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首页> 外文期刊>Thoracic cancer. >Outcome of active anti‐cancer treatment in elderly patients with advanced non‐small cell lung cancer: A single center experience
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Outcome of active anti‐cancer treatment in elderly patients with advanced non‐small cell lung cancer: A single center experience

机译:老年晚期非小细胞肺癌患者积极抗癌治疗的结果:单中心经验

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AbstractBackgroundThis study aimed to evaluate the characteristics of active anti-cancer treatment (AAT) compared with best supportive care (BSC) in elderly patients with advanced non-small cell lung cancer (NSCLC).MethodsA retrospective analysis of 144 patients, aged 70 or older, with stage IIIb/IV NSCLC from 672 patients with confirmed lung cancer, was conducted.ResultsMedian age at diagnosis was 77 years and median survival time was five months. On multivariate analysis, AAT independently contributed to a decreased hazard ratio of death (P = 0.04), whereas male gender (P = 0.004), a body mass index of less than 18.5 (P = 0.004), and a poor performance score were associated with an increased risk of death (P 0.001). The 52 subjects receiving AAT experienced longer survival than the 92 subjects receiving BSC (median seven months [AAT] versus three months [BSC]; P 0.001). When sub-classified into five-year age intervals, AAT was a significant advantage in overall survival (OS) to patients aged 70–74, but not to those ≥75 years old.ConclusionsAAT for patients ≥70 years old with advanced NSCLC extended OS. However, care should be taken in decisions on active anti-cancer treatments for patients over 75 years old. A prospective multicenter trial is required in the near future.
机译:摘要背景:本研究旨在评估老年晚期非小细胞肺癌(NSCLC)患者的积极抗癌治疗(AAT)与最佳支持治疗(BSC)的特征。方法回顾性分析144例70岁以上的患者对672例确诊为肺癌的患者进行IIIb / IV期NSCLC治疗。结果诊断时的中位年龄为77岁,中位生存时间为5个月。在多变量分析中,AAT独立地导致死亡的危险比降低(P = 0.04),而男性(P = 0.004),体重指数小于18.5(P = 0.004)和较差的表现相关。死亡风险增加(P <0.001)。与接受BSC的92名受试者相比,接受AAT的52名受试者的生存期更长(中位7个月[AAT]对比3个月[BSC]; P <0.001)。将AAT分类为5岁年龄段时,对于70-74岁的患者,AAT在总体生存(OS)方面具有显着优势,但对于≥75岁的患者则无此优势。结论对于≥70岁的晚期NSCLC晚期OS患者,AAT 。但是,对于75岁以上的患者,在决定积极抗癌治疗时应格外小心。在不久的将来需要进行前瞻性的多中心试验。

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