随着二线治疗的进展,解决NSCLC进展中未满足的需求。

Q3 Medicine
Exploration of targeted anti-tumor therapy Pub Date : 2024-01-01 Epub Date: 2024-11-01 DOI:10.37349/etat.2024.00277
Kinsley Wang, Alexis Leyba, Robert Hsu
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引用次数: 0

摘要

肺癌是全球癌症死亡的主要原因,非小细胞肺癌(NSCLC)占85%。尽管免疫治疗和靶向治疗等一线治疗取得了进展,但对这些治疗的耐药性很常见,导致对有效二线治疗的需求显著未得到满足。本综述评估了晚期或转移性NSCLC目前和新兴的二线治疗方案,重点关注其疗效和改善患者预后的潜力。抗血管生成药物如ramucirumab联合化疗,特别是多西紫杉醇,已经显示出适度的成功。针对特定肿瘤抗原的抗体-药物偶联物(adc)为靶向治疗提供了一条有前景的途径,而嵌合抗原受体(CAR)-T细胞疗法和t细胞受体疗法利用患者的免疫系统更有效地对抗癌症。mRNA疫苗虽然处于早期阶段,但显示出诱导针对癌症特异性抗原的强大免疫反应的潜力。在此基础上,分子检测的最新进展和肿瘤微环境的探索开辟了新的治疗途径,进一步增强了非小细胞肺癌个性化二线治疗的潜力。虽然adc和双特异性抗体越来越受关注,但需要更精确的生物标志物来优化治疗反应。通过液体活检等技术进行定期监测,可以实时跟踪EGFR T790M等突变,从而及时调整治疗。此外,嗜中性粒细胞和巨噬细胞在肿瘤微环境中的作用越来越被认为是一种潜在的治疗途径,Smad3成为一个关键靶点。进一步研究药物测序、毒性管理和生物标志物开发对于改善非小细胞肺癌的治疗效果至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Addressing the unmet need in NSCLC progression with advances in second-line therapeutics.

Lung cancer is the leading cause of cancer mortality globally, with non-small cell lung cancer (NSCLC) accounting for 85% of cases. Despite advancements in first-line treatments such as immunotherapy and targeted therapies, resistance to these treatments is common, creating a significant unmet need for effective second-line therapies. This review evaluates current and emerging second-line therapeutic options for advanced or metastatic NSCLC, focusing on their efficacy and potential to improve patient outcomes. Anti-angiogenic drugs like ramucirumab combined with chemotherapy, particularly docetaxel, have shown moderate success. Antibody-drug conjugates (ADCs) targeting specific tumor antigens offer a promising avenue for targeted therapy, while chimeric antigen receptor (CAR)-T cell therapy and T-cell receptor therapy leverage the patient's immune system to combat cancer more effectively. mRNA vaccines, although in early stages, show potential for inducing robust immune responses against cancer-specific antigens. Building on this foundation, recent advancements in molecular testing and the exploration of the tumor microenvironment are opening new therapeutic avenues, further enhancing the potential for personalized second-line treatments in NSCLC. While ADCs and bispecific antibodies are gaining traction, more precise biomarkers are needed to optimize treatment response. Regular monitoring through techniques like liquid biopsies allows real-time tracking of mutations such as EGFR T790M, enabling timely therapeutic adjustments. Additionally, the role of neutrophils and macrophages in the tumor microenvironment is increasingly being recognized as a potential therapeutic avenue, with Smad3 emerging as a key target. Further research into drug sequencing, toxicity management, and biomarker development remains crucial to improving NSCLC treatment outcomes.

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来源期刊
CiteScore
2.80
自引率
0.00%
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审稿时长
13 weeks
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