Vahdat Linda
Breast Cancer Research Program, Weill Medical College of Cornell University, 425 E. 61st, 8th Floor, New York, NY 10065, USA.
Oncologist. 2008 Mar;13(3):214-21. doi: 10.1634/theoncologist.2007-0167.
Tumor resistance to chemotherapeutic agents ultimately leads to treatment failure in the majority of cancer patients. The identification of new agents that are less susceptible to mechanisms of tumor resistance could, therefore, bring significant clinical benefits to patients with advanced cancer. One new drug class of great interest in this respect is the epothilones and their analogues, which are microtubule inhibitors with low susceptibility to several mechanisms of drug resistance. Ixabepilone is an analogue of natural epothilone B with activity against a wide range of tumor types, including drug-resistant tumors. This is consistent with the preclinical activity of ixabepilone against human cancer cell lines resistant to taxanes and other agents. Taxane resistance in these cells may be acquired or primary and results from several mechanisms, such as overexpression of multidrug-resistance proteins and the betaIII-tubulin isoform. Ixabepilone has demonstrated efficacy as monotherapy or in combination with capecitabine in anthracycline- and taxane-pretreated/resistant metastatic breast cancer (MBC), and has recently been approved for use in resistant/refractory MBC. Other epothilones, such as patupilone, KOS-1584, and ZK-EPO, are also being evaluated in drug-resistant cancers. Ixabepilone represents a new treatment option for MBC patients with cancers resistant to available chemotherapeutic agents.
肿瘤对化疗药物产生耐药性最终会导致大多数癌症患者治疗失败。因此,鉴定对肿瘤耐药机制不太敏感的新型药物可能会给晚期癌症患者带来显著的临床益处。在这方面备受关注的一类新型药物是埃坡霉素及其类似物,它们是微管抑制剂,对多种耐药机制的敏感性较低。伊沙匹隆是天然埃坡霉素B的类似物,对多种肿瘤类型具有活性,包括耐药肿瘤。这与伊沙匹隆对耐紫杉烷和其他药物的人癌细胞系的临床前活性一致。这些细胞中的紫杉烷耐药性可能是获得性的或原发性的,由多种机制导致,如多药耐药蛋白和βIII-微管蛋白异构体的过表达。伊沙匹隆已证明作为单药治疗或与卡培他滨联合用于蒽环类和紫杉烷预处理/耐药的转移性乳腺癌(MBC)有效,并且最近已被批准用于耐药/难治性MBC。其他埃坡霉素,如帕土匹隆、KOS-1584和ZK-EPO,也正在耐药癌症中进行评估。伊沙匹隆为对现有化疗药物耐药的MBC患者提供了一种新的治疗选择。