Generic Name |
Temozolomide | |
---|---|---|
IND |
||
Brand Name (US) |
Temodar | |
Manufacturer |
Schering-Plough | |
Drug Type |
Chemotherapy | |
Delivery |
Oral | |
Approval Status |
Approved for a non-GIST cancer | |
Indications |
Giioblastoma Multiforme, Refractory Anaplastic Astrocytoma | |
Overall Strategy |
GIST cell based | |
Strategy |
Interfere with DNA replication | |
Drug Category |
SDH-directed |
In a phase II trial for sarcoma (that included 19 GIST patients), the median time to disease progression was 2.3 months in patients with GISTs and 3.3 months in patients with other STSs. The authors conclusions were: The data from the current study suggest that temozolomide is well tolerated but has only minimal efficacy and a limited role in the treatment of patients with STSs.
Temozolomide is an imidazotetrazine derivative of the alkylating agent dacarbazine. It undergoes rapid chemical conversion in the systemic circulation at physiological pH to the active compound, MTIC (monomethyl triazeno imidazole carboxamide). Temozolomide exhibits schedule-dependent antineoplastic activity by interfering with DNA replication. Temozolomide has demonstrated activity against recurrent glioma. In a recent randomized trial, concomitant and adjuvant temozolomide chemotherapy with radiation significantly improves progression free survival and overall survival in glioblastoma multiforme patients.