Summary
The pharmacokinetics and toxicity of two schedules of etoposide administration were studied in 19 patients suffering from metastatic non-small-cell lung cancer. Ten subjects received a 72-h continuous venous infusion (CVI) of 360 mg/m2 etoposide, and nine were given a daily dose of 120 mg/m2 for 3 consecutive days. In the two groups 80 mg/m2 cis-diamminedichloroplatinum (II) (CDDP) was infused on day 1. With CVI, the steadystate plasma concentration was reached 12–24 h after the start of the treatment. The plasma elimination rate showed a biexponential decay curve in both groups. No significant difference between total body clearance and the β-phase volume of distribution was noted between the two modalities of administration. No relationship was found between biological and pharmacokinetic parameters.
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This work was supported by a grant from the Comité Départemental de la Haute Garonne de la Ligue Nationale de Lutte Contre le Cancer
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Chatelut, E., Chevreau, C., Blancy, E. et al. Pharmacokinetics and toxicity of two modalities of etoposide infusion in metastatic non-small-cell lung carcinoma. Cancer Chemother Pharmacol 26, 365–368 (1990). https://doi.org/10.1007/BF02897295
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DOI: https://doi.org/10.1007/BF02897295