Goodin Susan
The Cancer Institute of New Jersey, New Brunswick, New Jersey, USA.
Am J Health Syst Pharm. 2008 May 15;65(10 Suppl 3):S10-5. doi: 10.2146/ajhp080089.
The epothilones are effective antitumor medications for patients with breast cancer, including patients who have been previously treated with or are resistant to anthracyclines or the taxanes.
With the best currently available therapies, the median survival time for patients with metastatic breast cancer is only 2-3 years, and many patients develop resistance to taxanes or other chemotherapy drugs. The epothilones are a novel class of antitumor medications, similar to the taxanes in some respects, but that also possess several advantages. Like taxanes, epothilones are believed to produce antitumor effects by binding to and stabilizing intracellular microtubules, which are essential in DNA replication and cell division. Several in vitro and animal studies have shown that the epothilones are more potent microtubule stabilizers than the taxanes, they are effective against cancer cell lines with high levels of drug resistance, and they induce the regression of taxane-resistant human tumors. Preclinical studies also have demonstrated synergistic increases in tumor cell killing when the epothilones are combined with other antitumor medications. Epothilone B (patupilone) has been evaluated in a series of phase I and II clinical trials, which demonstrated disease stabilization or objective responses in patients with a variety of cancers, including ovarian, prostate, breast, colon, stomach, and kidney cancers. This agent is currently being evaluated in phase III clinical trials. A second epothilone, ixabepilone, was recently approved by the FDA for the treatment of metastatic breast cancer. Ixabepilone was evaluated as monotherapy for the treatment of breast cancer in phase II clinical trials of previously untreated patients and in taxane-experienced and taxane-resistant disease. A phase III clinical trial demonstrated that the combination of ixabepilone and capecitabine was superior to capecitabine alone in heavily pretreated, taxane-resistant patients.
Ongoing clinical trials will continue to define the role of the epothilones in cancer therapy.
埃坡霉素是治疗乳腺癌患者的有效抗肿瘤药物,包括那些先前接受过蒽环类药物或紫杉烷类药物治疗或对其耐药的患者。
采用目前最佳的治疗方法,转移性乳腺癌患者的中位生存时间仅为2至3年,许多患者会对紫杉烷类药物或其他化疗药物产生耐药性。埃坡霉素是一类新型抗肿瘤药物,在某些方面与紫杉烷类药物相似,但也具有若干优势。与紫杉烷类药物一样,埃坡霉素被认为是通过与细胞内微管结合并使其稳定来产生抗肿瘤作用的,而细胞内微管在DNA复制和细胞分裂中至关重要。多项体外和动物研究表明,埃坡霉素比紫杉烷类药物更有效地稳定微管,对具有高度耐药性的癌细胞系有效,并且能使紫杉烷类药物耐药的人类肿瘤消退。临床前研究还表明,埃坡霉素与其他抗肿瘤药物联合使用时,在杀伤肿瘤细胞方面具有协同增效作用。埃坡霉素B(帕土匹隆)已在一系列I期和II期临床试验中进行了评估,这些试验证明该药物对包括卵巢癌、前列腺癌、乳腺癌、结肠癌、胃癌和肾癌在内的多种癌症患者具有病情稳定作用或客观缓解效果。该药物目前正在进行III期临床试验。第二种埃坡霉素,伊沙匹隆,最近已获美国食品药品监督管理局批准用于治疗转移性乳腺癌。在先前未接受过治疗的患者以及对紫杉烷类药物有治疗经验和耐药的疾病的II期临床试验中,伊沙匹隆被评估作为单一疗法治疗乳腺癌。一项III期临床试验表明,在经过大量治疗、对紫杉烷类药物耐药的患者中,伊沙匹隆与卡培他滨联合使用优于单独使用卡培他滨。
正在进行的临床试验将继续明确埃坡霉素在癌症治疗中的作用。