CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Post-immunotherapy second-line strategies for hepatocellular carcinoma: State of the art and ongoing trials.
Post-immunotherapy second-line strategies for hepatocellular carcinoma: State of the art and ongoing trials.
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肝细胞癌(HCC)的治疗格局在免疫检查点抑制剂(ICI)引入后发生了显著演变,ICI现已成为一线系统治疗的标准方案。然而,随着越来越多患者在基于ICI的联合治疗后出现疾病进展,最佳二线治疗策略仍未明确。目前获批的药物,如瑞戈非尼、卡博替尼和雷莫西尤单抗,尚未在ICI治疗后人群中专门进行测试,其在该背景下的疗效仍不确定。本综述对不可切除HCC患者在一线免疫治疗进展后的系统二线治疗策略进行了全面且批判性的分析。
我们总结了来自早期阶段研究和回顾性系列研究的现有证据,并描述了正在进行的临床试验的理论基础、疗效信号和开发状态。治疗手段包括酪氨酸激酶抑制剂、新型基于ICI的联合方案、双特异性抗体、T细胞疗法(CAR-T 细胞和T细胞受体T细胞),以及其他新兴策略如肝脏靶向前药和微生物群调节。尽管当前数据仍然有限,但多项试验正在进行中,反映了令人信服的生物学假说。其多样性凸显了这一治疗领域的复杂性和机遇。未来研究应聚焦于识别预测性生物标志物、优化安全性,以及制定个体化序贯策略,以改善这一快速扩大的患者群体的预后。
The treatment landscape of hepatocellular carcinoma (HCC) has significantly evolved following the introduction of immune checkpoint inhibitors (ICIs), which are now the standard of care in first-line systemic therapy.
However, as more patients experience progression after ICI-based combinations, the optimal second-line treatment strategy remains undefined. Currently approved agents, such as regorafenib, cabozantinib, and ramucirumab, have not been specifically tested in the post-ICI setting, and their efficacy in this context remains uncertain. This review provides a comprehensive and critical analysis of systemic second-line treatment strategies in patients with unresectable HCC after progression to frontline immunotherapy.
We summarize the available evidence from early-phase studies and retrospective series and describe the rationale, efficacy signals, and development status of ongoing clinical trials. Therapeutic approaches include tyrosine kinase inhibitors, novel ICI-based combinations, bispecific antibodies, T-cell therapies (chimeric antigen receptor-T and T-cell receptor-T), and other emerging strategies such as liver-targeted prodrugs and microbiota modulation.
While current data are still limited, several trials are ongoing and reflect compelling biological hypotheses. Their diversity highlights both the complexity and the opportunity of this therapeutic space. Future research should focus on identifying predictive biomarkers, optimizing safety, and developing individualized sequencing strategies to enhance outcomes in this rapidly expanding patient population.
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