{"title":"Clinical Efficacy of Osimertinib in Patients with Advanced Non-Small Cell Lung Cancer and Its Effect on Serum CEA and VEGF Expression.","authors":"Huanyuan Wang, Xiangwu Zhou, Zhaozhen Wang, Tianzhu Lu, Baoliang Li, Sicong Jiang","doi":"10.1155/2022/3032087","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To assess the clinical efficacy of osimertinib in patients with advanced non-small cell lung cancer and its effect on serum carcinoembryonic antigen (CEA) and vascular endothelial growth factor (VEGF) expression.</p><p><strong>Methods: </strong>Between July 2018 and January 2020, 80 patients with advanced non-small cell lung cancer were assessed for eligibility and recruited. The patients were assigned at a ratio of 1 : 1 to receive either the PC regimen (pemetrexed + cisplatin) (conventional group) or osimertinib (experimental group). The primary endpoint was the clinical efficacy, and the secondary endpoints were the adverse events, expression of serum CEA and VEGF, and 2-year survival.</p><p><strong>Results: </strong>Osimertinib was associated with a significantly higher response rate and disease control rate versus pemetrexed plus cisplatin (<i>P</i> < 0.05). Osimertinib resulted in a significantly lower incidence of adverse events versus the PC regimen (<i>P</i> < 0.05). Patients given osimertinib had significantly lower levels of CEA and VEGF versus those given pemetrexed plus cisplatin (<i>P</i> < 0.05). Osimertinib was associated with a significantly higher 1-year and 2-year survival rate versus pemetrexed plus cisplatin.</p><p><strong>Conclusion: </strong>Osimertinib could inhibit the expression of serum CEA and VEGF in patients with advanced non-small cell lung cancer and reduce the adverse events with significant efficacy, so it is worthy of clinical promotion and application.</p>","PeriodicalId":8280,"journal":{"name":"Archives of Mechanics","volume":"70 1","pages":"3032087"},"PeriodicalIF":1.1000,"publicationDate":"2022-05-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9159882/pdf/","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of Mechanics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1155/2022/3032087","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"MATERIALS SCIENCE, CHARACTERIZATION & TESTING","Score":null,"Total":0}
引用次数: 1
Abstract
Objective: To assess the clinical efficacy of osimertinib in patients with advanced non-small cell lung cancer and its effect on serum carcinoembryonic antigen (CEA) and vascular endothelial growth factor (VEGF) expression.
Methods: Between July 2018 and January 2020, 80 patients with advanced non-small cell lung cancer were assessed for eligibility and recruited. The patients were assigned at a ratio of 1 : 1 to receive either the PC regimen (pemetrexed + cisplatin) (conventional group) or osimertinib (experimental group). The primary endpoint was the clinical efficacy, and the secondary endpoints were the adverse events, expression of serum CEA and VEGF, and 2-year survival.
Results: Osimertinib was associated with a significantly higher response rate and disease control rate versus pemetrexed plus cisplatin (P < 0.05). Osimertinib resulted in a significantly lower incidence of adverse events versus the PC regimen (P < 0.05). Patients given osimertinib had significantly lower levels of CEA and VEGF versus those given pemetrexed plus cisplatin (P < 0.05). Osimertinib was associated with a significantly higher 1-year and 2-year survival rate versus pemetrexed plus cisplatin.
Conclusion: Osimertinib could inhibit the expression of serum CEA and VEGF in patients with advanced non-small cell lung cancer and reduce the adverse events with significant efficacy, so it is worthy of clinical promotion and application.
期刊介绍:
Archives of Mechanics provides a forum for original research on mechanics of solids, fluids and discrete systems, including the development of mathematical methods for solving mechanical problems. The journal encompasses all aspects of the field, with the emphasis placed on:
-mechanics of materials: elasticity, plasticity, time-dependent phenomena, phase transformation, damage, fracture; physical and experimental foundations, micromechanics, thermodynamics, instabilities;
-methods and problems in continuum mechanics: general theory and novel applications, thermomechanics, structural analysis, porous media, contact problems;
-dynamics of material systems;
-fluid flows and interactions with solids.
Papers published in the Archives should contain original contributions dealing with theoretical, experimental, or numerical aspects of mechanical problems listed above.
The journal publishes also current announcements and information about important scientific events of possible interest to its readers, like conferences, congresses, symposia, work-shops, courses, etc.
Occasionally, special issues of the journal may be devoted to publication of all or selected papers presented at international conferences or other scientific meetings. However, all papers intended for such an issue are subjected to the usual reviewing and acceptance procedure.