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ZD1694(拓扑替康):一种新型胸苷酸合成酶抑制剂,对结直肠癌有活性。

ZD1694 (Tomudex): a new thymidylate synthase inhibitor with activity in colorectal cancer.

作者信息

Jackman A L, Farrugia D C, Gibson W, Kimbell R, Harrap K R, Stephens T C, Azab M, Boyle F T

机构信息

CRC Centre for Cancer Therapeutics, Institute of Cancer Research, Sutton, Surrey, UK.

出版信息

Eur J Cancer. 1995 Jul-Aug;31A(7-8):1277-82. doi: 10.1016/0959-8049(95)00166-g.

Abstract

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 rate on interim analysis) led to the current Phase III study, randomised against 5-fluorouracil/leucovorin.

摘要

ZD1694(拓扑替康)是一种新型抗叶酸剂,是胸苷酸合成酶(TS)的特异性抑制剂。有证据表明,ZD1694的活性谱在体外对结肠肿瘤的作用仅与5-氟尿嘧啶(亚叶酸调节)部分重叠。强大的细胞毒活性依赖于通过还原型叶酸/甲氨蝶呤细胞膜载体(RFC)主动摄取进入细胞,并随后代谢为多聚谷氨酸化形式(三、四和五聚谷氨酸)。这些多聚谷氨酸作为TS抑制剂的活性约高60倍,且不易从细胞中流出。在各种小鼠组织(如小肠上皮、肝脏和肾脏)中也会发生广泛的多聚谷氨酸化,导致高组织/血浆药物比,并持续较长时间。ZD1694在小鼠中有抗肿瘤活性,尽管该物种中高血浆胸苷会使以下情况复杂化:(1)治疗指数的解释;(2)可能观察到活性的肿瘤类型;以及(3)临床评估剂量和给药方案的转化。ZD1694进入了临床研究,并已完成I期和II期评估,在几种肿瘤类型中观察到了活性。II期结直肠癌研究中的显著活性(中期分析时客观缓解率为29%)促成了目前针对5-氟尿嘧啶/亚叶酸的III期随机对照研究。

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