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:Revisiting targeted therapy and immunotherapy for advanced cholangiocarcinoma.
胆管癌(CCA)是一种罕见且侵袭性强的恶性肿瘤。
胆管癌(CCA)是一种罕见且侵袭性强的恶性肿瘤。过去几年,CCA 发病率有所上升。手术是唯一有效治疗,但仅适用于少数患者。晚期 CCA 通常采用综合治疗,主要依赖 gemcitabine 联合 cisplatin 化疗。过去十年,下一代测序技术的出现可用于鉴定 CCA 的重要分子特征,多项研究已证实不同 CCA 亚型具有独特遗传异常。靶向成纤维细胞生长因子受体(FGFR)、异柠檬酸脱氢酶(IDH)和表皮生长因子受体 2(EGFR2)是正在发展的靶向疗法。此外,研究表明免疫疗法在 CCA 中发挥重要作用。目前正在研究程序性细胞死亡蛋白 1(PD-1)抑制剂、CAR-T 细胞和肿瘤浸润白细胞(TIL)。研究显示,靶向治疗、免疫疗法和传统化疗在 CCA 中存在一定机制联系,联合应用可显著改善晚期 CCA 患者预后。本研究旨在综述 CCA 靶向治疗和免疫疗法的研究进展。
Cholangiocarcinoma (CCA) is a rare and aggressive type of malignant tumor. In the past few years, there has been an increase in the incidence of CCA. Surgery is the only effective treatment but is only suitable for a small percentage of patients. Comprehensive treatment is the normal therapy for terminal CCA patients, depending basically on gemcitabine and cisplatin combination chemotherapy. In the past decade, the emergence of next-generation sequencing technology can be used for the identification of important molecular features of CCA, and several studies have demonstrated that different CCA subtypes have unique genetic aberrations. Targeting fibroblast growth factor receptor (FGFR), isocitrate dehydrogenase (IDH) and epidermal growth factor receptor 2 (EGFR2) are emerging targeted therapies. In addition, researches have indicated that immunotherapy has a key function in CCA. There is ongoing research on programmed cell death protein 1 inhibitors (PD-1), chimeric antigen receptor T cells (CAR-T) and tumor-infiltrating leukocyte (TILs). Researches have shown that targeted therapy, immunotherapy, and conventional chemotherapy in CCA had certain mechanistic links, and the combination of those can greatly improve the prognosis of advanced CCA patients. This study aimed to review the research progress of targeted therapy and immunotherapy for CCA.
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