Inclusion Criteria:

- Osteosarcoma histological confirmation.

- No option of known curative treatment, neither approved treatment that increases
survival with adequate quality of life.

- Karnofsky scale ≥ 50 for patients over 16 years and Lansky scale ≥ 50 for patients
under 16 years.

- Subjects should not have received antineoplastic therapy < 4 weeks before study
treatment initiation.

- Adequate hematological function: neutrophil count > 1.500/mm³, platelets >
100.000/mm³ and hemoglobin > 8.0 mg/dL.

- Adequate renal function, as defined below:

Age Maximum serum creatinine (mg/dL) 0 - 29 days 0,4 - 0,7 1
month - 3 years 0,7 4 - 7 years 0,8 8 - 10 years 0,9 11 - 12 years
1,0 13 - 17 years 1,2

≥18 years 1,3

- Adequate hepatic function: total bilirubin ≤ 1.5 x ULN and transaminases ≤ 2.5 x ULN.

- Patient and/or legal responsible must sign ICF.

- Life expectation > 8 weeks.

- Measurable disease, according to RECIST criteria.

- For female patients of childbearing age: Presence of a negative pregnancy test within
7 days prior to day 0.

- The patient agrees to use effective contraception if procreative potential exists.
Use of reliable means of contraception (e.g. hormonal contraceptive, patch, vaginal
ring, intrauterine device, physical barrier, abstinence) for subjects of reproductive
potential (males and females) is required during study treatment and for 3 months
following last dose of study drug

Exclusion Criteria:

- History of myocardial infarction, angina or cerebrovascular accident related to
atherosclerosis.

- Pulmonary disorder (e.g. FEV1 or DLCO ≤ 70% upper expected).

- Significant hematologic or hepatic abnormality (transaminases levels > 2.5 x ULN or
serum bilirubin >1.5 x ULN, hemoglobin < 8 g/dL, platelets < 100.000/ mm3, ANC <
1.500/mm3).

- Has other existing serious medical conditions that could adversely affect the ability
of the patient to be treated in accordance with the protocol.

- Any condition, therapy, or medical condition, which, in the opinion of the attending
physician could represent a risk for the patient or adversely affect the study
objectives.

- If female, is pregnant or lactating.

- Active infection at the moment of recruitment.

- Previous history of organ transplantation.

- Recent surgery < 2 months before entering study.

- Concomitant antineoplastic therapy.

- Patient received more than one rescue treatment, previously.

- Previous treatment with mTor inhibitors (ex: sirolimus, temsirolimus, everolimus).

- Use of investigational drug < 30 days before entering study.

- Non-controlled hyperlipidaemia: serum cholesterol (fasting) > 300 mg/dL or 7,75
mmol/L and triglycerides (fasting) > 2,5 x ULN.

- Non-controlled diabetes mellitus defined as: glycemia (fasting) > 1.5 x ULN.

- Patient with hemorrhagic disorder or using oral anti-vitamin K (except warfarin in
low doses).

- Patient with HIV infection.

- Incapable to perform protocol visits.

- Another neoplasia for the last 2 years (except squamous or basocellular skin cancer).

- Hypersensitivity history to rapamycin analogs.

- Chronic treatment with corticoids (except per oral, topical or local treatment) or
another immunosuppressor agent.