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针对无可用基因组变异的晚期非小细胞肺癌患者,铂类和免疫治疗之后,未来有哪些新趋势?

英文原题:What is on the Horizon Beyond Platinum and Immunotherapy for Patients With Advanced Non-Small Cell Lung Cancer Without Actionable Genomic Aberrations?

PubMed 2025/12/19(内容时间) JCO Oncol Pract Q1 · IF 5.5(JCR 2025)

研究概要

非小细胞肺癌(NSCLC)仍然是全球癌症相关死亡的主要原因。

中文摘要

非小细胞肺癌(NSCLC)仍是全球癌症相关死亡的首要原因。尽管靶向治疗和免疫治疗已改变了一线治疗格局,但大多数无可操作基因组变异(AGA)的患者将在初始治疗的第一年内出现疾病进展。在此,我们综述了针对无AGA的晚期NSCLC患者的关键临床试验、新兴策略、挑战及未满足的需求。多西他赛联合或不联合雷莫西尤单抗是含铂化疗和免疫治疗后进展患者的标准二线治疗。靶向治疗仅适用于具有特定AGA的患者。理解癌症免疫逃逸的标志性特征是在化疗免疫治疗之外开发新策略的关键。抗血管生成药物与免疫检查点抑制剂(ICIs)的联合在含铂治疗和ICI进展后显示出喜忧参半的结果。双特异性抗体,特别是ivonescimab,在这一领域显示出令人鼓舞的早期疗效。人工智能驱动的病理组学和影像组学工具可能有助于未来优化治疗选择。CAR-T 细胞疗法仍处于研究阶段。无AGA的晚期NSCLC患者在化疗免疫治疗后进展,治疗选择有限。特定抗体等新型疗法已显示出有前景的结果。未来的进展将取决于预测性生物标志物的开发以及对ICI耐药机制的理解,以指导药物研发。

展开英文摘要原文

Non-small cell lung cancer (NSCLC) remains the leading cause of cancer-related death worldwide. While targeted therapy and immunotherapy have transformed first-line management, most patients without actionable genomic alterations (AGAs) will experience disease progression within the first year of their initial treatment. Here, we review pivotal trials, emerging strategies, challenges, and unmet needs for patients with advanced NSCLC without AGAs. Docetaxel with or without ramucirumab is the standard second-line therapy for patients who have progressed after platinum-based chemotherapy and immunotherapy. Targeted therapy is only suitable for patients with specific AGAs. Understanding the hallmarks of cancer immune evasion is key to developing new strategies beyond chemoimmunotherapy. The combination of antiangiogenic agents with immune checkpoint inhibitors (ICIs) has shown mixed results after progression on platinum and ICI. Bispecific antibodies, particularly ivonescimab, have shown encouraging early efficacy in this space. Artificial intelligence-driven pathomics and radiomics tools may help to refine treatment selection in the future. Chimeric antigen receptor T-cell therapy remains investigational. Patients with advanced NSCLC without AGAs who progressed after chemoimmunotherapy have limited treatment options. Novel therapies such as specific antibodies have shown promising results. Future progress will depend on the development of predictive biomarkers and understanding the mechanisms of resistance to ICIs to guide drug development.

论文信息

作者
Ribeiro Rangel A、Cavalcante Lima Chagas G、Cavalcante Lima Chagas R、El Osta B
第一作者单位
Faculty of Medicine, Federal University of Ceará, Fortaleza, CE, Brazil.Brazil
通讯作者单位
Department of Hematology and Medical Oncology, Emory University School of Medicine, Winship Cancer Institute of Emory University, Atlanta, GA.United States
文献类型
综述
期刊
JCO oncology practice2026 Sep
原文标识
PubMed 41418081 · DOI 10.1200/OP-25-00936