Suppr超能文献

挑战难治性疾病——为小细胞肺癌开发分子驱动的治疗方法。

Challenging the recalcitrant disease-developing molecularly driven treatments for small cell lung cancer.

机构信息

Lung Unit, Royal Marsden Hospital, Downs Road, Sutton, Surrey, SM2 5PT, UK.

Drug Development Unit, Royal Marsden/Institute of Cancer Research, Downs Road, Sutton, Surrey, SM2 5PT, UK.

出版信息

Eur J Cancer. 2019 Sep;119:132-150. doi: 10.1016/j.ejca.2019.04.037. Epub 2019 Aug 21.

Abstract

Small cell lung cancer (SCLC) has been described as a 'recalcitrant' disease characterised by poor survival and with little progress made in developing novel treatments in the last decades. However, recent drug developments have opened some potential therapeutic avenues. In this review, the genomic landscape of SCLC is explored, in particular the Notch pathway and attempts to target the key node DLL3. The likely primary importance of MYC to SCLC subtype transformation and recent attempts to drug MYC are discussed. Bcl-2 is a druggable protein, highly expressed in SCLC, and relevant Bcl-2 targeting drugs are reviewed. None of these drug targets are, however, as advanced their development as the field of immunotherapy for SCLC. The key developments in single agent PD-L1 and PD-1 inhibitors and in combination with chemotherapy have led to the only recent licencing approvals for SCLC in recent years and will likely pave the way for future rational drug combinations. Drug development in SCLC poses its own challenges with rapid clinical deterioration often precluding trial entry. Effective drug development in a biomarker-driven approach depends on early patient screening and use of circulating biomarkers. Given recent developments, we may hope to be at the start of an era of greater progress in the treatment of SCLC.

摘要

小细胞肺癌(SCLC)被描述为一种“难治”的疾病,其生存情况较差,在过去几十年中,在开发新的治疗方法方面几乎没有取得进展。然而,最近的药物开发为一些潜在的治疗途径开辟了道路。在这篇综述中,探讨了 SCLC 的基因组景观,特别是 Notch 途径和靶向关键节点 DLL3 的尝试。讨论了 MYC 对 SCLC 亚型转化的可能主要重要性,以及最近尝试药物靶向 MYC 的情况。Bcl-2 是一种可药物治疗的蛋白质,在 SCLC 中高度表达,并且对相关的 Bcl-2 靶向药物进行了综述。然而,这些药物靶点都没有像免疫疗法那样在 SCLC 领域得到如此先进的发展。单药 PD-L1 和 PD-1 抑制剂的关键进展以及与化疗联合应用,导致近年来 SCLC 仅获得了最近的许可批准,并且可能为未来的合理药物联合治疗铺平道路。SCLC 的药物开发存在自身的挑战,快速的临床恶化往往使患者无法进入临床试验。在生物标志物驱动的方法中进行有效的药物开发取决于早期的患者筛选和使用循环生物标志物。鉴于最近的发展,我们可能希望处于 SCLC 治疗取得更大进展的时代的开始。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验