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本文引用的文献

1
EGFR Mutation Impact on Definitive Concurrent Chemoradiation Therapy for Inoperable Stage III Adenocarcinoma.III 期不可手术肺腺癌根治性同步放化疗中 EGFR 突变的影响。
J Thorac Oncol. 2015 Dec;10(12):1720-5. doi: 10.1097/JTO.0000000000000675.
2
Epidermal growth factor receptor mutation is associated with longer local control after definitive chemoradiotherapy in patients with stage III nonsquamous non-small-cell lung cancer.表皮生长因子受体突变与Ⅲ期非鳞状非小细胞肺癌患者根治性放化疗后更长的局部控制时间相关。
Int J Radiat Oncol Biol Phys. 2015 Jan 1;91(1):140-8. doi: 10.1016/j.ijrobp.2014.08.344. Epub 2014 Oct 13.
3
The impact of clinical outcomes according to EGFR mutation status in patients with locally advanced lung adenocarcinoma who recieved concurrent chemoradiotherapy.接受同步放化疗的局部晚期肺腺癌患者中,根据表皮生长因子受体(EGFR)突变状态对临床结局的影响。
Am J Clin Oncol. 2014 Apr;37(2):144-7. doi: 10.1097/COC.0b013e31826e04f9.
4
Clinical outcomes of thoracic radiotherapy for locally advanced NSCLC with EGFR mutations or EML4-ALK rearrangement.局部晚期 NSCLC 有 EGFR 突变或 EML4-ALK 重排患者接受胸部放疗的临床结局。
Anticancer Res. 2012 Oct;32(10):4533-7.
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.
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Erlotinib versus standard chemotherapy as first-line treatment for European patients with advanced EGFR mutation-positive non-small-cell lung cancer (EURTAC): a multicentre, open-label, randomised phase 3 trial.厄洛替尼对比标准化疗用于治疗欧洲晚期 EGFR 突变阳性非小细胞肺癌患者的一线治疗(EURTAC):一项多中心、开放标签、随机、3 期临床试验。
Lancet Oncol. 2012 Mar;13(3):239-46. doi: 10.1016/S1470-2045(11)70393-X. Epub 2012 Jan 26.
7
Targeted agents in non-small cell lung cancer (NSCLC): clinical developments and rationale for the combination with thoracic radiotherapy.非小细胞肺癌(NSCLC)的靶向药物:临床进展及与胸部放疗联合的原理。
Cancer Treat Rev. 2012 Oct;38(6):626-40. doi: 10.1016/j.ctrv.2011.11.003. Epub 2011 Dec 22.
8
Erlotinib versus chemotherapy as first-line treatment for patients with advanced EGFR mutation-positive non-small-cell lung cancer (OPTIMAL, CTONG-0802): a multicentre, open-label, randomised, phase 3 study.厄洛替尼对比化疗用于治疗晚期 EGFR 突变阳性非小细胞肺癌患者的一线治疗(OPTIMAL、CTONG-0802):一项多中心、开放标签、随机、III 期研究。
Lancet Oncol. 2011 Aug;12(8):735-42. doi: 10.1016/S1470-2045(11)70184-X. Epub 2011 Jul 23.
9
Single-agent gefitinib with concurrent radiotherapy for locally advanced non-small cell lung cancer harboring mutations of the epidermal growth factor receptor.表皮生长因子受体突变的局部晚期非小细胞肺癌患者采用单药吉非替尼同步放疗。
Lung Cancer. 2011 May;72(2):199-204. doi: 10.1016/j.lungcan.2010.08.016. Epub 2010 Sep 9.
10
Chemoradiotherapy and gefitinib in stage III non-small cell lung cancer with epidermal growth factor receptor and KRAS mutation analysis: cancer and leukemia group B (CALEB) 30106, a CALGB-stratified phase II trial.表皮生长因子受体和 KRAS 突变分析指导下的 III 期非小细胞肺癌的放化疗联合吉非替尼治疗:癌症和白血病组 B(CALEB)30106,一项 CALGB 分层的 II 期试验。
J Thorac Oncol. 2010 Sep;5(9):1382-90. doi: 10.1097/JTO.0b013e3181eba657.

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.

DOI:10.3892/ol.2017.6231
PMID:28693247
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5494758/
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。