Clinical Trial Finder

Inclusion Criteria:

• - Histological documentation of newly diagnosed malignant glioma.

• - ECOG performance status of 0 or 1.

• - Age ≥18.

• - Life expectancy of at least 12 weeks.

• - Hemoglobin ≥ 9.0 g/dl.

• - Granulocyte count ≥1.5 X 10^9/L.

• - Platelet count ≥100 X 10^9/L.

• - SGOT ≤ 2.5X upper limit of normal (ULN) - SGPT ≤ 2.5X upper limit of normal (ULN) - Alkaline phosphatase ≤4x ULN.

• - Serum creatinine ≤1.5X ULN.

• - Bilirubin ≤1.5X ULN.

• - Spontaneous PT-INR/PTT < 1.5x upper limit of normal (patients on therapeutic anticoagulation will be allowed to participate.

• - Patients must be on a stable or decreasing dose of corticosteroids for at least 2 weeks.

• - Patient for whom a first line treatment with temozolomide and radiotherapy is adequate.

• - Prophylactic anti-emetic, pentamidine inhalation / co-trimoxazole and anticonvulsants are allowed.

• - All patients must sign written informed consent.

Exclusion Criteria:

• - Prior treatment for high grade glioma.

• - Previous exposure to Ras pathway inhibitors.

• - Other concurrent active malignancy (with the exception of cervical carcinoma in situ or non melanoma carcinoma of the skin, superficial bladder tumor [Ta, Tis & T1] or any cancer curatively treated > 3 years prior to study entry).

• - Serious medical or psychiatric illness that would, in the opinion of the investigator, interfere with the prescribed treatment, including but not limited to: Congestive heart failure > NYHA class 2, active CAD, cardiac arrythmias requiring anti-arrythmic therapy or uncontrolled hypertension within the last 12 months.

• - Any condition limiting the patient's judgment capacity.

• - History of HIV infection, chronic hepatitis C or B as well as clinically active infections (> grade 2 NCI-CTC version 3.0) - History of organ allograft.

• - Renal dialysis.

• - Evidence or history of bleeding diathesis.

• - Major surgery within 4 weeks of start of study treatment, except for neurosurgical resection.

• - Autologous bone marrow transplant or stem cell rescue within 4 months of study.

• - Substance abuse, medical, psychological or social conditions that may interfere with the patient's participation in the study or evaluation of study results.

• - Medical condition that prevents the patient from swallowing pills.

• - Use of biologic response modifiers, such as G-CSF within 3 week of study entry.

• - Pregnant or breast-feeding women.

• - Refusal to use effective contraception.

Women of childbearing potential must have a negative pregnancy test performed within 7 days of the start of treatment. Both men and women enrolled in this trial must use adequate barrier birth control measures during the course of the trial and for at least 3 months after administration of study medication.

• - Known or suspected allergy to the investigational agent or any agent given in association with this trial.

Up to 18 patients will be included in this phase I study. The primary goal of this study will be to establish the maximum tolerated dose of sorafenib when used in combination with temozolomide and radiation therapy. Secondary goals of this study include: response rate, time to treatment failure, 6 month progression-free survival, event free survival and overall survival. A correlative study will investigate the pharmacokinetics of sorafenib used in combination with radiation therapy and temozolomide.

Arms

Experimental: Sorafenib dose titration

Interventions

Drug: - Sorafenib dose escalation

Sorafenib dose escalation scheme: 3 first patients: 200 mg/d, if dose limiting toxicities (DLT) not reached: 3 patients at 200 mg BID, if no DLT reached: 3 patients at 400 mg bid