Division of Surgery & Cancer, Imperial College London, Hammersmith Hospital, Du Cane Road, W12 0NN, London, UK.
University Hospital of Wales, Heath Park, Cardiff.
Future Oncol. 2024;20(36):2839-2847. doi: 10.1080/14796694.2024.2396795. Epub 2024 Sep 16.
Overactivation of the JAK/STAT pathway is one of the drivers for the pathophysiology of hepatocellular carcinoma (HCC). We propose a Phase Ib study to evaluate the safety and efficacy of itacitinib, a selective JAK1 inhibitor, as a second-line treatment for patients with advanced or metastatic HCC.Twenty-five patients will receive 400 mg itacitinib orally daily, 28-day cycle. Safety will be reviewed prior to each cycle. Tumor response assessed every 2 months until disease progression, death or withdrawal. Tumor biopsies and blood samples will be taken for presence of mutations.Activation of JAK/STAT pathway drives HCC development and is associated with immunotherapy resistance. Itacitinib is hypothesized to be safe and effective in HCC patients that have progressed after first-line therapies. EudraCT: 2017-004437-81 NCT04358185 (ClinicalTrials.gov).
JAK/STAT 通路的过度激活是肝细胞癌 (HCC) 病理生理学的驱动因素之一。我们提出了一项 Ib 期研究,以评估选择性 JAK1 抑制剂 itacitinib 作为晚期或转移性 HCC 二线治疗的安全性和疗效。25 名患者将接受 400mg 每日口服 itacitinib,28 天为一个周期。每个周期前将审查安全性。每 2 个月评估肿瘤反应,直至疾病进展、死亡或退出。将采集肿瘤活检和血液样本,以检测 突变的存在。JAK/STAT 通路的激活驱动 HCC 的发展,并与免疫治疗耐药性相关。假设 itacitinib 对一线治疗后进展的 HCC 患者是安全有效的。EudraCT:2017-004437-81 NCT04358185(ClinicalTrials.gov)。