BOXED WARNING Administer under supervision of a physician experienced in cancer chemotherapy; severe myelosuppression with resulting infection or bleeding may occur
FDA dosing
Population
Start
Target
Max
Small cell lung cancer
Adults
Oral dose = 2× the IV dose rounded to nearest 50 mg (2×35 mg/m2/day ×4 days to 2×50 mg/m2/day ×5 days)
Modify for myelosuppressive combination drugs and prior RT/chemo
100 mg/m2/day ×5 days (2×50)
Renal Dose adjustment required in renal impairment — label defers specifics to PRECAUTIONS section (not in fetched text)
Hepatic Undefined
Repeat chemotherapy courses at 3–4 week intervals, after adequate recovery from toxicity
Instructions
Wear impervious gloves for all handling of blister packs (dermal-exposure risk)
Store capsules refrigerated 2–8°C
Handle/dispose as cytotoxic anticancer drug
Cautions
Myelosuppression is dose-related and dose-limiting: granulocyte nadir day 7–14, platelet nadir day 9–16, recovery by day 20; deaths reported
Secondary acute leukemia reported rarely with etoposide-containing regimens
Anaphylactic-like reactions (<1% with capsules), can be fatal
Adverse reactions
Leukopenia (<4,000 WBC: 60–91%)
Thrombocytopenia
Anemia
Nausea/vomiting (31–43%)
Anorexia
Diarrhea
Stomatitis/mucositis-esophagitis
Alopecia (up to 66%)
Peripheral neurotoxicity
Hypotension
Allergic reactions
Rare: SJS/TEN, optic neuritis, interstitial pneumonitis, hepatic toxicity at high doses