CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Breaking bottlenecks: the future of hepatocellular carcinoma clinical trials and therapeutic targets.
Breaking bottlenecks: the future of hepatocellular carcinoma clinical trials and therapeutic targets.
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本研究分析并总结了 HCC 临床试验的概况以及治疗靶点的安全性和特异性,为 HCC 临床研究提供了参考。
为肝细胞癌(HCC)临床试验提供参考,研究者分析了 HCC 临床试验及治疗靶点。
使用 Informa 数据库分析全球及中国的 HCC 临床试验,继而考察 TACE、阿帕替尼及 CAR-T/NK 等新兴策略,并分析致癌生物标志物和治疗靶点。结合 HPA-RNA、HPA-Proteins 和 GTEx-RNA 数据集,对治疗靶点安全性进行联合分析;最后利用 HPA 病理学数据和 CPTAC 数据分析治疗靶点特异性及前景。
过去十年 HCC 临床试验迅速发展,但目前已进入瓶颈期,多数突破集中在联合治疗。中国和美国的试验数量居主导地位。TACE 联合全身治疗已成为中晚期 HCC 的有效治疗策略。阿帕替尼及 TACE 联合全身治疗是中国方案的特点;后者也主要在日本和美国开展。目前靶向免疫治疗占据主导,而 CAR-T/NK 仍处于早期阶段。多数治疗靶点与 VEGF 通路相关,间接证实 TKI-ICI 联合治疗在 HCC 中的主导作用。多数靶点安全性较低、特异性较差;但 RRM2、KDR 和 AURKA 具有较强安全性和特异性,靶向治疗前景优异。
本研究分析并总结了 HCC 临床试验概况以及治疗靶点的安全性和特异性,为 HCC 临床研究提供参考。
To provide a reference for hepatocellular carcinoma (HCC) clinical trials, we analyzed HCC clinical trials and therapeutic targets.
Using the Informa database, we analyzed the global and China HCC clinical trials. We then explored TACE, Apatinib, and emerging strategies (CAR T/NK). Additionally, we analyzed the oncogenic biomarkers and therapeutic targets. We conducted a joint analysis of therapeutic target safety using HPA-RNA, HPA-Proteins, and GTEx-RNA datasets. Finally, we analyzed the specificity and prospects of therapeutic targets using HPA pathology data and CPTAC data.
HCC clinical trials have developed rapidly over the past decade but have now reached a bottleneck, with most breakthroughs focusing on combination therapies. China and the USA dominate in the number of trials. TACE combined with systemic therapy has become an effective treatment strategy for intermediate to advanced HCC. Apatinib and TACE combined with systemic therapy are characteristic of China, while the latter is also mainly conducted in Japan and the USA. Currently, targeted immune therapies dominate the field, and CAR T/NK still in the early stages. Most therapeutic targets are related to the VEGF pathway, which indirectly confirms the predominant role of TKI-ICI combination therapy in HCC treatment. Most targets have low safety and poor specificity. However, RRM2, KDR, and AURKA have strong safety and specificity, showing excellent prospects for targeted HCC therapy.
This study analyzed and summarized the overview of HCC clinical trials and the safety and specificity of therapeutic targets, providing a reference for HCC clinical research.
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