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New therapeutic options for chemotherapy-resistant metastatic breast cancer: the epothilones.

机译:化疗耐药的转移性乳腺癌的新治疗选择:埃博霉素。

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摘要

When taxanes were introduced as anticancer agents some 20 years ago, their broad spectrum of activity was striking and engendered renewed hope for cancer patients. However, they were not without their problems, including a susceptibility to drug resistance caused by the drug efflux pump protein, P-glycoprotein. The epothilones are a new class of chemotherapeutic agents that have a mechanism of action similar enough to the taxanes to retain their broad spectrum of activity, but different enough to escape the multidrug resistance caused by P-glycoprotein. These properties are especially promising for patients with metastatic breast cancer who have run out of therapeutic options as a result of multidrug resistance. Ixabepilone, a semi-synthetic analogue of epothilone B, has recently been granted US FDA approval for the treatment of chemotherapy-resistant advanced breast cancer. Approval was based on results from a phase III study of ixabepilone in combination with capecitabine, as well as phase II studiesof ixabepilone monotherapy. Significantly prolonged progression-free survival and increased objective response rates were demonstrated in the phase III study when ixabepilone was administered in combination with capecitabine compared with capecitabine alone. The phase II trials demonstrated robust antitumour activity with single-agent ixabepilone in women with metastatic breast cancer that was resistant to taxanes, anthracyclines and capecitabine. Early data from phase I trials of KOS-1584 and sagopilone are positive and suggest that these drugs may also develop into useful chemotherapeutic agents. Significant, but manageable, toxicities have been observed with the epothilones. In particular, neuropathy has led to the uneven and slower than expected clinical development of ixabepilone as optimal administration regimens were established. Some differences in tolerability profiles exist between the different analogues. Overall, it is expected that the epothilones will play an important role in the treatment of breast cancer and other tumour types.
机译:大约20年前,当紫杉烷类化合物作为抗癌剂被引入时,其广泛的活性令人震惊,并为癌症患者带来了新的希望。然而,它们并非没有问题,包括对药物外排泵蛋白P-糖蛋白引起的耐药性的敏感性。埃坡霉素是一类新的化学治疗剂,其作用机理与紫杉烷类化合物相似,足以保留其广泛的活性谱,但又足以逃避由P-糖蛋白引起的多药耐药性。这些特性对于因多药耐药性而已失去治疗选择的转移性乳腺癌患者特别有前途。埃博霉素B的半合成类似物伊沙贝比隆最近已获得美国FDA批准,用于治疗对化疗耐药的晚期乳腺癌。批准是基于ixabepilone联合卡培他滨的III期研究结果,以及ixabepilone单药治疗的II期研究结果。与单独使用卡培他滨相比,将伊沙贝比隆与卡培他滨联用时,III期研究显示,III期研究显着延长了无进展生存期,提高了客观缓解率。 II期试验证明,单药ixabepilone对转移性乳腺癌女性具有强大的抗肿瘤活性,对紫杉烷类,蒽环类和卡培他滨有抗药性。来自KOS-1584和sagopilone的I期试验的早期数据是肯定的,表明这些药物也可能发展为有用的化学治疗剂。已经发现埃坡霉素具有明显但可控的毒性。特别是,由于建立了最佳的给药方案,神经病导致依沙贝比隆的临床发展不平衡且缓慢。不同的类似物之间存在一些耐受性差异。总体而言,预计埃博霉素在乳腺癌和其他肿瘤类型的治疗中将发挥重要作用。

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