EPIPODOPHYLLOTOXINS
Etoposide is a semisynthetic derivative of podophyllotoxin, whichis
extracted from the mayapple root (Podophyllum
peltatum). Intravenous and oral formulations of etoposide are approved for
clinical use in the USA. The oral bioavailability is about 50%, requiring the
oral dose to be twice that of an intravenous dose. Up to 30–50% of drug is
excreted in the urine, and dose reduction is required in the setting of renal
dysfunction. The main site of action is inhibition of the DNA enzyme topoisomerase
II. Etoposide has clinical activity in germ cell cancer, small cell and
non-small cell lung cancer, Hodgkin’s and non-Hodgkin’s lym-phomas, and gastric
cancer. In addition, it is effective in high-dose regimens in the transplant
setting for breast cancer and lympho-mas. Major toxicities are listed in Table
54–4.
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