首页> 美国卫生研究院文献>Journal of Cancer >Impact of Weight Loss at Presentation on Survival in Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors (EGFR-TKI) Sensitive Mutant Advanced Non-small Cell Lung Cancer (NSCLC) Treated with First-line EGFR-TKI
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Impact of Weight Loss at Presentation on Survival in Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors (EGFR-TKI) Sensitive Mutant Advanced Non-small Cell Lung Cancer (NSCLC) Treated with First-line EGFR-TKI

机译:一线用EGFR-TKI治疗的体重减轻对表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)敏感突变晚期非小细胞肺癌(NSCLC)存活率的影响

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摘要

>Purpose The aim of this study is to evaluate the impact of weight loss at presentation on treatment outcomes of first-line EGFR-tyrosine kinase inhibitors (EGFR-TKI) in EGFR-TKI sensitive mutant NSCLC patients.>Methods We retrospectively analyzed the clinical outcomes of 75 consecutive advanced NSCLC patients with EGFR-TKI sensitive mutations (exon 19 deletion or exon 21 L858R) received first-line gefitinib or erlotinib therapy according to weight loss status at presentation in our single center.>Results Of 75 EGFR-TKI sensitive mutant NSCLC patients, 49 (65.3%) patients had no weight loss and 26 (34.7%) had weight loss at presentation, the objective response rate (ORR) to EGFR-TKI treatment were similar between the two groups (79.6% vs. 76.9%, p = 0.533). Patients without weight loss at presentation had significantly longer median progression free survival (PFS) (12.4 months vs. 7.6 months; hazard ratio [HR] 0.356, 95% confidence interval [CI] 0.212-0.596, p < 0.001) and overall survival (OS) (28.5 months vs. 20.7 months; HR 0.408, 95% CI 0.215-0.776, p = 0.006) than those with weight loss at presentation; moreover, the stratified analysis by EGFR-TKI sensitive mutation types also found similar trend between these two groups except for OS in EGFR exon 21 L858R mutation patients. Multivariate analysis identified weight loss at presentation and EGFR-TKI sensitive mutation types were independent predictive factors for PFS and OS.>Conclusions Weight loss at presentation had a detrimental impact on PFS and OS in EGFR-TKI sensitive mutant advanced NSCLC patients treated with first-line EGFR-TKI. It should be considered as an important factor in the treatment decision or designing of EGFR-TKI clinical trials.
机译:>目的这项研究的目的是评估就诊时体重减轻对EGFR-TKI敏感突变型NSCLC患者一线EGFR-酪氨酸激酶抑制剂(EGFR-TKI)的治疗效果的影响。 strong>方法我们回顾性分析了75例连续的晚期EGFR-TKI敏感突变(外显子19缺失或外显子21 L858R)接受治疗的晚期NSCLC患者的临床状况,这些患者均根据吉美替尼或厄洛替尼一线治疗的体重减轻情况进行了分析。 >结果在75例EGFR-TKI敏感的突变型NSCLC患者中,有49例(65.3%)的患者无体重减轻,有26例(34.7%)的患者在就诊时体重下降,客观缓解率(ORR)两组之间的EGFR-TKI治疗相似)(79.6%vs. 76.9%,p = 0.533)。就诊时没有体重减轻的患者中位无进展生存期(PFS)明显更长(12.4个月vs. 7.6个月;危险比[HR] 0.356,95%置信区间[CI] 0.212-0.596,p <0.001)和总生存期( OS)(28.5个月vs. 20.7个月; HR 0.408,95%CI 0.215-0.776,p = 0.006)此外,对EGFR-TKI敏感突变类型的分层分析还发现,除了EGFR外显子21 L858R突变患者的OS以外,这两组之间的趋势相似。多变量分析确定呈现时体重减轻,而EGFR-TKI敏感突变类型是PFS和OS的独立预测因素。>结论呈现时体重下降对晚期EGFR-TKI敏感突变体的PFS和OS有不利影响一线EGFR-TKI治疗的NSCLC患者。在EGFR-TKI临床试验的治疗决策或设计中,应将其视为重要因素。

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