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首页> 外文期刊>Journal of Cancer >First-line continual EGFR-TKI plus local ablative therapy demonstrated survival benefit in EGFR-mutant NSCLC patients with oligoprogressive disease
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First-line continual EGFR-TKI plus local ablative therapy demonstrated survival benefit in EGFR-mutant NSCLC patients with oligoprogressive disease

机译:一线持续性EGFR-TKI联合局部消融治疗证明了EGFR突变的NSCLC少进展性疾病患者的生存获益

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Introduction: The effect of local ablative therapy (LAT) for oligoprogressive epidermal growth factor receptor (EGFR) mutation non-small cell lung cancer (NSCLC) remains undetermined. This study aimed to investigate the survival benefit of addition of LAT to EGFR-TKIs in EGFR-mutant NSCLC patients with oligoprogression during TKI therapy. Materials and Methods: Patients with stage IIIB/IV EGFR mutant NSCLC who had oligoprogressive disease during the first-line EGFR-TKI therapy from March 2011 to February 2016 were identified. The primary research point were progression-free survival1 (PFS1), defined as time of initiation of TKI therapy to Response Evaluation Criteria in Solid Tumours (RECIST) 1.1 defined progress disease (PD) or death and PFS2, defined as time of initiation of TKI therapy to off-TKI PD. The second research piont inclued overal survival (OS) and safety. Results: A total of 206 patients were included. The median follow-up time was 42 months (20.0-69.6 months). The median PFS1, median PFS2 and median OS for the related cohort were 10.7 months (95% CI, 10.1-13.3 months), 18.3 months (95% CI, 17.4-19.2 months) and 37.4 months (95% CI, 35.9-38.9 months) respectively. Survival rates of 1 year, 2 years and 3 years were 94.1%, 78.9%, and 54.7%, respectively. Multivariate analysis revealed that female, EGFR exon 19 mutation, one metastatic lesion, partial or complete response to prior EGFR TKIs therapy were the independent prognostic factors. No unexpected toxicities were observed. Conclusion: The current study suggested that the addition of LAT to EGFR-TKI could provide satisfactory survival benefit for EGFR-mutant NSCLC patients with oligoprogression during first-line EGFR-TKI treatment. This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
机译:简介:局部消融治疗(LAT)对少进展性表皮生长因子受体(EGFR)突变非小细胞肺癌(NSCLC)的作用尚未确定。这项研究旨在研究在EGFR突变的NSCLC患者中,在TKI治疗期间出现寡聚进展的情况下,向EGFR-TKIs中添加LAT的生存益处。资料和方法:确定2011年3月至2016年2月在一线EGFR-TKI治疗期间发生低进展性疾病的IIIB / IV期EGFR突变NSCLC患者。主要研究点是无进展生存期1(PFS1),定义为根据实体瘤反应评估标准(RECIST)开始TKI治疗的时间1.1定义为疾病进展(PD)或死亡和PFS2,定义为开始TKI的时间非TKI PD治疗。第二项研究包括总体生存(OS)和安全性。结果:共纳入206例患者。中位随访时间为42个月(20.0-69.6个月)。相关队列的中位PFS1,中位PFS2和OS中位数分别为10.7个月(95%CI,10.1-13.3个月),18.3个月(95%CI,17.4-19.2个月)和37.4个月(95%CI,35.9-38.9)个月)。 1年,2年和3年的生存率分别为94.1%,78.9%和54.7%。多因素分析显示,女性EGFR外显子19突变,一种转移灶,对既往EGFR TKIs治疗的部分或完全反应是独立的预后因素。没有观察到意外的毒性。结论:目前的研究表明,在EGFR-TKI一线治疗期间,在EGFR-TKI中添加LAT可以为EGFR突变型NSCLC伴有低进展的NSCLC患者提供令人满意的生存获益。这是根据知识共享署名(CC BY-NC)许可(https://creativecommons.org/licenses/by-nc/4.0/)的条款分发的开放获取文章。有关完整的条款和条件,请参见http://ivyspring.com/terms。

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