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基于循环肿瘤DNA(ctDNA)的非小细胞肺癌微小残留病

Circulating tumor DNA (ctDNA)-based minimal residual disease in non-small cell lung cancer.

作者信息

Tang Libo, Li Ruiyang, Wen Huahai, Zhou Qing, Xu Chongrui

机构信息

School of Medicine, South China University of Technology, Guangzhou, Guangdong 510080, China.

Guangdong Lung Cancer Institute, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong 510080, China.

出版信息

Chin Med J Pulm Crit Care Med. 2023 Jun 28;1(4):207-214. doi: 10.1016/j.pccm.2023.04.001. eCollection 2023 Dec.

DOI:10.1016/j.pccm.2023.04.001
PMID:39171282
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11332816/
Abstract

Lung cancer is the second most common cancer worldwide and the leading cause of cancer-related fatalities, with non-small cell lung cancer (NSCLC) accounting for 85% of all lung cancers. Over the past forty years, patients with NSCLC have had a 5-year survival rate of only 16%, despite improvements in chemotherapy, targeted therapy, and immunotherapy. Circulating tumor DNA (ctDNA) in blood can be used to identify minimal residual disease (MRD), and ctDNA-based MRD has been shown to be of significance in prognostic assessment, recurrence monitoring, risk of recurrence assessment, efficacy monitoring, and therapeutic intervention decisions in NSCLC. The level of MRD can be obtained by monitoring ctDNA to provide guidance for more precise and personalized treatment, the scientific feasibility of which could dramatically modify lung cancer treatment paradigm. In this review, we present a comprehensive review of MRD studies in NSCLC and focus on the application of ctDNA-based MRD in different stages of NSCLC in current clinical practice.

摘要

肺癌是全球第二大常见癌症,也是癌症相关死亡的主要原因,其中非小细胞肺癌(NSCLC)占所有肺癌的85%。在过去四十年中,尽管化疗、靶向治疗和免疫治疗有所改善,但NSCLC患者的5年生存率仅为16%。血液中的循环肿瘤DNA(ctDNA)可用于识别微小残留病(MRD),基于ctDNA的MRD已被证明在NSCLC的预后评估、复发监测、复发风险评估、疗效监测和治疗干预决策中具有重要意义。通过监测ctDNA可以获得MRD水平,为更精确和个性化的治疗提供指导,其科学可行性可能会极大地改变肺癌治疗模式。在本综述中,我们对NSCLC中MRD的研究进行了全面综述,并重点关注基于ctDNA的MRD在当前临床实践中NSCLC不同阶段的应用。

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本文引用的文献

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Changes in Circulating Tumor DNA Reflect Clinical Benefit Across Multiple Studies of Patients With Non-Small-Cell Lung Cancer Treated With Immune Checkpoint Inhibitors.循环肿瘤 DNA 的变化反映了接受免疫检查点抑制剂治疗的非小细胞肺癌患者的多项研究中的临床获益。
JCO Precis Oncol. 2022 Aug;6:e2100372. doi: 10.1200/PO.21.00372.
2
Organ-specific efficacy in advanced non-small cell lung cancer patients treated with first-line single-agent immune checkpoint inhibitors.一线单药免疫检查点抑制剂治疗晚期非小细胞肺癌患者的器官特异性疗效。
Chin Med J (Engl). 2022 Jun 20;135(12):1404-1413. doi: 10.1097/CM9.0000000000002217.
3
Circulating Tumor DNA Kinetics Predict Progression-Free and Overall Survival in EGFR TKI-Treated Patients with EGFR-Mutant NSCLC (SWOG S1403).
循环肿瘤 DNA 动力学可预测 EGFR 突变 NSCLC 患者接受 EGFR-TKI 治疗的无进展生存期和总生存期(SWOG S1403)。
Clin Cancer Res. 2022 Sep 1;28(17):3752-3760. doi: 10.1158/1078-0432.CCR-22-0741.
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Characterization of Metastatic Non-Small Cell Lung Cancer and Oligometastatic Incidence in an Era of Changing Treatment Paradigms.描述转移非小细胞肺癌和寡转移发生率在不断变化的治疗模式时代。
Int J Radiat Oncol Biol Phys. 2022 Nov 15;114(4):603-610. doi: 10.1016/j.ijrobp.2022.04.050. Epub 2022 May 30.
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The clinical utility of dynamic ctDNA monitoring in inoperable localized NSCLC patients.动态循环肿瘤DNA监测在不可切除的局限性非小细胞肺癌患者中的临床应用价值
Mol Cancer. 2022 May 19;21(1):117. doi: 10.1186/s12943-022-01590-0.
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