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拓扑替康与标准药物联合应用于患者人肿瘤细胞原代培养中的协同相互作用。

Synergistic interactions of combinations of topotecan with standard drugs in primary cultures of human tumor cells from patients.

作者信息

Jonsson E, Fridborg H, Nygren P, Larsson R

机构信息

Division of Clinical Pharmacology, Uppsala University Hospital, Sweden.

出版信息

Eur J Clin Pharmacol. 1998 Sep;54(7):509-14. doi: 10.1007/s002280050505.

Abstract

OBJECTIVE

Combination therapies are important in the treatment of many tumor types. This study was undertaken to find candidates for combination therapy with the novel topoisomerase I inhibitor topotecan.

METHODS

The cytotoxic effect of topotecan alone and in combination with five standard cytotoxic drugs was studied in 27 primary cultures of human tumor cells from patients with various diagnoses using the fluorometric microculture cytotoxicity assay (FMCA). The combinations were analysed according to the multiplicative concept of drug interaction.

RESULTS

The additive model was shown to be a better descriptor than the effect of the most effective agent (Dmax) for all drug combinations tested. Topotecan in combination with cisplatin (CisP) was the drug combination showing synergy in the highest percentage of samples (54%), followed by topotecan in combination with doxorubicin (Dox: 39%), etoposide (P16; 23%), paclitaxel in the formulation Taxol (22%) and cytarabine (AraC; 12%). The high percentage of synergistic interactions was especially pronounced in solid tumors. In 28% of the samples tested, drug sensitivity testing of only single drugs failed to predict response to the drugs in combination.

CONCLUSION

Cisplatin and doxorubicin showed promising effects in combination with topotecan, and clinical trials with these combinations seem warranted. The results also indicate the value of testing drug combinations in in vitro drug sensitivity testing.

摘要

目的

联合疗法在多种肿瘤类型的治疗中很重要。本研究旨在寻找与新型拓扑异构酶I抑制剂拓扑替康联合治疗的候选药物。

方法

使用荧光微量培养细胞毒性测定法(FMCA),对来自不同诊断患者的27种人肿瘤细胞原代培养物进行了拓扑替康单独及与五种标准细胞毒性药物联合使用时的细胞毒性作用研究。根据药物相互作用的相乘概念对联合用药进行分析。

结果

对于所有测试的药物组合,相加模型被证明比最有效药物的效应(Dmax)更能描述药物相互作用。拓扑替康与顺铂(CisP)联合使用时,在最高比例的样本中显示出协同作用(54%),其次是拓扑替康与阿霉素(Dox:39%)、依托泊苷(P16;23%)、紫杉醇制剂Taxol(22%)和阿糖胞苷(AraC;12%)联合使用。协同相互作用的高比例在实体瘤中尤为明显。在28%的测试样本中,仅单一药物的药敏试验无法预测联合用药的反应。

结论

顺铂和阿霉素与拓扑替康联合使用显示出有前景的效果,对这些联合用药进行临床试验似乎是有必要的。结果还表明了在体外药敏试验中测试药物联合使用的价值

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