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:From biology to therapy: current standards and emerging strategies in pleural mesothelioma.
胸膜间皮瘤(PM)是一种侵袭性恶性肿瘤,治疗选择有限,长期预后差。
胸膜间皮瘤(PM)是一种侵袭性恶性肿瘤,治疗选择有限,长期预后差。几十年来,以铂类为基础的化疗一直是大多数患者的标准治疗。尽管对PM基因组改变的解读引发了对间皮瘤生物学和靶向治疗的重新关注,但这些尚未进入临床实践。近年来引入的nivolumab联合ipilimumab的双重免疫检查点阻断(ICB)标志着PM治疗数十年来首个重大进展,然而,许多患者对这些药物无应答,持久的长期缓解仍然罕见。目前,一系列替代治疗模式正在PM中进行临床研究,包括抗体药物偶联物、双特异性抗体、CAR-T 细胞、癌症疫苗和溶瘤病毒。本文综述了PM生物学理解方面的最新进展,并评估了旨在改善该疾病治疗的相关I-III期临床试验。我们还重点介绍了正在进行的和未来的临床试验,其中包含有前景的PM治疗候选方案。
Pleural mesothelioma (PM) is an aggressive malignancy with limited therapeutic options and poor long-term prognosis. Platinum-based chemotherapy has been the standard-of-care for most patients for decades. While the decoding of the genomic alterations in PM has triggered renewed interest in mesothelioma biology and targeted therapies, these have yet to reach clinical practice. The recent introduction of dual immune checkpoint blockade (ICB) with nivolumab plus ipilimumab has marked the first major advance in PM treatment for decades, yet, many patients do not respond to these drugs and durable long-term responses remain rare. A range of alternative treatment modalities are currently under clinical investigation in PM, including antibody-drug conjugates, bi-specific antibodies, chimeric antigen receptor T-cells, cancer vaccines, and oncolytic viruses. Here we review recent progress in the understanding of PM biology and evaluate relevant phase I-III clinical trials aimed at improving treatment for this disease. We also highlight ongoing and future clinical trials with promising candidates for PM therapy.
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