Tsai C M, Ihde D C, Kadoyama C, Venzon D, Gazdar A F
NCI-Navy Medical Oncology Branch, Bethesda, MD.
Eur J Cancer. 1990;26(11-12):1148-52. doi: 10.1016/0277-5379(90)90274-w.
In vitro drug sensitivity testing (DST) of long-term cultures from small cell lung cancer (SCLC) tumours was correlated with response and survival after four cycles of etoposide and cisplatin. 27 cell lines from 25 patients were tested by the semi-automated MTT assay after a median culture of 29 months. The logs of the IC50 concentrations for etoposide and cisplatin were correlated with each other. For both drugs, median IC50 values of patients with partial or complete responses ("responders") were significantly lower (7-8 fold) than those of non-responders. When survival was plotted according to whether drug IC50 values were in the upper or lower halves, curves for etoposide were significantly different, but those of cisplatin were not. DST of the long-term cell lines by MTT assay was significantly correlated with the Weisenthal dye exclusion assay of earlier passages of the same cell lines. DST of long-term SCLC cultures can predict clinical response and, for etoposide, survival. Disease-oriented panels of carefully selected, continuous, human tumour cell lines can be used to screen new drugs.
对小细胞肺癌(SCLC)肿瘤的长期培养物进行体外药物敏感性测试(DST),并将其与依托泊苷和顺铂四个周期后的反应及生存率相关联。在经过中位数为29个月的培养后,采用半自动MTT法对来自25例患者的27个细胞系进行了检测。依托泊苷和顺铂的IC50浓度对数相互关联。对于这两种药物,部分或完全缓解(“反应者”)患者的中位IC50值显著低于无反应者(7 - 8倍)。根据药物IC50值是否处于上半部分或下半部分绘制生存率曲线时,依托泊苷的曲线有显著差异,但顺铂的曲线无显著差异。通过MTT法对长期细胞系进行的DST与同一细胞系早期传代的魏森塔尔染料排除试验显著相关。对SCLC长期培养物进行DST可预测临床反应,对于依托泊苷还可预测生存率。精心挑选的、连续的人肿瘤细胞系组成的疾病导向性细胞库可用于筛选新药。