Agrez M V, Lieber M M
J Surg Oncol. 1983 Apr;22(4):269-72. doi: 10.1002/jso.2930220413.
The cells obtained from 138 tumor samples taken from 135 patients with colorectal malignancies were cultured in vitro in a soft agar colony formation assay similar to that of Salmon and colleagues [1]. Significant colony formation occurred for 63 (51%) of evaluable tumor cultures, 53 of which were also tested against chemotherapeutic agents in vitro. The median number of drugs tested per tumor was 15. Using 70% inhibition of colony formation as the criterion for significant drug-induced cytotoxicity, only 3/53 (6%) of the tumors were noted to be sensitive to any drug. When colony counts generated by initially plated small tumor cell aggregates were taken into account, 8/40 (20%) of the tumors were noted to be sensitive in vitro to one or more agents. Because of the low rate of drug sensitivity found with this in vitro assay, its current role in the prospective assignment of chemotherapeutic treatment for patients with colorectal carcinoma is somewhat limited.
从135例结肠直肠癌患者的138份肿瘤样本中获取的细胞,在体外进行软琼脂集落形成试验培养,方法与Salmon及其同事[1]的方法类似。在可评估的肿瘤培养物中,63份(51%)出现了显著的集落形成,其中53份还在体外进行了化疗药物测试。每个肿瘤测试药物的中位数为15种。以集落形成抑制70%作为显著药物诱导细胞毒性的标准,仅3/53(6%)的肿瘤对任何药物敏感。当考虑最初接种的小肿瘤细胞聚集体产生的集落计数时,8/40(20%)的肿瘤在体外对一种或多种药物敏感。由于这种体外试验发现的药物敏感性率较低,其目前在为结肠癌患者进行化疗前瞻性分配中的作用在一定程度上受到限制。