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Modeling the Cost-Effectiveness of Adjuvant Osimertinib for Patients with Resected EGFR-mutant Non-Small Cell Lung Cancer.奥希替尼辅助治疗切除的 EGFR 突变型非小细胞肺癌的成本效果建模。
Oncologist. 2022 May 6;27(5):407-413. doi: 10.1093/oncolo/oyac021.
2
Efficacy of adjuvant EGFR inhibitors and impact of clinical factors in resected -mutated non-small-cell lung cancer: a meta-analysis.辅助性表皮生长因子受体抑制剂的疗效及临床因素对切除的表皮生长因子受体突变型非小细胞肺癌的影响:一项荟萃分析
Future Oncol. 2022 Mar;18(9):1159-1169. doi: 10.2217/fon-2021-0934. Epub 2022 Feb 3.
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Health-Related Quality of Life Outcomes in Patients with Resected Epidermal Growth Factor Receptor-Mutated Non-Small Cell Lung Cancer Who Received Adjuvant Osimertinib in the Phase III ADAURA Trial.III 期 ADAURA 试验中接受辅助奥希替尼治疗的表皮生长因子受体突变型非小细胞肺癌患者的健康相关生活质量结局。
Clin Cancer Res. 2022 Jun 1;28(11):2286-2296. doi: 10.1158/1078-0432.CCR-21-3530.
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Genomic signatures define three subtypes of EGFR-mutant stage II-III non-small-cell lung cancer with distinct adjuvant therapy outcomes.基因组特征定义了三种不同辅助治疗结果的 EGFR 突变型 II-III 期非小细胞肺癌亚型。
Nat Commun. 2021 Nov 8;12(1):6450. doi: 10.1038/s41467-021-26806-7.
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Randomized Phase III Study of Gefitinib Versus Cisplatin Plus Vinorelbine for Patients With Resected Stage II-IIIA Non-Small-Cell Lung Cancer With Mutation (IMPACT).吉非替尼对比顺铂联合长春瑞滨用于可切除的II-IIIA期非小细胞肺癌伴突变患者的随机III期研究(IMPACT)
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The Reality of Lung Cancer Paradox: The Impact of Body Mass Index on Long-Term Survival of Resected Lung Cancer. A French Nationwide Analysis from the Epithor Database.肺癌悖论的现实:体重指数对切除肺癌患者长期生存的影响。来自Epithor数据库的法国全国性分析。
Cancers (Basel). 2021 Sep 12;13(18):4574. doi: 10.3390/cancers13184574.
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Efficacy and Safety of Neoadjuvant Targeted Therapy vs. Neoadjuvant Chemotherapy for Stage IIIA EGFR-Mutant Non-small Cell Lung Cancer: A Systematic Review and Meta-Analysis.新辅助靶向治疗与新辅助化疗治疗ⅢA期表皮生长因子受体(EGFR)突变型非小细胞肺癌的疗效与安全性:一项系统评价和Meta分析
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FDA Approval Summary: Osimertinib for Adjuvant Treatment of Surgically Resected Non-Small Cell Lung Cancer, a Collaborative Project Orbis Review.FDA 批准概要:奥希替尼用于手术切除的非小细胞肺癌的辅助治疗,Orbis 审查合作项目。
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Icotinib versus chemotherapy as adjuvant treatment for stage II-IIIA EGFR-mutant non-small-cell lung cancer (EVIDENCE): a randomised, open-label, phase 3 trial.厄洛替尼对比化疗用于 EGFR 突变型 II-IIIA 期非小细胞肺癌辅助治疗(EVIDENCE):一项随机、开放标签、III 期临床试验。
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手术期突变型非小细胞肺癌:酪氨酸激酶抑制剂的地位如何?

-Mutant Non-Small-Cell Lung Cancer at Surgical Stages: What Is the Place for Tyrosine Kinase Inhibitors?

作者信息

Cansouline Xavier, Lipan Béatrice, Sizaret Damien, Tallet Anne, Vandier Christophe, Carmier Delphine, Legras Antoine

机构信息

Department of Thoracic Surgery, Tours University Hospital, 37170 Chambray-Lès-Tours, France.

Nutrition, Croissance et Cancer, INSERM UMR 1069, University of Tours, 37000 Tours, France.

出版信息

Cancers (Basel). 2022 Apr 30;14(9):2257. doi: 10.3390/cancers14092257.

DOI:10.3390/cancers14092257
PMID:35565386
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9099844/
Abstract

The ADAURA trial has been significant for the perception of tyrosine kinase inhibitors (TKIs) as a tool for early stage non-small-cell lung cancer (NSCLC). It produced such great insight that the main TKI, Osimertinib, was rapidly integrated into international guidelines for adjuvant use. However, -mutant NSCLC is a complex entity and has various targeting drugs, and the benefits for patients might not be as clear as they seem. We reviewed trials and meta-analyses considering TKI adjuvant and neoadjuvant use. We also explored the influence of mutation variability and financial evaluations. We found that TKIs often show disease-free survival (DFS) benefits, yet studies have struggled to improve the overall survival (OS); however, the results from the literature might be confusing because of variability in the stages and mutations. The safety profiles and adverse events are acceptable, but costs remain high and accessibility might not be optimal. TKIs are promising drugs that could allow for tailored treatment designs.

摘要

ADAURA试验对于将酪氨酸激酶抑制剂(TKIs)视为早期非小细胞肺癌(NSCLC)治疗工具的认知具有重要意义。它带来了深刻见解,以至于主要的TKI药物奥希替尼迅速被纳入国际辅助治疗指南。然而,-突变型NSCLC是一个复杂的实体,有多种靶向药物,对患者的益处可能并不像看起来那么明确。我们回顾了考虑TKI辅助和新辅助使用的试验及荟萃分析。我们还探讨了突变变异性和财务评估的影响。我们发现TKIs通常显示出无病生存期(DFS)益处,但研究在改善总生存期(OS)方面仍面临困难;然而,由于分期和突变的变异性,文献结果可能令人困惑。安全性和不良事件是可接受的,但成本仍然很高,可及性可能也不理想。TKIs是有前景的药物,有望实现个性化治疗设计。