Clinical data | |
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Trade names | Vumon |
AHFS/Drugs.com | Monograph |
MedlinePlus | a692045 |
Pregnancy category |
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Routes of administration |
Intravenous |
ATC code | |
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Legal status |
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Pharmacokinetic data | |
Bioavailability | N/A |
Protein binding | >99% |
Metabolism | Hepatic (CYP2C19-mediated) |
Biological half-life | 5 hours |
Excretion | Renal and fecal |
Identifiers | |
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Synonyms | VM-26 |
CAS Number | |
PubChem CID | |
IUPHAR/BPS | |
DrugBank | |
ChemSpider | |
UNII | |
KEGG | |
ChEBI | |
ChEMBL | |
ECHA InfoCard | 100.045.286 |
Chemical and physical data | |
Formula | C32H32O13S |
Molar mass | 656.655 g/mol |
3D model (Jmol) | |
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(what is this?) |
Teniposide (trade name Vumon) is a chemotherapeutic medication used in the treatment of childhood acute lymphocytic leukemia (ALL), Hodgkin's lymphoma, certain brain tumours, and other types of cancer. It is in a class of drugs known as podophyllotoxin derivatives and slows the growth of cancer cells in the body.
Teniposide is used for the treatment of a number of cancer types in children. In the US, it is approved for the second-line therapy of acute lymphocytic leukemia (ALL) in combination with other antineoplastic drugs. In Europe, it is also approved for the treatment of Hodgkin's lymphoma, generalized malignant lymphoma, reticulocyte sarcoma, acute leukaemia, primary brain tumours (glioblastoma, ependymoma, astrocytoma), bladder cancer, neuroblastoma and other solid tumours in children.
The medication is injected though a vein and burns if it leaks under the skin. It can be used in combination with other anticancer drugs.
The drug is contraindicated during pregnancy and lactation, in patients with severe liver or kidney impairment or severely impaired haematopoiesis.
Teniposide, when used with other chemotherapeutic agents for the treatment of ALL, results in severe bone marrow suppression. Other common side effects include gastrointestinal toxicity, hypersensitivity reactions, and reversible alopecia.