决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Hepatocellular carcinoma systemic treatment update: From early to advanced stage.
Hepatocellular carcinoma systemic treatment update: From early to advanced stage.
肝细胞癌(HCC)是全球第六大常见恶性肿瘤,但却是癌症相关死亡的第三大原因。
肝细胞癌(HCC)在全球最常见恶性肿瘤中排名第六,但在癌症相关死亡原因中排名第三。过去二十年,HCC 的全身治疗取得了重大突破,改善了治疗结局。除多种酪氨酸激酶抑制剂(mTKIs)外,免疫检查点抑制剂(ICIs)和抗血管生成药物也越来越多地被应用。由于显著的缓解率,ICI 联合抗血管生成药物或双 ICI 已成为新的标准治疗。然而,目前可用的全身治疗方案主要保留用于某些不适合局部区域治疗获益的中期和晚期患者。支持全身治疗作为早期 HCC 患者新辅助或辅助治疗的证据仍然有限,尤其是在根治性治疗后复发风险高的患者中。本综述梳理了全身治疗的最新进展,包括 mTKIs 和 ICIs,并考虑了关于一线和二线治疗结果、新辅助和辅助治疗背景中的作用以及与局部区域治疗联合的结果。本文还总结了关于全身治疗作用以及早期、中期和晚期 HCC 患者潜在新靶点的多项正在进行的临床试验,并揭示全身治疗不再局限于晚期 HCC。此外,T 细胞重定向策略的引入,包括双特异性抗体和CAR-T 细胞,已经彻底改变了 HCC 的治疗格局。未来研究应侧重于深入探索肿瘤屏障建立的机制。
Hepatocellular carcinoma (HCC) ranks the sixth most common malignancy but the third leading cause of cancer-related mortality in the world. Significant breakthroughs have been made in systemic treatment for HCC over the past two decades, which have improved treatment outcomes. In addition to multiple tyrosine kinase inhibitors (mTKIs), immune checkpoint inhibitors (ICIs) and antiangiogenic drugs are increasingly being applied. The combination of ICI and antiangiogenic or dual ICIs has become the new standard of care due to remarkable response rates. However, currently available systemic regimens are primarily reserved for certain patients in the intermediate and advanced stages who will not benefit from locoregional treatments. Evidence supporting the use of systemic treatment as neoadjuvant or adjuvant therapies in patients with early-stage HCC, especially the high risk of recurrence after curative treatments, remains limited. This review identified recent developments in systemic therapy, including mTKIs and ICIs, considering results on first- and second-line treatment, role of neoadjuvant and adjuvant settings, and combination with loco-regional therapy. Various ongoing clinical trials regarding the role of systemic therapies and potential novel targets in patients with early-, intermediate-, and advanced-stage HCC were also summarized and revealed that systemic therapy is no longer limited to advanced-stage HCC. Moreover, the introduction of T-cell redirecting strategies, including bispecific antibodies and chimeric antigen receptor T cells, has revolutionized the treatment landscape for HCC. Future research should focus on an in-depth exploration of the mechanisms governing the establishment of tumor barriers.
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