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DX-8951f与拓扑替康对新分离的成人及儿童人肿瘤细胞形成肿瘤集落的影响比较。

Comparison of DX-8951f and topotecan effects on tumor colony formation from freshly explanted adult and pediatric human tumor cells.

作者信息

Lawrence R A, Izbicka E, De Jager R L, Tohgo A, Clark G M, Weitman S D, Rowinsky E K, Von Hoff D D

机构信息

CTRC Research Foundation, Institute for Drug Development, San Antonio, TX 78245, USA.

出版信息

Anticancer Drugs. 1999 Aug;10(7):655-61. doi: 10.1097/00001813-199908000-00005.

Abstract

DX-8951f, which shows great therapeutic potential, was tested in the human tumor cloning system in adult and pediatric tumor types against which topotecan has been active. In 47 tumors from adults, DX-8951f had definite cytotoxic activity in a concentration-dependent manner with both 1 h and continuous exposures. Topotecan was minimally effective using a 1 h exposure and showed concentration-dependent inhibition with continuous exposure. In head-to-head comparisons at 1 h exposure against adult tumors, DX-8951f was significantly more effective at 0.1 and 1.0 microg/ml than topotecan. In head-to-head comparisons (continuous exposure), 1.0 microg/ml DX-8951f was more effective than topotecan at 1.0 microg/ml in adult tumors, including three of four head and neck, one of two kidney, two of five liver, six of 10 non-small cell lung, five of eight ovarian, four of eight prostate tumors, and in single specimens of breast, mesothelioma, colon and small cell lung tumors. With continuous exposure, DX-8951f and topotecan were equally effective at equimolar concentrations. The maximum tolerated dose for DX-8951f is 3 times that of topotecan, so higher doses of DX-8951f could be administered to patients. DX-8951f is a promising new antineoplastic agent with significant activity against tumors taken directly from patients.

摘要

DX - 8951f具有巨大的治疗潜力,已在成人和儿童肿瘤类型的人类肿瘤克隆系统中针对拓扑替康有效的肿瘤进行了测试。在47例成人肿瘤中,DX - 8951f在1小时暴露和持续暴露时均呈浓度依赖性地具有明确的细胞毒活性。拓扑替康在1小时暴露时效果甚微,持续暴露时呈浓度依赖性抑制。在针对成人肿瘤的1小时暴露的直接比较中,DX - 8951f在0.1和1.0微克/毫升时比拓扑替康显著更有效。在直接比较(持续暴露)中,1.0微克/毫升的DX - 8951f在成人肿瘤中比1.0微克/毫升的拓扑替康更有效,包括四例头颈部肿瘤中的三例、两例肾脏肿瘤中的一例、五例肝脏肿瘤中的两例、十例非小细胞肺癌中的六例、八例卵巢肿瘤中的五例、八例前列腺肿瘤中的四例,以及乳腺癌、间皮瘤、结肠癌和小细胞肺癌的单个标本。持续暴露时,DX - 8951f和拓扑替康在等摩尔浓度下效果相同。DX - 8951f的最大耐受剂量是拓扑替康的3倍,因此可以给患者施用更高剂量的DX - 8951f。DX - 8951f是一种有前景的新型抗肿瘤药物,对直接取自患者的肿瘤具有显著活性。

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