Ichihashi H, Sako T, Akiyama S
Gan To Kagaku Ryoho. 1985 Aug;12(8):1560-5.
For use in routine clinical studies, modifications to Salmon and Hamburger's human tumor stem cell assay were made. A multiplate with 24 wells made the handling of a large number of samples feasible. The addition of anticancer drugs to the bottom layer of agar facilitated avoidance of exposure to drugs before cell plating and evaluation of the effect of long-acting drugs such as 5-fluorouracil. Storage of test plates including anticancer drugs in a freezer produced no loss of colony-forming activity. Specimens from 32 patients with advanced malignancies of the GI tract were tested for sensitivity to anticancer drugs. Forty-seven percent formed enough colonies for the performance of drug testing. Two patients showed sensitivity to drugs from both in vitro and in vivo results; the ascites in one disappeared while the other showed more than 50 percent regression of hepatic metastatic foci after treatment with suitable drugs. Nine patients showed resistance to drugs from both in vitro and in vivo results. Eight showed resistance to all tested drugs.
为用于常规临床研究,对萨尔蒙和汉堡的人类肿瘤干细胞检测方法进行了改进。一个带有24个孔的多孔板使处理大量样本成为可能。在琼脂底层添加抗癌药物有助于避免细胞接种前接触药物,并能评估5-氟尿嘧啶等长效药物的效果。将包含抗癌药物的测试板储存在冰箱中,集落形成活性没有损失。对32例胃肠道晚期恶性肿瘤患者的标本进行了抗癌药物敏感性测试。47%的标本形成了足够的集落用于药物测试。两名患者的体外和体内结果均显示对药物敏感;一名患者的腹水消失,另一名患者在用合适药物治疗后肝转移灶消退超过50%。九名患者的体外和体内结果均显示对药物耐药。八名患者对所有测试药物均耐药。