Goodin Susan
Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Piscataway, USA.
Am J Health Syst Pharm. 2008 Nov 1;65(21):2017-26. doi: 10.2146/ajhp070628.
The pharmacology, pharmacokinetics, clinical efficacy, safety, dosage, and administration of ixabepilone in patients with metastatic breast cancer are examined.
The clinical utility of the three main classes of chemotherapeutic agents used in breast cancer (i.e., anthracyclines, taxanes, and fluorinated pyrimidines) is limited in some patients by the emergence of drug resistance which leads to disease progression. A recent addition to the available drugs for the treatment of advanced breast cancer is the epothilone B analog ixabepilone, which has demonstrated clinical activity in patients who have tumors that have progressed while on other chemotherapy regimens, including anthracyclines and taxanes. In Phase II clinical trials of ixabepilone in patients with metastatic breast cancer, clinically meaningful benefits have been achieved with ixabepilone monotherapy in patients in whom anthracyclines, taxanes, and capecitabine are no longer effective. Ixabepilone has demonstrated activity in first-, second-, and subsequent-lines of therapy and in different subtypes of patients with advanced disease. In a Phase III trial in patients who had previously received taxanes and anthracyclines, the combination of ixabepilone and capecitabine was significantly more effective in producing an objective response and in prolonging progression-free survival than capecitabine alone. At the recommended dose and administration schedule, ixabepilone is generally well tolerated. The most clinically relevant adverse events associated with its use have been myelosuppression and peripheral neuropathy, which is primarily sensory and cumulative but reversible within six weeks of a dosage reduction or the discontinuation of therapy.
Ixabepilone, the first drug in a new class of microtubule-stabilizing agents called epothilones, offers a new treatment option for patients with metastatic or locally advanced breast cancer who are refractory to standard chemotherapy.
研究伊沙匹隆用于转移性乳腺癌患者的药理作用、药代动力学、临床疗效、安全性、剂量及用法。
乳腺癌治疗中使用的三类主要化疗药物(即蒽环类、紫杉烷类和氟嘧啶类)在一些患者中因出现耐药性导致疾病进展,其临床效用有限。用于治疗晚期乳腺癌的可用药物中,最近新增了埃坡霉素B类似物伊沙匹隆,它在接受包括蒽环类和紫杉烷类在内的其他化疗方案治疗时肿瘤仍进展的患者中显示出临床活性。在伊沙匹隆治疗转移性乳腺癌患者的II期临床试验中,对于蒽环类、紫杉烷类和卡培他滨不再有效的患者,伊沙匹隆单药治疗取得了具有临床意义的疗效。伊沙匹隆在一线、二线及后续治疗以及晚期疾病的不同亚型患者中均显示出活性。在一项针对先前接受过紫杉烷类和蒽环类治疗的患者的III期试验中,伊沙匹隆与卡培他滨联合使用在产生客观缓解和延长无进展生存期方面比单独使用卡培他滨显著更有效。在推荐剂量和给药方案下,伊沙匹隆总体耐受性良好。与其使用相关的最具临床相关性的不良事件是骨髓抑制和周围神经病变,后者主要为感觉性且具有累积性,但在剂量减少或停药六周内可逆转。
伊沙匹隆是一类名为埃坡霉素的新型微管稳定剂中的首个药物,为对标准化疗难治的转移性或局部晚期乳腺癌患者提供了一种新的治疗选择。