Serum albumin is a strong predictor of survival in patients with advanced-stage non-small cell lung cancer treated with erlotinib

被引:58
作者
Fiala, O. [1 ,2 ,3 ]
Pesek, M. [2 ,4 ]
Finek, J. [1 ,2 ]
Racek, J. [2 ,5 ]
Minarik, M. [6 ,7 ]
Benesova, L. [6 ]
Bortlicek, Z. [8 ]
Sorejs, O. [1 ,2 ]
Kucera, R. [2 ,9 ]
Topolcan, O. [2 ,9 ]
机构
[1] Charles Univ Prague, Sch Med, Dept Radiotherapy & Oncol, Prague, Czech Republic
[2] Charles Univ Prague, Teaching Hosp Pilsen, Prague, Czech Republic
[3] Charles Univ Prague, Fac Med Pilsen, Biomed Ctr, Prague, Czech Republic
[4] Charles Univ Prague, Sch Med, Dept Pneumol, Prague, Czech Republic
[5] Charles Univ Prague, Sch Med, Ist Clin Biochem & Hematol, Prague, Czech Republic
[6] Genomac Res Inst, Ctr Appl Genom Solid Tumors, Prague, Czech Republic
[7] Charles Univ Prague, Fac Sci, Dept Analyt Chem, Prague, Czech Republic
[8] Masaryk Univ, Fac Med, Inst Biostat & Anal, Brno, Czech Republic
[9] Charles Univ Prague, Sch Med, Dept Nucl Med, Prague, Czech Republic
关键词
albumin; lung cancer; NSCLC; EGFR-TKI; erlotinib; prediction; biomarker; NUTRITIONAL-STATUS; OPEN-LABEL; 1ST-LINE TREATMENT; CHEMOTHERAPY; EGFR; MULTICENTER; GEFITINIB; MALNUTRITION; INFLAMMATION; MUTATIONS;
D O I
10.4149/318_151001N512
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Molecular targeted therapy based on tyrosine kinase inhibitors (TKI), directed at epidermal growth factor receptor (EGFR) is one of the novel effective agents in management of advanced-stage of Non Small Cell Lung cancer (NSCLC). However several candidate predictors have been extensively studied, apart from activating EGFR gene mutations, no reliable biochemical or molecular predictors of response to erlotinib have been validated. The aim of our retrospective study was to evaluate the association of baseline serum albumin with outcomes in a large cohort of patients with advanced-stage NSCLC treated with erlotinib. Clinical data of 457 patients with locally-advanced (III B) or metastatic stage (IV) NSCLC treated with erlotinib were analysed. Serum samples were collected and the measurement was performed one day before the initiation of erlotinib treatment. Before the treatment initiation, low albumin was (<35 g/l) measured in 37 (8.1%) patients and normal albumin (>= 35 g/l) was measured in 420 (91.9%). The median PFS and OS for patients with low serum albumin was 0.9 and 1.9 months compared to 1.9 and 11.4 months for patients with normal serum albumin (p=0.001 and p<0.001). The multivariate Cox proportional hazards model revealed that EGFR mutation status (HR=2.50; CI: 1.59-3.92; p<0.001) and pretreatment serum albumin (HR=1.73; CI: 1.21-2.47; p=0.003) were significant independent predictive factors for PFS, whereas EGFR mutation status (HR=3.14; CI: 1.70-5.81; p<0.001), stage (HR=1.48; CI: 1.09-2.02; p=0.013), ECOG PS (HR=1.77; CI: 1.37-2.29; p<0.001) and pretreatment serum albumin (HR=4.60; CI: 2.98-7.10;p<0.001) were significant independent predictive factors for OS. In conclusion, the results of present retrospective study indicate that pretreatment hypoalbuminemia is associated with poor outcome of NSCLC patients treated with erlotinib. Based on these results, measuement of serum albumin is an objective laboratory method feasible for estimation of prognosis of patients with advanced-stage NSCLC.
引用
收藏
页码:471 / 476
页数:6
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