Bennett J A, Gruft H, McKneally M F, Zelterman D, Crispen R G
Cancer Res. 1983 Sep;43(9):4183-90.
Various measures of biological activity were studied in batches of lyophilized Tice Bacillus Calmette-Guérin (BCG) that have been used intrapleurally as adjuvant therapy in surgically resected Stage I lung cancer patients by our own group, the North American Lung Cancer Study Group, and the Ludwig Lung Cancer Study Group. The biological activities of BCG that were studied were: (a) inhibition of solid tumor growth in mice following s.c. inoculation of BCG admixed with methylcholanthrene-induced fibrosarcoma cells (MC 43); (b) protection against tumor colonization of lungs and prolongation of survival in mice pretreated intrapleurally with BCG and later inoculated i.v. with a lethal dose of MC 43 tumor cells; and (c) growth properties in vitro, including a determination of the relative amounts of growing and nongrowing material and the sensitivity of growing material to inhibition by isoniazid. Significant differences in biological activity among batches of BCG were found. Some batches of BCG protected mice against circulating tumor cells, while others did not. Batches of BCG which protected mice against circulating tumor cells were found to have greater sensitivity to isoniazid and higher viability than batches which did not elicit this antitumor activity. There were also trends of some batches of BCG outperforming others in the clinic. Cumulative disease-free interval of patients was longer with batches which protected mice against circulating tumor cells than with batches which did not protect mice against circulating tumor cells. The results of this study suggest that preclinical testing of BCG for antitumor activity may improve the efficacy of this agent in future clinical trials.
我们小组、北美肺癌研究小组和路德维希肺癌研究小组,对一批冻干的蒂策卡介苗(BCG)的多种生物活性指标进行了研究。这些冻干BCG曾作为辅助治疗手段,用于接受手术切除的I期肺癌患者的胸膜内注射。所研究的BCG生物活性包括:(a)皮下接种与甲基胆蒽诱导的纤维肉瘤细胞(MC 43)混合的BCG后,对小鼠实体瘤生长的抑制作用;(b)对经胸膜内注射BCG预处理、随后静脉注射致死剂量MC 43肿瘤细胞的小鼠,保护其肺部免受肿瘤定植并延长生存期;(c)体外生长特性,包括测定生长和非生长物质的相对含量,以及生长物质对异烟肼抑制作用的敏感性。结果发现,不同批次的BCG在生物活性上存在显著差异。部分批次的BCG能保护小鼠免受循环肿瘤细胞侵害,而其他批次则不能。与未引发这种抗肿瘤活性的批次相比,能保护小鼠免受循环肿瘤细胞侵害的BCG批次,对异烟肼更敏感,活力也更高。在临床上,部分批次的BCG也有优于其他批次的趋势。与不能保护小鼠免受循环肿瘤细胞侵害的批次相比,能保护小鼠免受循环肿瘤细胞侵害的批次,患者的累积无病间期更长。本研究结果表明,对BCG进行抗肿瘤活性的临床前检测,可能会提高该药物在未来临床试验中的疗效。