Phase II Open Label, Non-randomized Study of Sorafenib and Everolimus in Relapsed and Non-resectable Osteosarcoma

Exclusion Criteria

• •Dementia or significantly altered mental status that would prohibit the understanding or rendering of informed consent and compliance with the requirements of this protocol
• •Patients with any severe and/or uncontrolled medical conditions such as unstable angina pectoris, symptomatic congestive heart failure, myocardial infarction ≤6months, serious uncontrolled cardiac arrhythmia, uncontrolled hyperlipidemia, active or uncontrolled severe infection, cirrhosis, chronic or persistent active hepatitis or severely impaired lung function.
• •History of HIV infection and active clinically serious infections (\>grade 2 according to NCI-CTCAE vs. 4.0)
• •Symptomatic metastatic brain or meningeal tumors (unless the patient is \>6months from definitive therapy, has a negative imaging study within 4weeks of study entry and is clinically stable with respect to the tumor at the time of study entry)
• •Patients with seizure disorders requiring medication
• •Pregnant or breast-feeding patients. Women of childbearing potential must have a negative pregnancy test performed within 7days of the start of treatment. Both men and women must use adequate barrier birth control measures during the course of the trial and 8weeks after last dose of study drug
• •Patients with evidence or history of bleeding diathesis
• •Patients undergoing renal dialysis
• •Patients unable to swallow oral medications
• •Uncontrolled diabetes (fasting glucose\>2xULN)
• •Patients receiving chronic, systemic treatment with corticosteroids or another immunosuppressive agent (except corticosteroids with a daily dosage equivalent to prednisone ≤20mg for adrenal insufficiency). Patients receiving corticosteroids must be on a stable dose for ≥4weeks prior to the first dose of Everolimus. Topical or inhaled corticosteroids are permitted
• •Patients with a history of another malignancy within 5years prior to study entry, except curatively treated non-melanotic skin cancer or in-situ cervical cancer skin or other solid tumors curatively treated with no evidence of disease for ≥3years. Patients with severe and/or uncontrolled concurrent medical disease that in the opinion of the investigator could cause unacceptable safety risks or compromise compliance with the protocol
• •Anticancer chemotherapy or immunotherapy during the study or within 4weeks of study entry
• •Radiotherapy during study or within 3weeks of start of study drug. (Palliative radiotherapy will be allowed)
• •Major surgery within 4weeks of start of study
• •Investigational drug therapy outside of this trial during or within 4weeks of study entry
• •Prior exposure to the study drugs or their analogues
• •Patients with known hypersensitivity to sorafenib, everolimus or other rapamycin analogs, or to its excipients
• •Substance abuse, medical, psychological or social conditions that may interfere with the patient's participation in the study or evaluation of the study results
• •A history of noncompliance to medical regimens or inability or unwillingness to return for scheduled visits