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:Immunotherapy in Gastrointestinal Cancers.
免疫治疗在过去十年中彻底改变了癌症治疗。
免疫治疗在过去十年中彻底改变了癌症治疗。在一些既往面临终末期疾病的癌症患者群体中,可以实现长期持久的缓解。在本章中,我们总结了目前关于免疫治疗用于胃肠道癌症(食管鳞状细胞癌、食管胃腺癌、胰腺癌、胆道癌、肝细胞癌、结直肠癌和肛管鳞状细胞癌)的3期临床试验证据。我们讨论了临床试验中用于筛选最可能从免疫治疗中获益的患者的有意义生物标志物,例如错配修复缺陷(MMRd)/微卫星不稳定性(MSI)和程序性死亡配体-1(PD-L1)免疫组织化学(IHC)表达。关于免疫治疗在辅助/围手术期中的作用、对免疫治疗有应答的患者的最佳手术时机,以及胃肠道恶性肿瘤患者特有的毒性,临床问题正在出现。我们概述了免疫治疗在胃肠道癌症中的当前格局和未来前景,例如通过与其他检查点抑制剂、细胞毒性化疗、靶向药物、放疗、CAR-T疗法和癌症疫苗联合来提高检查点阻断疗效的策略。
Immunotherapy has revolutionised cancer treatment over the past decade. Long-term durable responses can be achieved in some cancer patient populations that were previously facing terminal disease. In this chapter, we summarise current phase 3 clinical trial evidence for the use of immunotherapy in gastrointestinal cancers (oesophageal squamous cell carcinoma, oesophago-gastric adenocarcinoma, pancreatic cancer, biliary cancer, hepatocellular carcinoma, colorectal cancer, and squamous cell cancer of the anus). We discuss meaningful biomarkers used in clinical trials to select patients most likely to benefit from immunotherapy, such as mismatch-repair deficiency (MMRd)/microsatellite instability (MSI) and programmed-death-ligand-1 (PD-L1) immunohistochemistry (IHC) expression. Clinical questions are arising regarding the role of immunotherapy in the adjuvant/perioperative setting, optimal timing of surgery in patients who respond to immunotherapy, and toxicities specific to patients with gastrointestinal malignancies. We outline the current landscape and future horizon of immunotherapy in gastrointestinal cancers, such as strategies to increase effectiveness of checkpoint blockade through combinations with other checkpoint inhibitors, cytotoxic chemotherapy, targeted agents, radiotherapy, CAR-T therapy, and cancer vaccines.
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