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.
英文原题:Advances and challenges in immunotherapy for advanced esophageal squamous cell carcinoma.
Advances and challenges in immunotherapy for advanced esophageal squamous cell carcinoma.
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食管鳞状细胞癌(ESCC)是全球范围内高发且侵袭性强的恶性肿瘤,预后较差。多数患者确诊时已处于晚期,传统化疗疗效有限且常伴随显著毒性。近年来,免疫检查点抑制剂(ICIs),尤其是靶向PD-(L)1和CTLA-4的药物,已成为晚期ESCC一线及后线治疗的基石。
然而,仍存在显著的临床挑战,包括免疫耐药机制的复杂性、现有生物标志物预测效能欠佳、免疫相关不良事件(irAEs)管理困难,以及老年患者在临床试验中代表性不足。本综述总结了晚期ESCC免疫治疗的最新进展,评估了支持ICIs单药或与抗血管生成药物及酪氨酸激酶抑制剂等联合应用的临床证据。
进一步讨论了新型治疗方法的治疗潜力,包括双特异性抗体、CAR-T 细胞疗法和下一代ICIs,同时探讨了老年患者当前的治疗范式。强调了irAEs全面、纵向管理的重要性。
此外,本文深入分析了免疫耐药机制——如肿瘤新抗原丢失和关键信号通路失调——并批判性评价了现有生物标志物(包括PD-L1表达和肿瘤突变负荷(TMB))的局限性,以及生物标志物发现的新进展。
总之,尽管免疫治疗已显著改善晚期ESCC患者的预后并拓展了治疗前景,但仍需进一步研究以阐明耐药机制、优化治疗策略并识别可靠的预测性生物标志物。这些努力对于推进ESCC的精准医学并最终改善长期生存结局至关重要。
Esophageal squamous cell carcinoma (ESCC) is a highly prevalent and aggressive malignancy worldwide, associated with poor prognosis. Most patients are diagnosed at an advanced stage, where conventional chemotherapy offers limited therapeutic efficacy and is often accompanied by substantial toxicity. In recent years, immune checkpoint inhibitors (ICIs), particularly those targeting PD-(L)1 and CTLA-4, have emerged as cornerstone therapies in both first-line and subsequent treatment settings for advanced ESCC. Nevertheless, significant clinical challenges persist, including the complexity of mechanisms underlying immune resistance, suboptimal predictive performance of existing biomarkers, difficulties in the management of immune-related adverse events (irAEs), and underrepresentation of elderly patients in clinical trials.
This review summarizes recent advances in immunotherapy for advanced ESCC, evaluating the clinical evidence supporting ICIs as monotherapy or in combination with agents such as anti-angiogenic drugs and tyrosine kinase inhibitors. It further discusses the therapeutic potential of novel approaches, including bispecific antibodies, CAR-T cell therapy, and next-generation ICIs, while addressing current treatment paradigms for elderly patients. The importance of comprehensive, longitudinal management of irAEs is emphasized.
Additionally, this article provides an in-depth analysis of mechanisms contributing to immune resistance-such as loss of tumor neoantigens and dysregulation of key signaling pathways-and critically appraises the limitations of established biomarkers, including PD-L1 expression and tumor mutational burden (TMB), alongside emerging developments in biomarker discovery.
In conclusion, while immunotherapy has significantly improved outcomes and expanded therapeutic prospects for patients with advanced ESCC, further research is required to elucidate resistance mechanisms, refine treatment strategies, and identify robust predictive biomarkers. These efforts are essential to advance precision medicine in ESCC and ultimately enhance long-term survival outcomes.
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