 3.85% wafer implantation, followed by concomitant limited field radiation therapy and temozolomide, followed by dose dense temozolomide and bevacizumab in subjects undergoing initial surgery for newly-diagnosed high grade glioma.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 40
• Est. completion date: December 2010
• Est. primary completion date: December 2010
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Subjects, men and women, must be between ages 18 and 75 years.

• Subjects must have radiographic evidence on cranial magnetic resonance imaging (MRI) of a single, contrast-enhancing unilateral supratentorial cerebral tumor.

• Surgery is recommended within 4 weeks of the baseline MRI scan.

• Subjects must have a Karnofsky Performance Score of 60 or higher.

• Subjects must have signed an Institutional Review Board (IRB)-approved informed consent prior to any non-standard of care study procedure or no later than the start of dose dense temozolomide and bevacizumab..

• Subjects must have a pathological diagnosis of a high grade (IV) malignant glioma.

• Subjects, both men and women, must be willing to avoid pregnancy for up to 2 years after wafer implantation surgery and be counseled regarding the unknown, and potentially harmful, risks to the embryo or fetus from participation in this study.

Exclusion Criteria:

• Subjects who have had prior cytoreductive surgery for high-grade glioma. Subjects who have had a diagnostic stereotactic biopsy are eligible.

• Subjects with more than one focus of tumor or tumor crossing the midline as assessed by coronal cranial MRI scan.

• Concomitant significant life-threatening disease from which the subject could reasonably be expected to die within the first 12 months of the study.

• Known hypersensitivity reactions to temozolomide, nitrosoureas or any other components of the Gliadel® wafer.

• Prior CNS radiotherapy.

• Subjects who have received any prior chemotherapy for this malignant glioma prior to the baseline evaluation or subjects who are currently being treated with chemotherapeutic agents.

• Subjects with fewer than 100,000 platelets per mm3 or fewer than 3.500 leukocytes per mm3.

• Liver function tests greater than or equal to 2.5 times the upper limit of normal (transaminases (SGOT, SGPT), total bilirubin, alkaline phosphatase).

• Serum creatinine equal to or greater than 1.5 times the upper limit of normal, blood urea nitrogen (BUN) equal to or greater than 2.5 times the upper limit of normal.

• Pregnancy, or lactating females or females of childbearing potential not using adequate contraception.

• Participation in any other investigational protocol in the prior twelve months for any type of malignancy.

• Psychological, familial, sociological or geographical conditions which do not permit adequate medical follow-up and compliance with the study protocol.

• Inadequately controlled hypertension (blood pressure systolic > 150 mmHg or diastolic > 100 mmHg).

• Unstable angina or history of myocardial infarction within six months prior to enrollment.

• Evidence of bleeding, diathesis, or coagulopathy. Chronic full-dose anticoagulation with warfarin is not permitted though subjects may be on low molecular weight heparin or fondaparinux.

• Serious non-healing wound, ulcer, or bone fracture.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Glioma

Intervention

Drug:
• Temozolomide and Bevacizumab
Between 14 and 28 days after surgery, all subjects will begin a standard course of post-operative limited field radiation therapy to the tumor site and a surrounding margin with concomitant temozolomide at a daily dose of 75 mg/m2 (7 days/week). No later than 45 days after date of completion of radiation therapy, all subjects will begin dose dense temozolomide at dose of 150 mg/m2 on Days 1-7 and 15-21 of a 28 day cycle with concomitant bevacizumab 10mg/kg administered intravenously every other week.

Locations

Country	Name	City	State
United States	Kentuckiana Cancer Institute	Louisville	Kentucky

Sponsors (2)

Lead Sponsor	Collaborator
Kentuckiana Cancer Institute	Eisai Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety and efficacy of concomitant limited field radiation therapy and temozolomide, followed by dose dense temozolomide and bevacizumab in subjects undergoing initial surgery for newly-diagnosed high grade glioma.		First 5 subjects after 6 months.	Yes