Overview

Combining Sunitinib, Temozolomide and Radiation to Treat Patients Diagnosed With Glioblastoma

Status:
Unknown status
Trial end date:
2017-06-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to determine whether a combination of Sunitinib, Temozolomide and Radiation Therapy would be effective in the treatment of newly diagnosed Glioblastoma patients harboring tumors with unmethylated MGMT promoter.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Bassam Abdulkarim
Collaborators:
Canadian Cancer Society (CCS)
Canadian Cancer Society Research Institute (CCSRI)
Pfizer
Treatments:
Dacarbazine
Sunitinib
Temozolomide
Criteria
Inclusion Criteria:

- Histologically documented newly diagnosed GBM patients

- Unmethylated MGMT promoter as determined by Methylation specific-polymerase chain
reaction (MGMT(+) tumor)

- Age between 18 to 70

- Karnofsky performance status ≥70

- History and physical examination including neurologic examination within 4 weeks prior
to registration

- Systolic blood pressure ≤ 160 mmHg or diastolic pressure ≤ 100mm Hg

- Required blood work within 14 days prior to registration

- Eligible for standard concurrent chemoradiation with TMZ

- Patients must have normal organ and marrow functions as defined below:

- Absolute neutrophil count ≥ 1.5x 109/L

- Platelets ≥100x 109/L

- Hemoglobin ≥80g/L

- International Normalized Ratio ≤1.3

- Creatinine ≤1.5x [upper limit of normal] Or creatinine clearance ≥60
mL/min/1.73m2

- Normal baseline thyroid function as measured by a thyrotropic-stimulating hormone
within institutional normal limits

- Adequate liver function: Alanine transaminase or Aspartate transaminase < 2 x upper
limit of normal and bilirubin 1.6 mg/dL. No active bleeding or pathologic condition
that carries high risk of bleeding (e.g. tumor involving major vessels or known
varices)

- Patients who have undergone resection must meet the following conditions:

- Patients must have recovered from the effects of surgery and a minimum of 14 to
28 days must have elapsed from the day of surgery to day of registration. Day of
registration is considered the first day of Sunitinib.

- For stereotactic biopsy, a minimum of 14 days must have elapsed prior to
registration

- No prior RT to the brain, chemotherapy, or anti-angiogenic therapy

- Estimated life expectancy of at least 6 months

- Premenopausal women must have a negative human chorionic gonadotropin within 14 days
prior to registration

- The effects of Sunitinib on the developing human fetus is unknown. Women of
childbearing potential and male participants must practice adequate contraception.
Should a woman become pregnant or suspect she is pregnant during the study, she should
inform her treating physician immediately.

- Ability to understand and the willingness to sign a written informed consent document

Exclusion Criteria:

- Histologically documented newly diagnosed GBM patients with methylated MGMT promoter

- Serious medical conditions that might be aggravated by treatment, including but not
limited to: myocardial infarction within 6 months, congestive heart failure, unstable
angina, active cardiomyopathy, unstable ventricular arrhythmia, uncontrolled
hypertension, uncontrolled psychotic disorders, serious infections, active peptic
ulcer disease, active liver disease or cerebrovascular disease with previous stroke

- Patients with a history of coagulopathy

- Evidence of intratumoural or peritumoural hemorrhage deemed significant by the
treating physician

- ≥ 1+ proteinuria on two successive urine dipstick assessments

- thrombolytic therapy within 4 weeks

- Patient with prolonged of corrected QT interval of more than 450 msec in screening EKG
will be excluded

- Women who are pregnant or nursing

- History of allergic reactions attributed to compounds of similar chemical or biologic
composition to Sunitinib

- Previous treatment with Sunitinib or other inhibitors of the vascular endothelial
growth factor signalling axis

- Bleeding disorders

- Concurrent use of anticoagulant or antiplatelet drugs

- Patients with any condition that impairs their ability to swallow Sunitinib (e.g.
gastrointestinal tract disease resulting in an inability to take oral medication or a
requirement for IV alimentation, prior surgical procedures affecting absorption, or
active peptic ulcer disease).

- HIV-positive patients on combination antiretroviral therapy are ineligible because of
the potential for pharmacokinetic interactions with Sunitinib. In addition, these
patients are at increased risk of lethal infections when treated with bone
marrow-suppressive therapy

- Individuals with MRI non-compatible metal in the body, or unable to undergo MRI
procedures.

- Allergy to gadolinium

- Patients with severe liver impairment will not be enrolled in this study.