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小细胞肺癌的当前及未来治疗方法

Current and future therapies for small cell lung carcinoma.

作者信息

Zhai Xiaoqian, Zhang Zhengkun, Chen Yuxin, Wu Yanmou, Zhen Cheng, Liu Yu, Lin Yiyun, Chen Chong

机构信息

Department of Medical Oncology, State Key Laboratory of Biotherapy and Cancer Center and National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University, No. 1, Keyuan 4th Road, Gaopeng Avenue, Chengdu, 610041, Sichuan, China.

Lung Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China.

出版信息

J Hematol Oncol. 2025 Apr 1;18(1):37. doi: 10.1186/s13045-025-01690-6.

Abstract

Small cell lung cancer (SCLC) is an aggressive malignancy characterized by rapid proliferation and high metastatic potential. It is characterized by universal inactivation of and RB1, overexpression of the MYC family and dysregulation of multiple oncogenic signaling pathways. Among different patients, SCLCs are similar at the genetic level but exhibit significant heterogeneity at the molecular level. The classification of SCLC has evolved from a simple neuroendocrine (NE)/non-neuroendocrine (non-NE) classification system to a transcription factor-based molecular subtype system; lineage plasticity adds further complexity and poses challenges for therapeutic development. While SCLC is initially sensitive to platinum-based chemotherapy, resistance develops rapidly, leading to a dismal prognosis. Various antibodies, including PD-1/PD-L1 inhibitors and antibody‒drug conjugates, have been introduced into clinical practice or are being evaluated in clinical trials. However, their therapeutic benefits for SCLC patients remain limited. This review summarizes SCLC carcinogenic mechanisms, tumor heterogeneity, and the immune microenvironment of SCLC, with a focus on recent advances in metastasis and resistance mechanisms. Additionally, the corresponding clinical progress in tackling these challenges is discussed.

摘要

小细胞肺癌(SCLC)是一种侵袭性恶性肿瘤,其特点是增殖迅速且转移潜能高。它的特征是RB1普遍失活、MYC家族过表达以及多个致癌信号通路失调。在不同患者中,SCLC在基因水平上相似,但在分子水平上表现出显著的异质性。SCLC的分类已从简单的神经内分泌(NE)/非神经内分泌(非NE)分类系统演变为基于转录因子的分子亚型系统;谱系可塑性增加了进一步的复杂性,并给治疗开发带来挑战。虽然SCLC最初对铂类化疗敏感,但耐药性迅速发展,导致预后不佳。各种抗体,包括PD-1/PD-L1抑制剂和抗体-药物偶联物,已被引入临床实践或正在临床试验中进行评估。然而,它们对SCLC患者的治疗益处仍然有限。本综述总结了SCLC的致癌机制、肿瘤异质性和SCLC的免疫微环境,重点关注转移和耐药机制的最新进展。此外,还讨论了应对这些挑战的相应临床进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9745/11959764/b9f957426c3f/13045_2025_1690_Fig1_HTML.jpg

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