为肝细胞癌武装 GPC3 CAR T 细胞:多少才足够,下一步是什么?
Armouring GPC3 CAR T cells for hepatocellular carcinoma: how much is enough and what comes next?
英文原题:Dendritic Cell-immunotherapy for Advanced Hepatocellular Carcinoma
这是一项 II 期注册临床试验,评估树突状细胞治疗肿瘤的安全性、可行性及初步疗效。当前状态:进行中(不再招募)。计划入组 100 例。试验地点:中国 · 桃园(共 1 个中心,其中中国 1 个)。登记号:NCT07726329。
不限性别 · ≥ 18 Years
纳入标准: • 晚期肝细胞癌(HCC),标准治疗无效;白细胞计数3,000–12,000/μL;血小板>80,000/μL;预期生存期>3个月;存在可测量肿瘤。 排除标准: • HIV感染;巴塞罗那临床肝癌分期(BCLC)相关排除情形;急性感染;脓毒症;其他晚期恶性肿瘤;急性肝衰竭。
Inclusion Criteria: * advanced HCC patients, no response to standard treatment; WBC : 3000-12000/ul; platelet: \>80000/ul; anticipated survival \> 3 months, measurable tumors. Exclusion Criteria: * HIV; BCLC stage; acute infection; sepsis; other advanced malignancy; acute liver failure;
以上为辅助阅读译文。是否适合入组须由主治医生判断,最终以登记平台与研究者确认为准。
主要终点:Incidence of Treatment-Related Adverse Events · To evaluate the safety of the treatments by assessing the number of participants with treatment-related adverse events. · up to 48 months.;Objective Tumor Response · To evaluate the tumor responses under the treatments as assessed by modified RECIST criteria. · From date of first treatment until the date of first documented progression, assessed up to 48 months.
次要终点:Overall Survival (OS);Enhancement of Immunity
II期,单一治疗组
晚期肝细胞癌预后较差。本研究中,符合条件的患者将接受肿瘤抗原负载的自体树突状细胞治疗,随后接受经导管动脉化疗栓塞(TACE)。研究终点为评估肿瘤反应和患者生存情况。
The prognosis of advanced hepatocellular carcinoma is poor. In this study, the eligible patients will be treated by tumor antigen-pulsed autologous dendritic cells and followed by TACE. The end points are to see tumor response and patient survival.
MEMBER ACCOUNT
登录成功会直接打开下一页。