Medical Oncology Clinic, Institut Jules Bordet, Université Libre de Bruxelles , Brussels , Belgium.
Expert Rev Anticancer Ther. 2014 Jun;14(6):649-65. doi: 10.1586/14737140.2014.920693.
In the new era of 'precision' cancer medicine, new drug development has shifted from cytotoxic chemotherapy to molecularly targeted agents. Eribulin mesylate, a microtubule-destabilizing agent, is the only 'classical' cytotoxic agent approved for the treatment of breast cancer in the last 7 years. This synthetic analogue of halichondrin B, isolated from the marine sponge 'Halicondria Okaida', was responsible for prolonging overall survival of heavily pretreated metastatic breast cancer patients in a large Phase III trial. Eribulin is now under clinical development in earlier settings such as the neo-adjuvant and adjuvant settings. Furthermore, its unique mechanism of action and the absence of cross-resistance with taxanes have led to the design of clinical trials in multiple indications: bladder cancer, lung cancer, prostate cancer… The main adverse events are neutropenia, fatigue and peripheral neuropathy.
在“精准”肿瘤医学的新时代,新药研发已从细胞毒性化疗转向分子靶向药物。甲磺酸艾日布林是一种微管破坏剂,是过去 7 年来唯一获准用于乳腺癌治疗的“经典”细胞毒性药物。这种从海洋海绵“Halicondria Okaida”中分离出的海鞘素 B 的合成类似物,在一项大型 III 期试验中使经大量预处理的转移性乳腺癌患者的总生存期延长。甲磺酸艾日布林目前正在新辅助和辅助治疗等早期治疗环境中进行临床开发。此外,其独特的作用机制和与紫杉烷类药物无交叉耐药性,导致在多种适应症中进行了临床试验:膀胱癌、肺癌、前列腺癌……主要不良反应为中性粒细胞减少、疲劳和周围神经病变。