ZD1694 (TOMUDEX) - A NEW THYMIDYLATE SYNTHASE INHIBITOR WITH ACTIVITY IN COLORECTAL-CANCER

被引:109
作者
JACKMAN, AL [1 ]
FARRUGIA, DC [1 ]
GIBSON, W [1 ]
KIMBELL, R [1 ]
HARRAP, KR [1 ]
STEPHENS, TC [1 ]
AZAB, M [1 ]
BOYLE, FT [1 ]
机构
[1] ZENECA PHARMACEUT, MACCLESFIELD, CHESHIRE, ENGLAND
关键词
ZD1694; THYMIDYLATE SYNTHASE; POLYGLUTAMATION;
D O I
10.1016/0959-8049(95)00166-G
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ZD1694 (Tomudex) is a new antifolate which is a specific inhibitor of thymidylate synthase (TS). Evidence suggests that ZD1694 has a spectrum of activity that only partially overlaps with 5-fluorouracil (modulated with leucovorin) against colon tumours in vitro. Potent cytotoxic activity is dependent upon active uptake into cells via the reduced folate/methotrexate cell membrane carrier (RFC) and subsequent metabolism to polyglutamated forms (tri, tetra and pentaglutamates). These polyglutamates are approximately 60-fold more active as TS inhibitors and are not effluxed readily from cells. Extensive polyglutamation also occurs in various mouse tissues (e.g. small intestinal epithelium, liver and kidney), resulting in high tissue/plasma drug ratios which persist for a prolonged period. ZD1694 has antitumour activity in mice, although the high plasma thymidine in this species complicates: (1) the interpretation of therapeutic index; (2) tumour types in which activity is likely to be observed; and (3) translation of doses and schedules for clinical evaluation. ZD1694 entered clinical study and has completed Phase I and II evaluation, with activity observed in several tumour types. Appreciable activity in the Phase II colorectal study (29% objective response fate on interim analysis) led to the current Phase III study, randomised against 5-fluorouracil/leucovorin.
引用
收藏
页码:1277 / 1282
页数:6
相关论文
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