Teplinsky Eleonora, Herzog Thomas J
a Don Monti Division of Hematology & Medical Oncology , Hofstra Northwell School of Medicine, Monter Cancer Center , Lake Success , NY , USA.
b Paul & Carolyn Flory Endowed Professor , University of Cincinnati Cancer Institute , Cincinnati , OH , USA.
Expert Opin Pharmacother. 2017 Feb;18(3):313-323. doi: 10.1080/14656566.2017.1285282.
The majority of women with epithelial ovarian cancer present with advanced stage disease and there is a critical need for novel drugs and treatment strategies to improve outcomes. Trabectedin is a unique cytotoxic agent with a complex mechanism of action. It binds to guanines in the N2 position in the minor groove of DNA and its cytotoxicity involves DNA repair pathways and transcription regulation. Trabectedin's activity is also related to the drug-induced changes of the tumor microenvironment. It has been shown to improve progression-free survival in combination with pegylated liposomal doxorubicin in patients with platinum-sensitive relapsed ovarian cancer. The most common adverse events experienced with trabectedin are nausea, vomiting, fatigue, neutropenia and transaminitis. Studies of biomarkers that are predictors of trabectedin benefit are underway. Areas covered: This review covers trabectedin's mechanism of action and pharmacology, the clinical development of the drug in ovarian cancer, ongoing trials, and the use of biomarkers to predict efficacy to trabectedin. Expert opinion: Ongoing phase III trials with biomarker studies will help to elucidate the patient population that will best benefit from trabectedin and pave the way for personalized treatment decisions and potential future approval of trabectedin in the United States.
大多数上皮性卵巢癌女性患者就诊时已处于疾病晚期,因此迫切需要新的药物和治疗策略来改善治疗效果。曲贝替定是一种独特的细胞毒性药物,作用机制复杂。它与DNA小沟中N2位置的鸟嘌呤结合,其细胞毒性涉及DNA修复途径和转录调控。曲贝替定的活性还与药物诱导的肿瘤微环境变化有关。在铂敏感复发性卵巢癌患者中,已证明曲贝替定与聚乙二醇化脂质体阿霉素联合使用可改善无进展生存期。使用曲贝替定最常见的不良事件是恶心、呕吐、疲劳、中性粒细胞减少和转氨酶升高。目前正在进行关于曲贝替定疗效预测生物标志物的研究。涵盖领域:本综述涵盖曲贝替定的作用机制和药理学、该药物在卵巢癌中的临床开发、正在进行的试验以及使用生物标志物预测曲贝替定疗效。专家意见:正在进行的伴有生物标志物研究的III期试验将有助于阐明最能从曲贝替定中获益的患者群体,并为个性化治疗决策以及曲贝替定未来在美国的潜在获批铺平道路。