Sarcopenia is a predictive marker for response to erlotinib in patients with lung adenocancer

IF 0.1
H. Çınkır, T. Kus, G. Aktas, U. Elboğa
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引用次数: 1

Abstract

Background: Adenocancer pathologic subtype, smoking history, and women gender have been known to predict the parameters such as the sensitivity to epidermal growth factor receptor tyrosine kinase inhibitors in advanced non-small cell lung cancer (NSCLC); however, we need new predictive markers as well as driver mutations for better treatment options. The aim of this study is to investigate the predictive role of sarcopenia in lung adenocancer patients treated with erlotinib. Materials and Methods: This study was designed as retrospectively. Skeletal muscle index (SMI) was measured with a single cross-sectional area of the muscle at the third lumber vertebra (L3, cm2)/(height × height)(m2). Sarcopenia was defined by median cutoff values of SMI of women (<28.2 cm2/m2) and men (<32.7 cm2/m2). The predictive role of sarcopenia and other parameters was assessed by the cox-regression model. Results: The median age was 56 years (range, 36–84). Median progression-free survival (PFS) was 38 (95% confidence interval [CI]: 21.3–54.6) weeks in the sarcopenic group and 49 (95% CI: 0–101.4) weeks in the nonsarcopenic group (P = 0.053). In multivariate analysis, the presence of sarcopenia and number of metastatis were the independent predictive factors for PFS. Disease control rate and overall survival were not significantly different between sarcopenic and nonsarcopenic groups. Conclusion: We found that the presence of sarcopenia and number of metastasis were a predictive marker in NSCLC patients treated with erlotinib. It is important to recognize sarcopenia early and manage patients accordingly.
Sarcopenia是肺腺癌患者对埃洛替尼反应的预测标志物
背景:已知腺癌的病理亚型、吸烟史和女性可预测晚期癌症(NSCLC)对表皮生长因子受体酪氨酸激酶抑制剂的敏感性等参数;然而,我们需要新的预测标志物以及驱动突变来获得更好的治疗选择。本研究的目的是研究肌肉减少症在接受埃洛替尼治疗的肺腺癌患者中的预测作用。材料与方法:本研究为回顾性设计。骨骼肌指数(SMI)是用第三腰椎处肌肉的单个横截面积(L3,cm2)/(高度×高度)(m2)测量的。Sarcopenia由女性(<28.2 cm2/m2)和男性(<32.7 cm2/m2。通过cox回归模型评估少肌症和其他参数的预测作用。结果:中位年龄为56岁(36~84岁)。少肌症组的中位无进展生存期(PFS)为38周(95%置信区间[CI]:21.3–54.6),非少肌症患者为49周(95%CI:0–101.4)(P=0.053)。在多变量分析中,少肌症的存在和转移数量是PFS的独立预测因素。肌肉减少组和非肌肉减少组的疾病控制率和总生存率没有显著差异。结论:我们发现,在接受埃洛替尼治疗的NSCLC患者中,少肌症的存在和转移数量是一个预测指标。早期识别少肌症并对患者进行相应的管理是很重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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