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:The Evolving Role of Immune-Checkpoint Inhibitors in Malignant Pleural Mesothelioma.
恶性胸膜间皮瘤(MPM)是一种罕见癌症,通常由石棉暴露引起,且预后极差。
恶性胸膜间皮瘤(MPM)是一种罕见癌症,通常由石棉暴露引起,预后极差。十余年间没有新治疗选择,而免疫检查点抑制剂(ICI)已证实优于标准化疗,并在一线及后线治疗中改善总生存期。然而,仍有相当比例患者无法从ICI中获益,凸显了开发新治疗策略和应答预测生物标志物的必要性。目前,化学免疫治疗联合方案或ICI联合抗VEGF疗法正在临床试验中评估,并可能在不久的将来改变标准治疗。另一些非ICI免疫疗法,如靶向间皮素的CAR-T细胞或树突状细胞疫苗,在早期临床试验中显示出有希望的结果,目前仍在开发中。最后,少数可手术患者围手术期使用ICI免疫疗法也正在评估。本综述旨在讨论免疫疗法在恶性胸膜间皮瘤管理中的当前作用及有前景的未来治疗方向。
Malignant pleural mesothelioma (MPM) is a rare cancer usually caused by asbestos exposure and associated with a very poor prognosis. After more than a decade without new therapeutic options, immune checkpoint inhibitors (ICIs) demonstrated superiority over standard chemotherapy, with improved overall survival in the first and later-line settings. However, a significant proportion of patients still do not derive benefit from ICIs, highlighting the need for new treatment strategies and predictive biomarkers of response. Combinations with chemo-immunotherapy or ICIs and anti-VEGF are currently being evaluated in clinical trials and might change the standard of care in the near future. Alternatively, some non-ICI immunotherapeutic approaches, such as mesothelin targeted CAR-T cells or denditric-cells vaccines, have shown promising results in early phases of trials and are still in development. Finally, immunotherapy with ICIs is also being evaluated in the peri-operative setting, in the minority of patients presenting with resectable disease. The goal of this review is to discuss the current role of immunotherapy in the management of malignant pleural mesothelioma, as well as promising future therapeutic directions.
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