Perez E A, Buckwalter C A, Reid J P
Division of Hematology/Oncology, Mayo Clinic Jacksonville, FL 32224, USA.
Semin Oncol. 1996 Dec;23(6 Suppl 15):21-5.
Paclitaxel (Taxol; Bristol-Myers Squibb Company, Princeton, NJ) and etoposide are two chemotherapy agents with broad cytotoxic activity but different mechanisms of action and resistance. Previous in vitro studies of their combined cytotoxicity have yielded conflicting results. We evaluated the effects of drug scheduling in cell growth inhibition in lung and breast human cancer cell lines. A clonogenic assay with either simultaneous or sequential 24-hour incubation of paclitaxel and etoposide was used to assess growth inhibition, and the combination index was used to evaluate drug interactions. In these studies, including the A549 human lung cancer cell line, mild antagonism (combination index, > 1) was observed with concurrent exposure of paclitaxel and etoposide, but synergism (combination index, < 1) was observed when the drugs were incubated sequentially. In view of the wide range of antitumor activity of both paclitaxel and etoposide, and the potential importance and clinical impact of optimizing drug doses and schedules, we recently completed a phase I study with the following objectives: (1) to determine the maximum tolerated dose of paclitaxel given intravenously on day 10 after 10 days of oral etoposide and (2) to investigate the toxicity profile of this combination of agents. Three consecutive cohorts consisting of a total of 29 patients with various measurable or assessable tumors were treated with paclitaxel by intravenous infusion over 3 hours after receiving 10 days of etoposide 50 mg orally twice daily. Conclusions for this clinical study were that the combination was feasible and tolerable and had demonstrated antitumor activity in a group of mostly pretreated patients. The recommended doses for phase II studies were etoposide 50 mg twice daily for 10 days followed by paclitaxel 150 mg/m2 intravenously over 3 hours. A phase II study in patients with extensive small cell lung cancer, with appropriate translational studies, has been initiated.
紫杉醇(泰素;百时美施贵宝公司,新泽西州普林斯顿)和依托泊苷是两种具有广泛细胞毒性活性但作用机制和耐药性不同的化疗药物。此前关于它们联合细胞毒性的体外研究结果相互矛盾。我们评估了给药方案对人肺癌和乳腺癌细胞系细胞生长抑制的影响。采用对紫杉醇和依托泊苷进行24小时同时或序贯孵育的克隆形成试验来评估生长抑制情况,并使用联合指数来评估药物相互作用。在这些研究中,包括A549人肺癌细胞系,当紫杉醇和依托泊苷同时暴露时观察到轻度拮抗作用(联合指数,>1),但当药物序贯孵育时观察到协同作用(联合指数,<1)。鉴于紫杉醇和依托泊苷都具有广泛的抗肿瘤活性,以及优化药物剂量和给药方案的潜在重要性和临床影响,我们最近完成了一项I期研究,其目标如下:(1)确定在口服依托泊苷10天后第10天静脉注射紫杉醇的最大耐受剂量,以及(2)研究这种联合用药的毒性特征。连续三个队列共29例患有各种可测量或可评估肿瘤的患者,在每天口服两次50 mg依托泊苷10天后,接受3小时静脉输注紫杉醇治疗。该临床研究的结论是,这种联合用药是可行且可耐受的,并且在一组大多经过预处理的患者中已显示出抗肿瘤活性。II期研究的推荐剂量为依托泊苷每天两次50 mg,共10天,随后静脉注射紫杉醇150 mg/m²,持续3小时。一项针对广泛期小细胞肺癌患者的II期研究,并进行了适当的转化研究,已经启动。