Harvard Medical School, Boston, MA 02115, USA.
Massachusetts General Hospital Cancer Center, Boston, MA 02114, USA.
Future Oncol. 2019 Jan;15(3):231-239. doi: 10.2217/fon-2018-0597. Epub 2018 Oct 26.
Lurbinectedin is an inhibitor of active transcription of protein-coding genes, causing DNA-break accumulation, apoptosis and modulation of the tumor microenvironment. Early-phase clinical trials indicate promising activity of lurbinectedin in small-cell lung cancer. Here, we describe the rationale and design of ATLANTIS (NCT02566993), an open-label, randomized, multicenter Phase III study to compare the efficacy of lurbinectedin and doxorubicin combination with standard-of-care chemotherapy, investigator's choice of cyclophosphamide/doxorubicin/vincristine or topotecan, in patients with small-cell lung cancer that has progressed following one line of platinum-based chemotherapy. Patients are randomized in a 1:1 ratio. The primary end point is overall survival and key secondary end points include progression-free survival, best tumor response and duration of response, each assessed by independent review committee.
鲁比卡丁是一种蛋白编码基因转录活性的抑制剂,可导致 DNA 断裂积累、细胞凋亡,并调节肿瘤微环境。早期临床研究表明,鲁比卡丁在小细胞肺癌中具有良好的活性。在这里,我们描述了 ATLANTIS(NCT02566993)的基本原理和设计,这是一项开放标签、随机、多中心的 III 期研究,旨在比较鲁比卡丁联合多柔比星与标准治疗化疗(研究者选择环磷酰胺/多柔比星/长春新碱或拓扑替康)在一线铂类化疗后进展的小细胞肺癌患者中的疗效。患者按 1:1 的比例随机分组。主要终点是总生存期,关键次要终点包括无进展生存期、最佳肿瘤缓解率和缓解持续时间,均由独立审查委员会评估。