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本文引用的文献

1
Implementation of the 9th TNM for lung cancer: practical insights for radiologists.第九版肺癌TNM分期系统的应用:放射科医生的实践见解
Eur Radiol. 2025 Jan 17. doi: 10.1007/s00330-024-11345-8.
2
The prognostic value of radiogenomics using CT in patients with lung cancer: a systematic review.CT 影像组学在肺癌患者中的预后价值:一项系统评价
Insights Imaging. 2024 Oct 28;15(1):259. doi: 10.1186/s13244-024-01831-4.
3
Management of Non-Metastatic Non-Small Cell Lung Cancer (NSCLC) with Driver Gene Alterations: An Evolving Scenario.具有驱动基因改变的非转移性非小细胞肺癌(NSCLC)的管理:不断变化的情况。
Curr Oncol. 2024 Aug 30;31(9):5121-5139. doi: 10.3390/curroncol31090379.
4
Applications of CT-based radiomics for the prediction of immune checkpoint markers and immunotherapeutic outcomes in non-small cell lung cancer.基于 CT 的放射组学在非小细胞肺癌中预测免疫检查点标志物和免疫治疗结果的应用。
Front Immunol. 2024 Aug 22;15:1434171. doi: 10.3389/fimmu.2024.1434171. eCollection 2024.
5
The Proposed Ninth Edition TNM Classification of Lung Cancer.肺癌第九版 TNM 分期系统。
Chest. 2024 Oct;166(4):882-895. doi: 10.1016/j.chest.2024.05.026. Epub 2024 Jun 15.
6
Alectinib in Resected -Positive Non-Small-Cell Lung Cancer.阿来替尼治疗可切除阳性非小细胞肺癌。
N Engl J Med. 2024 Apr 11;390(14):1265-1276. doi: 10.1056/NEJMoa2310532.
7
Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.2022 年全球癌症统计数据:全球 185 个国家和地区 36 种癌症的发病率和死亡率全球估计数。
CA Cancer J Clin. 2024 May-Jun;74(3):229-263. doi: 10.3322/caac.21834. Epub 2024 Apr 4.
8
Hepatotoxicity in patients with non-small cell lung cancer treated with sotorasib after prior immunotherapy: a comprehensive clinical and pharmacokinetic analysis.索托拉西布治疗后既往免疫治疗的非小细胞肺癌患者的肝毒性:全面的临床和药代动力学分析。
EBioMedicine. 2024 Apr;102:105074. doi: 10.1016/j.ebiom.2024.105074. Epub 2024 Mar 19.
9
METhodological RadiomICs Score (METRICS): a quality scoring tool for radiomics research endorsed by EuSoMII.方法学放射组学评分(METRICS):一种由欧洲医学影像信息学会(EuSoMII)认可的放射组学研究质量评分工具。
Insights Imaging. 2024 Jan 17;15(1):8. doi: 10.1186/s13244-023-01572-w.
10
Identification of non-actionable mutations with prognostic and predictive value in patients with advanced or metastatic non-small cell lung cancer.鉴定晚期或转移性非小细胞肺癌患者具有预后和预测价值的非治疗性突变。
Clin Transl Oncol. 2024 Jun;26(6):1384-1394. doi: 10.1007/s12094-023-03362-8. Epub 2024 Jan 6.

可切除的伴有表皮生长因子受体(EGFR)突变和间变性淋巴瘤激酶(ALK)重排的非鳞状非小细胞肺癌的围手术期策略

Perioperative Strategies in Resectable Non-Squamous Non-Small Cell Lung Cancer with EGFR Mutations and ALK Rearrangement.

作者信息

Petrella Francesco, Cara Andrea, Cassina Enrico Mario, Degiovanni Sara, Libretti Lidia, Lo Torto Sara, Pirondini Emanuele, Raveglia Federico, Spinelli Francesca, Tuoro Antonio, Rizzo Stefania

机构信息

Department of Thoracic Surgery, Fondazione IRCCS San Gerardo dei Tintori, 20900 Monza, Italy.

Department of Thoracic Surgery, Tor Vergata University Polyclinic, 00133 Roma, Italy.

出版信息

Cancers (Basel). 2025 May 31;17(11):1844. doi: 10.3390/cancers17111844.

DOI:10.3390/cancers17111844
PMID:40507325
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12153872/
Abstract

Lung cancer is the leading cause of cancer-related death worldwide, ranking first among men and second among women for both incidence and mortality. Surgery remains the primary treatment for early-stage, resectable non-small cell lung cancer (NSCLC), encompassing stages I and selected cases of stage IIIB. For patients with stage II to III disease, as well as some stage IB tumors, neoadjuvant or adjuvant systemic therapies are recommended. It is well recognized that specific driver gene mutations play a critical role in tumor progression and aggressiveness, and patients with these genetic alterations may benefit from targeted treatment approaches. These alterations are referred to as "druggable", "targetable", or "actionable", representing specific targets for personalized treatments. Tyrosine kinase inhibitors (TKIs) are now the preferred first-line treatment for patients harboring mutations in EGFR, ALK, ROS1, and BRAF. Additionally, targeted therapies exist for patients with alterations in RET, ERBB2, KRAS, MET, and NTRK, either for those who have received prior treatments or as part of ongoing clinical trials. The success of targeted therapies is reshaping treatment approaches for NSCLC with targetable driver gene alterations, both in early-stage and locally advanced settings. This review focuses on current therapeutic strategies that combine targeted therapies with surgical resection in patients with resectable non-small cell lung cancer (NSCLC) harboring actionable driver gene alterations.

摘要

肺癌是全球癌症相关死亡的主要原因,在男性和女性的发病率和死亡率中均排名第一和第二。手术仍然是早期、可切除的非小细胞肺癌(NSCLC)的主要治疗方法,包括I期和部分IIIB期病例。对于II至III期疾病的患者以及一些IB期肿瘤患者,建议进行新辅助或辅助全身治疗。众所周知,特定的驱动基因突变在肿瘤进展和侵袭性中起关键作用,具有这些基因改变的患者可能从靶向治疗方法中获益。这些改变被称为“可药物治疗的”、“可靶向的”或“可采取行动的”,代表个性化治疗的特定靶点。酪氨酸激酶抑制剂(TKIs)现在是携带EGFR、ALK、ROS1和BRAF突变患者的首选一线治疗药物。此外,对于RET、ERBB2、KRAS、MET和NTRK发生改变的患者,无论是接受过先前治疗的患者还是作为正在进行的临床试验的一部分,都有靶向治疗方法。靶向治疗的成功正在重塑具有可靶向驱动基因改变的NSCLC的治疗方法,无论是在早期还是局部晚期情况下。本综述重点关注在具有可采取行动的驱动基因改变的可切除非小细胞肺癌(NSCLC)患者中,将靶向治疗与手术切除相结合的当前治疗策略。