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MET酪氨酸激酶抑制剂引起的非小细胞肺癌患者外周水肿的综合管理:一项叙述性综述

Comprehensive management of MET tyrosine kinase inhibitor-induced peripheral edema in patients with -altered non-small-cell lung cancer: a narrative review.

作者信息

Lin Jia-Xin, Sun Hao, Peng Ying-Long, Xie Zhi, Liu Si-Yang Maggie, Wu Yi-Long

机构信息

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

出版信息

Transl Lung Cancer Res. 2025 Apr 30;14(4):1482-1495. doi: 10.21037/tlcr-24-866. Epub 2025 Apr 17.


DOI:10.21037/tlcr-24-866
PMID:40386723
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12082197/
Abstract

BACKGROUND AND OBJECTIVE: The mesenchymal-epithelial transition factor (MET) proto-oncogene plays an important role in the development of non-small cell lung cancer (NSCLC). MET tyrosine kinase inhibitors (TKIs) have shown promising antitumor activity in patients with NSCLC harboring MET alterations. Peripheral edema (PE), the most common adverse event of MET TKIs, has received increasing attention from clinicians. The aim of this review is to describe the incidence, potential molecular mechanisms, diagnosis, and management of MET TKI-induced PE, to increase the recognition and standardize the management of PE. METHODS: We conducted a comprehensive literature search across PubMed, Wanfang Med Online, China National Knowledge Infrastructure (CNKI), and the oncology conferences websites for related studies published between 2000 and 2023. Of the 491 titles screened, we identified 80 research articles fitting the inclusion criteria and a comprehensive literature review was conducted. The review incorporated patient conditions, comprehensive examinations, and clinical experiences to propose a standardized management framework. KEY CONTENT AND FINDINGS: The review focused on the incidence of MET TKI-induced PE, its potential molecular mechanisms, diagnostic criteria, and management strategies. The etiology of edema is complex in cancer patients; however, it may involve treatment-related increases in vascular permeability, impacts on renal function, and hypoalbuminemia. Based on the literature review, a diagnostic and comprehensive management approach for MET TKI-induced PE is proposed, which includes prevention strategies, non-pharmacological treatments, pharmacological interventions, and dosage adjustments related to MET TKIs. CONCLUSIONS: In this review, we propose a diagnostic and comprehensive management approach for MET TKI-induced PE. By standardizing management, clinicians can enhance patient care for those treated with MET TKIs, facilitating earlier detection of PE, reducing patient suffering, and improving treatment adherence and outcomes.

摘要

背景与目的:间充质-上皮转化因子(MET)原癌基因在非小细胞肺癌(NSCLC)的发生发展中起重要作用。MET酪氨酸激酶抑制剂(TKIs)在携带MET改变的NSCLC患者中显示出有前景的抗肿瘤活性。外周水肿(PE)是MET TKIs最常见的不良事件,已受到临床医生越来越多的关注。本综述的目的是描述MET TKI诱导的PE的发生率、潜在分子机制、诊断和管理,以提高对PE的认识并规范其管理。 方法:我们在PubMed、万方医学网、中国知网和肿瘤学会议网站上进行了全面的文献检索,以查找2000年至2023年期间发表的相关研究。在筛选的491篇标题中,我们确定了80篇符合纳入标准的研究文章,并进行了全面的文献综述。该综述结合患者情况、综合检查和临床经验,提出了一个标准化的管理框架。 关键内容与发现:该综述重点关注MET TKI诱导的PE的发生率、潜在分子机制、诊断标准和管理策略。癌症患者水肿的病因复杂;然而,它可能涉及与治疗相关的血管通透性增加、对肾功能的影响和低白蛋白血症。基于文献综述,提出了一种针对MET TKI诱导的PE的诊断和综合管理方法,包括预防策略、非药物治疗、药物干预以及与MET TKIs相关的剂量调整。 结论:在本综述中,我们提出了一种针对MET TKI诱导的PE的诊断和综合管理方法。通过规范管理,临床医生可以加强对接受MET TKIs治疗患者的护理,促进PE的早期发现,减轻患者痛苦,并提高治疗依从性和治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc10/12082197/537765975ee1/tlcr-14-04-1482-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc10/12082197/24f2b3dc8c3c/tlcr-14-04-1482-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc10/12082197/537765975ee1/tlcr-14-04-1482-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc10/12082197/24f2b3dc8c3c/tlcr-14-04-1482-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc10/12082197/537765975ee1/tlcr-14-04-1482-f2.jpg

相似文献

[1]
Comprehensive management of MET tyrosine kinase inhibitor-induced peripheral edema in patients with -altered non-small-cell lung cancer: a narrative review.

Transl Lung Cancer Res. 2025-4-30

[2]
Epidermal Growth Factor Receptor Mutation (EGFR) Testing for Prediction of Response to EGFR-Targeting Tyrosine Kinase Inhibitor (TKI) Drugs in Patients with Advanced Non-Small-Cell Lung Cancer: An Evidence-Based Analysis.

Ont Health Technol Assess Ser. 2010

[3]
Safety of MET Tyrosine Kinase Inhibitors in Patients With MET Exon 14 Skipping Non-small Cell Lung Cancer: A Clinical Review.

Clin Lung Cancer. 2022-5

[4]
Real world experience with MET inhibitors in MET exon 14 skipping mutated non-small cell lung cancer: largest Indian perspective.

Discov Oncol. 2025-3-8

[5]
Mutations in the MET tyrosine kinase domain and resistance to tyrosine kinase inhibitors in non-small-cell lung cancer.

Respir Res. 2023-1-25

[6]
Anti-cancer Effects of Polyphenolic Compounds in Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor-resistant Non-small Cell Lung Cancer.

Pharmacogn Mag. 2017

[7]
MET tyrosine kinase inhibitors in combination with EGFR tyrosine kinase inhibitors in NSCLC patients with EGFR mutations and acquired MET alterations: a systematic review and meta-analysis.

BMC Cancer. 2025-4-18

[8]
A novel mesenchymal epithelial transition (MET) inhibitor, CB538, relieves acquired resistance in -mutated -amplified non-small cell lung cancer.

Transl Cancer Res. 2025-3-30

[9]
The Efficacy and Safety of Treating Acquired MET Resistance Through Combinations of Parent and MET Tyrosine Kinase Inhibitors in Patients With Metastatic Oncogene-Driven NSCLC.

JTO Clin Res Rep. 2024-1-18

[10]
Crizotinib with or without an EGFR-TKI in treating EGFR-mutant NSCLC patients with acquired MET amplification after failure of EGFR-TKI therapy: a multicenter retrospective study.

J Transl Med. 2019-2-21

本文引用的文献

[1]
Capmatinib efficacy for METex14 non-small cell lung cancer patients: Results of the IFCT-2104 CAPMATU study.

Lung Cancer. 2024-10

[2]
MET targeted therapy in non-small cell lung cancer patients with exon 14-skipping mutations.

Transl Lung Cancer Res. 2024-4-29

[3]
Tepotinib in patients with non-small cell lung cancer with high-level MET amplification detected by liquid biopsy: VISION Cohort B.

Cell Rep Med. 2023-11-21

[4]
MET in Non-Small-Cell Lung Cancer (NSCLC): Cross 'a Long and Winding Road' Looking for a Target.

Cancers (Basel). 2023-9-28

[5]
Overall Survival with Osimertinib in Resected -Mutated NSCLC.

N Engl J Med. 2023-7-13

[6]
Tepotinib Treatment in Patients With MET Exon 14-Skipping Non-Small Cell Lung Cancer: Long-term Follow-up of the VISION Phase 2 Nonrandomized Clinical Trial.

JAMA Oncol. 2023-9-1

[7]
Gumarontinib in patients with non-small-cell lung cancer harbouring exon 14 skipping mutations: a multicentre, single-arm, open-label, phase 1b/2 trial.

EClinicalMedicine. 2023-4-6

[8]
[Chinese multidisciplinary expert consensus on the management of adverse drug reactions associated with savolitinib].

Zhonghua Zhong Liu Za Zhi. 2023-4-23

[9]
Pseudo-acute kidney injury secondary to tepotinib.

Clin Kidney J. 2022-8-1

[10]
Potent antitumor activity of ensartinib in MET exon 14 skipping-mutated non-small cell lung cancer.

Cancer Lett. 2023-5-1

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