Suppr超能文献

根据表皮生长因子受体(EGFR)突变状态评估局部晚期非小细胞肺癌同步放化疗疗效。

Evaluation of concurrent chemoradiotherapy for locally advanced NSCLC according to EGFR mutation status.

作者信息

Ishihara Mikiko, Igawa Satoshi, Sasaki Jiichiro, Otani Sakiko, Fukui Tomoya, Ryuge Shinichiro, Katono Ken, Hiyoshi Yasuhiro, Kasajima Masashi, Mitsufuji Hisashi, Kubota Masaru, Yokoba Masanori, Katagiri Masato, Sekiguchi Akane, Soda Itaru, Ishiyama Hiromichi, Hayakawa Kazushige, Masuda Noriyuki

机构信息

Department of Respiratory Medicine, Kitasato University School of Medicine, Sagamihara, Kanagawa 252-0374, Japan.

Research and Development Center for New Medical Frontiers, Kitasato University School of Medicine, Sagamihara, Kanagawa 252-0374, Japan.

出版信息

Oncol Lett. 2017 Jul;14(1):885-890. doi: 10.3892/ol.2017.6231. Epub 2017 May 23.

Abstract

Concurrent chemoradiotherapy (cCRT) is the standard treatment for patients with locally advanced non-small cell lung cancer (LA-NSCLC). However, the efficacy and safety of this treatment has not been compared between patients who possess epidermal growth factor receptor (EGFR) mutations and patients with wild-type EGFR. The objective of the present study was to evaluate the effect of the presence of EGFR gene mutations in patients with LA-NSCLC receiving cCRT. Between January 2007 and December 2013, the records of 64 patients were reviewed retrospectively. The data were statistically analyzed to evaluate the efficacy of cCRT according to EGFR mutation status. In total, 15/64 were revealed to possess EGFR mutations, 23%, and comprised the mutant EGFR group. The progression-free survival time was significantly shorter in the mutant EGFR group compared with the patient group with tumors exhibiting wild-type EGFR, 6.3 and 9.5 months, respectively (P<0.001). The overall survival rate was longer in the mutant EGFR group compared with the wild-type EGFR group, although the difference was not statistically significant, 37.1 and 21.1 months, respectively (P=0.26). The disease recurred in all of the patients of the mutant EGFR group, whilst the recurrence rate in the wild-type EGFR group was 89%. The frequency of distant metastasis was significantly higher in the mutant EGFR group compared with the wild-type EGFR group. In conclusion, these data suggest that additional studies are required to identify strategies for reinforcing the efficacy of cCRT, with a focus on the potential use of EGFR tyrosine kinase inhibitors for patients exhibiting an EGFR mutation.

摘要

同步放化疗(cCRT)是局部晚期非小细胞肺癌(LA-NSCLC)患者的标准治疗方法。然而,这种治疗方法在具有表皮生长因子受体(EGFR)突变的患者和野生型EGFR患者之间的疗效和安全性尚未进行比较。本研究的目的是评估EGFR基因突变对接受cCRT的LA-NSCLC患者的影响。回顾性分析了2007年1月至2013年12月期间64例患者的记录。根据EGFR突变状态对数据进行统计分析,以评估cCRT的疗效。总共64例患者中有15例(23%)被发现具有EGFR突变,组成了突变型EGFR组。突变型EGFR组的无进展生存期明显短于肿瘤表现为野生型EGFR的患者组,分别为6.3个月和9.5个月(P<0.001)。突变型EGFR组的总生存率长于野生型EGFR组,分别为37.1个月和21.1个月,尽管差异无统计学意义(P=0.26)。突变型EGFR组的所有患者均出现疾病复发,而野生型EGFR组的复发率为89%。突变型EGFR组的远处转移频率明显高于野生型EGFR组。总之,这些数据表明需要进一步研究以确定增强cCRT疗效的策略,重点是对具有EGFR突变的患者潜在使用EGFR酪氨酸激酶抑制剂。

相似文献

引用本文的文献

本文引用的文献

5
Cancer treatment and survivorship statistics, 2012.癌症治疗与生存统计,2012 年。
CA Cancer J Clin. 2012 Jul-Aug;62(4):220-41. doi: 10.3322/caac.21149. Epub 2012 Jun 14.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验