Randomized comparison of etoposide pharmacokinetics after oral etoposide phosphate and oral etoposide

被引:20
作者
deJong, RS
Mulder, NH
Uges, DRA
Kaul, S
Winograd, B
Sleijfer, DT
Groen, HJM
Willemse, PHB
vanderGraaf, WTA
deVries, EGE
机构
[1] UNIV GRONINGEN HOSP,DEPT MED ONCOL,NL-9700 RB GRONINGEN,NETHERLANDS
[2] UNIV GRONINGEN HOSP,DEPT PHARM,NL-9700 RB GRONINGEN,NETHERLANDS
[3] BRISTOL MYERS SQUIBB PHARMACEUT RES INST,PRINCETON,NJ 08543
[4] BRISTOL MYERS SQUIBB PHARMACEUT RES INST,WALLINGFORD,CT
[5] UNIV GRONINGEN HOSP,DEPT PULMONOL,NL-9700 RB GRONINGEN,NETHERLANDS
关键词
etoposide; etoposide phosphate; oral; pharmacokinetics; toxicity;
D O I
10.1038/bjc.1997.282
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Etoposide phosphate is a water-soluble prodrug of etoposide. The plasma pharmacokinetics of etoposide following oral administration of etoposide phosphate or oral etoposide were compared. Seventeen patients with solid tumours were enrolled to receive oral etoposide phosphate 125 mg m(-2) on days 1-5 every 3 weeks, with escalation to 175 mg m(-2) from course 3 when possible. Patients were randomized to receive oral etoposide phosphate or oral etoposide on day 1 of course 1 and the alternative compound on day 1 of course 2. Fifteen patients received two or more courses and were evaluable for pharmacokinetic comparisons. The median AUC(inf) (area under the concentration vs time curve from zero to infinity) of etoposide was 77.7 mg l(-1) h after etoposide phosphate (95% CI 61.3-100.5) and 62.0 mg l(-1) h after oral etoposide (95% CI 52.2-76.9). The difference in favour of etoposide phosphate was borderline significant: median 9.9 mg l(-1) h (95% CI 0.1-32.8 mg l(-1) h; P = 0.05). However, the inter-patient variability of etoposide AUC(inf) was not improved (coefficients of variation 42.3% and 48.4%). Etoposide phosphate was undetectable in plasma after oral administration. Toxicities of oral etoposide phosphate were not different from those known for etoposide. In conclusion, oral etoposide phosphate does not offer a clinically relevant benefit over oral etoposide.
引用
收藏
页码:1660 / 1666
页数:7
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