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首页> 外文期刊>Targeted oncology >Non-Small-Cell Lung Cancer (NSCLC) Harboring ALK Translocations: Clinical Characteristics and Management in a Real-Life Setting: a French Retrospective Analysis (GFPC 02–14 Study)
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Non-Small-Cell Lung Cancer (NSCLC) Harboring ALK Translocations: Clinical Characteristics and Management in a Real-Life Setting: a French Retrospective Analysis (GFPC 02–14 Study)

机译:非小细胞肺癌(NSCLC)覆盖ALK易位:现实生活环境中的临床特点和管理:法国回顾性分析(GFPC 02-14研究)

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Abstract Background Chromosomal translocations involving the anaplastic lymphoma kinase gene ( ALK ) are rare oncogenic events found in 3–5% of non-small-cell lung cancers (NSCLC). Limited data have been published on the management of these patients outside clinical trials. Objective To investigate the clinical characteristics and management of patients with NSCLC harboring ALK translocations ( ALK +) in a real-life setting in France. Methods This multicenter, observational, retrospective study included all NSCLC patients harboring ALK translocations diagnosed in participating centers between January 2012 and December 2014. Patient data include clinical characteristics, disease management, and outcomes [progression-free survival (PFS) and overall survival (OS)]. Results The 31 participating centers reported data on 132 patients, of whom 51% ( n ?=?67) were male. The median age was 60.1 ±?14.5 (standard deviation)?years; 89% ( n ?=?106/119) had performance status 0/1 at diagnosis; 79% ( n ?=?103/130) were non- or former smokers; 93% ( n ?=?120/129) had adenocarcinomas and 74%( n ?=?97)/19%( n ?=?25)/7%( n ?=?10) had disease stages IV/III/I-II at diagnosis, respectively; co-mutations included EGFR ( n ?=?2), BRAF ( n ?=?2), KRAS ( n ?=?1), and HER2 ( n ?=?1). Of the patients with stage IV NSCLC ( n ?=?97), 96% received first-line treatment [75% chemotherapy-based, 21% ALK tyrosine kinase inhibitor (TKI)], with an associated response rate (RR), disease-control rate (DCR), and PFS of 42%, 64%, and 7.5 [95% confidence interval (CI) 5.9–9.5] months, respectively; 62% received second-line treatment (28% chemotherapy, 72% ALK TKI) with an associated RR, DCR, and PFS of 43.4%, 70%, and 4.7 (95% CI 4.0–8.1) months, respectively. The 2-year OS was 56.7% (95% CI 45.5–70.4%); median OS was not reached. Conclusion The results of this real-life analysis suggest that the prognosis of NSCLC patients with the ALK translocation may be better than that of the overall NSCLC population, but the outcomes were poorer than those of ALK + NSCLC patients included in clinical studies.
机译:摘要背景涉及包膜性淋巴瘤激酶基因(ALK)的染色体易位是罕见的致癌事件,以3-5%的非小细胞肺癌(NSCLC)。已经发表了有限的数据,这些数据在临床试验外的这些患者的管理中。目的探讨NSCLC患有ALK易位(ALK +)患者患者的临床特征和管理。方法对多中心,观测,回顾性研究包括所有NSCLC患者,涉及2012年1月至2014年1月诊断为参与中心诊断的ALK易位的患者。患者数据包括临床特征,疾病管理和结果[无进展生存(PFS)和整体存活(OS )]。结果31种参与中心报告了132名患者的数据,其中51%(n?=?67)是男性。中位年龄为60.1±14.5(标准差)?岁; 89%(n?= 106/119)在诊断时具有性能状态0/1; 79%(n?= 103/130)是非或前吸烟者; 93%(n?= 120/129)具有腺癌和74%(n?= 97)/ 19%(n?= 25)/ 7%(n?=?10)疾病阶段IV / III / I-II分别诊断;共突变包括EGFR(n?=Δ2),BRAF(n?=?2),KRAS(n?=?1)和HER2(n?=?1)。患有阶段IV NMSCLC(N?= 97)的患者,96%接受初系治疗[75%的化疗,21%ALK酪氨酸激酶抑制剂(TKI)],具有相关的反应率(RR),疾病-Control速率(DCR)和PFS分别为42%,64%和7.5 [95%置信区间(CI)5.9-9.5]月份; 62%接受二线治疗(28%化疗,72%ALK TKI),相关的RR,DCR和PFS分别为43.4%,70%和4.7(95%CI 4.0-8.1)个月。 2年的OS是56.7%(95%CI 45.5-70.4%);没有达到中位的操作系统。结论这种现实生活分析的结果表明,NSCLC患者的ALAK易位的预后可能比整体NSCLC群体更好,但结果比临床研究所含的ALK + NSCLC患者差。

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