Time-Dependent Pharmacokinetics of 5-Fluorouracil and Association With Treatment Tolerability in the Adjuvant Setting of Colorectal Cancer

被引:9
作者
Ibrahim, Toni [1 ]
Di Paolo, Antonello [2 ]
Amatori, Federica [2 ]
Mercatali, Laura [1 ]
Ravaioli, Elena [1 ]
Flamini, Emanuela [1 ]
Sacanna, Emanuele [1 ]
Del Tacca, Mario [2 ]
Danesi, Romano [2 ]
Amadori, Dino [1 ]
机构
[1] Ist Sci Romognolo Studio & Curo Tumori, Osteoncol Ctr, Meldola, Italy
[2] Univ Pisa, Dept Internal Med, Div Pharmacol & Chemotherapy, I-56126 Pisa, Italy
关键词
5-Fluorouracil; pharmacokinetics; metabolism; toxicity; GENE-EXPRESSION; DOSE ADJUSTMENT; SEVERE TOXICITY; FLUOROURACIL; CISPLATIN; CHEMOTHERAPY; RESISTANCE;
D O I
10.1177/0091270010396710
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The authors evaluated the influence of 5-fluorouracil (5-FU.) on treatment tolerability in 81 colorectal cancer patients given adjuvant 5-FU intravenously plus folinic acid for 6 cycles. The pharmacokinetics of 5-FU and its inactive metabolite 5-fluoro-5,6-dihydrouracil (5-FDHU) were measured on days 1 and 5 of the first chemotherapy cycle, 5 and 45 minutes after bolus administration. 5-FU clearance was significantly lower on day 5 (62.64 +/- 20.16 L/h/m(2)) than on day 1(74.83 +/- 31.61 L/h/m(2)). The lower 5-FU clearance values also predicted the side effects during the entire course of chemotherapy. In particular, patients with low clearance values on day 1 had a further reduction in this parameter on day 5, associated with severe toxicities. In conclusion, 5-FU alters its clearance, which could be partly due to a reduction in 5-FDHU biotransformation. These findings have safety implications for poor metabolizers whose drug clearance may fall below the threshold during repeated treatment cycles.
引用
收藏
页码:361 / 369
页数:9
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