Park C H, Amare M, Morrison F S, Maloney T R, Goodwin J W
Cancer Treat Rep. 1982 Jun;66(6):1257-61.
For 13 patients with acute nonlymphocytic leukemia receiving four-drug combination chemotherapy (14 chemotherapy trials), leukemic bone marrow cells were obtained before treatment and were exposed in vitro to all four-drug-mixture solutions simultaneously followed by the survival assessment of leukemic colony-forming cells (L-CFU). Survival of normal marrow colony-forming cells (CFU-C) was also assessed concurrently, and the sensitivity index (SI) of leukemic cells was determined as the ratio of the survival of CFU-C to that of L-CFU. Correlations of in vitro results to clinical results were excellent: four of five trials resulting in complete remission had high SI and eight of nine trials without complete remission had low SI (P = 0.02). The potential advantages of this method of exposing cells to drug mixture are discussed in terms of detecting drug synergism and improving the efficiency of in vitro chemotherapy sensitivity studies.
对于13例接受四联化疗的急性非淋巴细胞白血病患者(14次化疗试验),在治疗前获取白血病骨髓细胞,并将其同时体外暴露于四联混合药物溶液中,随后评估白血病集落形成细胞(L-CFU)的存活率。同时也评估正常骨髓集落形成细胞(CFU-C)的存活率,白血病细胞的敏感指数(SI)定义为CFU-C存活率与L-CFU存活率之比。体外结果与临床结果的相关性极佳:5次试验中有4次获得完全缓解,其SI较高;9次未获得完全缓解的试验中有8次SI较低(P = 0.02)。本文从检测药物协同作用和提高体外化疗敏感性研究效率的角度讨论了这种将细胞暴露于药物混合物方法的潜在优势。