The University of Texas MD Anderson Cancer Center, Department of Breast Medical Oncology, Houston, TX 77030, USA.
Dana-Farber Cancer Institute, Center for Women's Cancers, Boston, MA 02215, USA.
Future Oncol. 2019 Jul;15(19):2211-2225. doi: 10.2217/fon-2019-0180. Epub 2019 May 10.
The increasing incidence of breast cancer brain metastases is a major clinical problem with its associated poor prognosis and limited treatment options. The long-acting topoisomerase-1 inhibitor, etirinotecan pegol, was designed to preferentially accumulate in tumor tissue including brain metastases, providing sustained cytotoxic SN38 levels. Motivated by improved survival findings from subgroup analyses from the Phase III BEACON trial, this ongoing randomized, Phase III trial compares etirinotecan pegol to drugs commonly used for advanced breast cancer in patients with stable, treated breast cancer brain metastases who have been previously treated with an anthracycline, taxane and capecitabine. The primary end point is overall survival. Secondary end points include objective response rate, progression-free survival and time to CNS disease progression or recurrence in patients with/without CNS lesions present at study entry. Trial registration number: NCT02915744.
乳腺癌脑转移的发病率不断上升,是一个主要的临床问题,其预后不良且治疗选择有限。长效拓扑异构酶-1 抑制剂伊立替康聚乙二醇旨在优先积聚在肿瘤组织中,包括脑转移瘤,提供持续的细胞毒性 SN38 水平。基于 III 期 BEACON 试验亚组分析中改善的生存结果,这项正在进行的随机、III 期试验比较了伊立替康聚乙二醇与常用于晚期乳腺癌的药物,用于治疗有稳定、已治疗脑转移的乳腺癌患者,这些患者之前已接受过蒽环类药物、紫杉烷类药物和卡培他滨治疗。主要终点是总生存期。次要终点包括客观缓解率、无进展生存期以及有/无脑内病变患者的中枢神经系统疾病进展或复发时间。试验注册号:NCT02915744。