Kanzawa F, Matsushima Y, Ishihara J, Shimizu E, Sasaki Y, Eguchi K, Shinkai T, Saijo N, Miyazawa N, Hamburger A W
J Pharmacobiodyn. 1986 Sep;9(9):715-21. doi: 10.1248/bpb1978.9.715.
One hundred and sixty-eight different specimens of human carcinoma of the lung were tested for in vitro drug sensitivity using the human tumor clonogenic assay (HTCA) originally described by Hamburger and Salmon. One hundred and twenty-two (73%) specimens grew adequately for chemosensitivity testing. Most tumors were resistant to chemotherapeutic drugs, but in vitro sensitivity, regardless of the type of drugs, varied markedly from specimen to specimen. Although response rates to individual drugs ranged between 9% and 23%, half the specimens tested were sensitive in vitro to at least one drug. A higher in vitro sensitivity rate was observed in small cell lung carcinoma (31%) than in non-small cell lung carcinoma (17%). The frequency of in vitro sensitivity was greater for patients who had received no prior chemotherapy than those who were in relapse. These in vitro results are similar to current clinical experience. There was a significant association between in vitro sensitivity of cells from a primary tumor as compared to its metastases. Overall HTCA appears to be useful in selecting appropriate chemotherapy for individual patients with carcinoma of the lung.
采用最初由汉堡和萨尔蒙描述的人肿瘤克隆形成试验(HTCA),对168份不同的人肺癌标本进行了体外药敏试验。122份(73%)标本生长良好,足以进行化疗敏感性测试。大多数肿瘤对化疗药物耐药,但体外敏感性,无论药物类型如何,在不同标本之间差异显著。尽管对个别药物的反应率在9%至23%之间,但所测试的标本中有一半在体外对至少一种药物敏感。小细胞肺癌的体外敏感率(31%)高于非小细胞肺癌(17%)。未接受过先前化疗的患者的体外敏感频率高于复发患者。这些体外结果与当前临床经验相似。原发性肿瘤细胞与其转移灶的体外敏感性之间存在显著关联。总体而言,HTCA似乎有助于为个体肺癌患者选择合适的化疗方案。