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:Targeting claudin 18.2 in gastric cancer: a review of emerging biologic agents.
CLDN18.2 靶向治疗已证明靶向非致癌驱动因素的治疗可行性,代表胃癌治疗范式的转变。
引言:zolbetuximab是首个靶向claudin 18.2(CLDN18.2)的单克隆抗体,已获批用于HER2阴性且CLDN18.2阳性的胃癌或胃食管结合部癌患者的一线治疗,为此前从分子靶向治疗或免疫检查点抑制剂中获益有限的患者带来了新的希望。 综述范围:本文介绍关键III期试验未能充分涵盖的临床认识,考察zolbetuximab诱发胃炎的临床病理特征以及治疗过程中CLDN18.2表达的动态变化。文章还探讨患者选择标准化、胃肠道毒性管理和治疗顺序优化等关键临床挑战,并概述新一代CLDN18.2靶向策略的最新进展,包括抗体药物偶联物、双特异性抗体和CAR-T细胞疗法。 专家观点:CLDN18.2靶向治疗证明了靶向非致癌驱动因子的治疗可行性,代表胃癌治疗范式的转变。抗体药物偶联物、双特异性抗体和CAR-T细胞疗法等新一代治疗方式,即使在CLDN18.2表达较低的患者中也已显示疗效,提示其有望扩大适用人群。未来,深入理解CLDN靶向治疗相关的胃肠道毒性、阐明耐药机制并制定合理的联合治疗策略,将是最大程度提升CLDN18.2阳性胃癌患者治疗获益的关键。
INTRODUCTION: Zolbetuximab, the first monoclonal antibody targeting claudin 18.2 (CLDN18.2), is approved as first-line treatment for patients with HER2-negative and CLDN18.2-positive gastric or gastroesophageal junction cancers, offering new hope to patients who previously derived limited benefit from molecular targeted therapies or immune checkpoint inhibitors. AREAS COVERED: This review presents clinical insights not fully captured in pivotal phase III trials, examining the clinicopathological characteristics of zolbetuximab-induced gastritis and the dynamics of CLDN18.2 expression during treatment. It further explores key clinical challenges - including standardized patient selection, management of gastrointestinal toxicities, and optimization of treatment sequencing - while providing an overview of recent advances in next-generation CLDN18.2-targeted strategies such as antibody - drug conjugates, bispecific antibodies, and CAR-T cell therapies. EXPERT OPINION: CLDN18.2-targeted therapy has demonstrated the therapeutic feasibility of targeting non-oncogenic drivers, representing a paradigm shift in gastric cancer treatment. Next-generation modalities such as ADCs, bispecific antibodies, and CAR-T cell therapies have shown efficacy even in patients with lower CLDN18.2 expression, suggesting potential to expand treatment eligibility. Moving forward, deeper understanding of gastrointestinal toxicities associated with CLDN-targeted therapies, elucidation of resistance mechanisms, and development of rational combination strategies will be essential to maximize therapeutic benefit in patients with CLDN18.2-positive gastric cancer.
MEMBER ACCOUNT
登录成功会直接打开下一页。