University of California Los Angeles, Los Angeles, CA, United States.
J Hepatol. 2013 Dec;59(6):1271-7. doi: 10.1016/j.jhep.2013.07.029. Epub 2013 Aug 6.
BACKGROUND & AIMS: Sorafenib is the only therapy shown to improve overall survival in advanced hepatocellular carcinoma (HCC). Combination therapy targeting multiple signaling pathways may improve outcomes. This phase I study was designed to determine the maximum tolerated dose (MTD) of everolimus given with sorafenib 400mg twice daily in patients with advanced HCC of Child-Pugh class A liver function who were naive to systemic therapy.
Everolimus was initiated at 2.5mg once daily and increased per a Bayesian sequential dose-escalation scheme based on the dose-limiting toxicities experienced within the first 28 days of treatment. Adverse events were assessed continuously. Efficacy was evaluated using the best overall response rate per RECIST.
Thirty patients were enrolled; 25 were evaluable for MTD determination. One out of 12 patients treated with everolimus 2.5mg once daily and 6 out of 13 patients treated with everolimus 5.0mg once daily experienced a dose-limiting toxicity, most commonly thrombocytopenia (n=5). All patients experienced 1 adverse event, most commonly diarrhea (66.7%), hand-foot skin reaction (66.7%), and thrombocytopenia (50.0%). Best overall response was stable disease (62.5% and 42.9% in the 2.5-mg and 5.0-mg cohorts, respectively). Median time to progression and overall survival in the 2.5-mg cohort were 4.5 months and 7.4 months, respectively, and 1.8 months and 11.7 months, respectively, in the 5.0-mg cohort.
In patients with advanced HCC, the everolimus MTD in combination with standard-dose sorafenib was 2.5mg once daily. The inability to achieve a biologically effective everolimus concentration at the MTD precluded phase II study of this combination.
索拉非尼是唯一被证明能改善晚期肝细胞癌(HCC)总生存期的治疗方法。针对多种信号通路的联合治疗可能会改善预后。本研究旨在确定索拉非尼 400mg 每日两次与依维莫司联合应用于初治的 Child-Pugh 分级 A 肝功能的晚期 HCC 患者中的最大耐受剂量(MTD)。
依维莫司起始剂量为 1 天 1 次 2.5mg,并根据治疗最初 28 天内出现的剂量限制性毒性进行贝叶斯序贯剂量递增方案调整。连续评估不良反应。采用 RECIST 评估最佳总体缓解率来评估疗效。
共入组 30 例患者,25 例可评估 MTD。依维莫司 2.5mg 1 天 1 次治疗的 12 例患者中 1 例和依维莫司 5.0mg 1 天 1 次治疗的 13 例患者中 6 例发生剂量限制性毒性,最常见的是血小板减少(n=5)。所有患者均出现 1 次不良反应,最常见的是腹泻(66.7%)、手足皮肤反应(66.7%)和血小板减少(50.0%)。最佳总体缓解为疾病稳定(2.5mg 和 5.0mg 队列分别为 62.5%和 42.9%)。2.5mg 队列的中位无进展生存期和总生存期分别为 4.5 个月和 7.4 个月,5.0mg 队列分别为 1.8 个月和 11.7 个月。
在晚期 HCC 患者中,依维莫司联合标准剂量索拉非尼的 MTD 为 1 天 1 次 2.5mg。由于无法在 MTD 时达到有效的依维莫司浓度,因此无法进行该联合治疗的 II 期研究。