Hortobagyi G N
Department of Breast Medical Oncology, University of Texas M.D. Anderson Cancer Center Houston, USA.
Oncology (Williston Park). 1997 Mar;11(3 Suppl 2):29-37.
Clinical trials to develop paclitaxel (Taxol)-containing combinations started in 1992 with several approaches to combine doxorubicin and paclitaxel. Schedule-dependent toxicity limited doses in the initial trials, although antitumor activity was high. More recently, a well-tolerated, highly effective doxorubicin/paclitaxel regimen was developed with the use of bolus anthracycline administration and a 3-hour infusion of paclitaxel. Combinations of paclitaxel with cisplatin have provided mixed results. Paclitaxel combined with fluorouracil (5-FU) and folinic acid proved effective in patients with extensive prior chemotherapy; the addition of mitoxantrone (Novantrone) to this combination was feasible, well tolerated, and possibly enhanced the efficacy of paclitaxel and 5-FU. Combinations of paclitaxel with cyclophosphamide (Cytoxan, Neosar), vinorelbine (Navelbine), edatrexate, and radiation continue in clinical development.
含紫杉醇(泰素)联合方案的临床试验始于1992年,有几种将阿霉素与紫杉醇联合的方法。尽管抗肿瘤活性很高,但在最初的试验中,剂量依赖性毒性限制了用药剂量。最近,通过推注蒽环类药物和3小时输注紫杉醇,开发出了一种耐受性良好、高效的阿霉素/紫杉醇方案。紫杉醇与顺铂联合的结果不一。紫杉醇联合氟尿嘧啶(5-FU)和亚叶酸对先前接受过广泛化疗的患者有效;在此联合方案中加入米托蒽醌(诺维本)是可行的,耐受性良好,并且可能增强了紫杉醇和5-FU的疗效。紫杉醇与环磷酰胺(环磷酰胺、异环磷酰胺)、长春瑞滨(诺维本)、依达曲沙和放疗联合的方案仍在临床研究中。