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一项研究索拉非尼联合依维莫司治疗晚期肝细胞癌的 I 期临床研究。

Phase I study investigating everolimus combined with sorafenib in patients with advanced hepatocellular carcinoma.

机构信息

University of California Los Angeles, Los Angeles, CA, United States.

出版信息

J Hepatol. 2013 Dec;59(6):1271-7. doi: 10.1016/j.jhep.2013.07.029. Epub 2013 Aug 6.

Abstract

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景与目的

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)。

方法

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。

结果

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。

结论

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。

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