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紫杉烷类药物在乳腺癌和卵巢癌治疗中的风险与益处。

Risks and benefits of taxanes in breast and ovarian cancer.

作者信息

Michaud L B, Valero V, Hortobagyi G

机构信息

Breast Oncology, Division of Pharmacy, The University of Texas M.D. Anderson Cancer Center, Houston 77030, Texas, USA.

出版信息

Drug Saf. 2000 Nov;23(5):401-28. doi: 10.2165/00002018-200023050-00005.

Abstract

The taxanes are a unique class of agents with a broad spectrum of clinical activity. They act by binding to tubulin, producing unnaturally stable microtubules and subsequent cell death. The distribution and elimination of paclitaxel depend on dose and administration rate. This nonlinearity is much less evident at lower infusion rates (24-hour infusions) and more evident at high plasma concentrations (3-hour infusions). The pharmacokinetics of docetaxel also suggest the presence of nonlinear pathways, but these appear to be clinically insignificant at the current doses utilised (60 to 100 mg/m2). Both agents undergo hepatic metabolism and biliary excretion and require dose adjustment in the setting of liver dysfunction. Drug interactions are quite common with these agents, some of which are sequence-dependent and clinically significant. The optimal dose of paclitaxel is not known at this time, and controversy over possible dose- or schedule-related differences in efficacy still remain. Docetaxel is somewhat more consistent in its dose and scheduling information, but controversy remains regarding a dose-benefit relationship as well as scheduling differences (weekly vs every 3 weeks). Toxicity profiles for these agents are somewhat different. Paclitaxel is more likely to be associated with peripheral neuropathy and myalgias/arthralgias than docetaxel. Docetaxel is more likely to be associated with a cumulative fluid retention syndrome that can be dose limiting. Paclitaxel and docetaxel are both highly active agents against breast cancer, including tumours that are resistant to anthracyclines. Docetaxel tends to have higher response rates overall, but direct comparisons at maximally tolerated doses have not been completed. Combination regimens with many different agents are attempting to improve on the responses seen with single-agent taxanes. The combination of paclitaxel and a platinum compound should be utilised as first-line therapy of advanced ovarian cancer. Controversy lies in the choice of the platinum compound and the dose and administration schedule of paclitaxel. Substitution of docetaxel for paclitaxel in these platinum-containing regimens is also being investigated. The taxanes also exhibit activity against ovarian cancer in patients previously exposed to platinum agents. These agents may also be administered intraperitoneally for local therapy of metastatic ovarian cancer. Although docetaxel and paclitaxel are often considered similar in activity and tolerability, this review emphasises the fact that these agents are indeed different. Clinicians need to be familiar with the benefits and adverse events related to each agent in order to make informed, appropriate clinical decisions.

摘要

紫杉烷类是一类具有广泛临床活性的独特药物。它们通过与微管蛋白结合发挥作用,产生异常稳定的微管并导致细胞死亡。紫杉醇的分布和消除取决于剂量和给药速率。这种非线性在较低输注速率(24小时输注)时不太明显,而在高血浆浓度(3小时输注)时更明显。多西他赛的药代动力学也提示存在非线性途径,但在目前使用的剂量(60至100mg/m²)下,这些途径在临床上似乎无显著意义。两种药物均经肝脏代谢和胆汁排泄,在肝功能不全时需要调整剂量。这些药物的药物相互作用很常见,其中一些具有顺序依赖性且在临床上具有重要意义。目前尚不清楚紫杉醇的最佳剂量,关于疗效方面可能存在的剂量或给药方案差异的争议仍然存在。多西他赛在剂量和给药方案信息方面较为一致,但关于剂量-效益关系以及给药方案差异(每周一次与每三周一次)的争议仍然存在。这些药物的毒性特征有所不同。与多西他赛相比,紫杉醇更易引起周围神经病变和肌痛/关节痛。多西他赛更易引起可能限制剂量的累积性液体潴留综合征。紫杉醇和多西他赛都是治疗乳腺癌的高效药物,包括对蒽环类药物耐药的肿瘤。总体而言,多西他赛的缓解率往往较高,但尚未完成最大耐受剂量下的直接比较。与许多不同药物的联合方案正在尝试改善单药紫杉烷类药物的疗效。紫杉醇与铂类化合物的联合应用应作为晚期卵巢癌的一线治疗方案。争议在于铂类化合物的选择以及紫杉醇的剂量和给药方案。在这些含铂方案中用多西他赛替代紫杉醇也正在研究中。紫杉烷类药物对先前接受过铂类药物治疗的卵巢癌患者也具有活性。这些药物也可通过腹腔内给药用于转移性卵巢癌的局部治疗。尽管多西他赛和紫杉醇通常在活性和耐受性方面被认为相似,但本综述强调了这两种药物确实存在差异这一事实。临床医生需要熟悉与每种药物相关的益处和不良事件,以便做出明智、恰当的临床决策。

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