Abstract

PurposeIncreasing lung cancer incidence in China with a high death rate due to late diagnosis highlights the need for biomarkers, such as panels of autoantibodies (AAbs), for prediction and early lung cancer diagnosis. We conducted a study to further evaluate the clinical performance of an AAb diagnostic kit.MethodsUsing enzyme-linked immunosorbent assay, levels of seven AAbs in serum samples from 121 patients with newly diagnosed lung cancer, 84 controls (34 healthy individuals and 50 patients with benign lung disease), and 100 indeterminate solid nodules, were measured. Participants were followed up until 6 months after a positive test result to confirm lung cancer diagnosis.ResultsThe seven AAb concentration was significantly higher in lung cancer patients than in controls (P < 0.05). The seven AAb sensitivity and specificity for newly diagnosed lung cancer were 45.5% and 85.3%, respectively, while the seven AAb combined area under the curve (in lung cancer patients versus controls) was 0.660. Of the 28 patients with solid nodules with positive test results, 8 and 3 were diagnosed with lung cancer and benign lung disease, respectively, during follow-up. The positive predictive value of the experiment was 72.7%.ConclusionPositive AAb test results were associated with a high risk of lung cancer. The seven-AAb panel also had a high predictive value for detecting lung cancer in patients with solid nodules. Our seven lung cancer autoantibody types can provide an important early warning sign in the clinical setting.

Highlights

  • Lung cancer has the highest mortality rate among all common cancer types, and it has shown a trend of increasing incidence worldwide (She et al 2013)

  • We measured the levels of the seven AAbs using enzymelinked immunosorbent assay (ELISA)-based test kit purchased from Hangzhou Cancer Probe Biological Technology Co., Ltd., Room 501–505, 5th Floor, Building D, Building 688, Bin Anlu, Changhe Street, Binjiang District, Hangzhou, China

  • Our study showed that the combined AAb panel (p53, GAGE7, PGP9.5, CAGE, MAGEA1, SOX2, and GBU4-5) could differentiate patients with lung cancer from healthy controls and patients with benign lung disease

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Summary

Introduction

Lung cancer has the highest mortality rate among all common cancer types, and it has shown a trend of increasing incidence worldwide (She et al 2013). According to statistics from the American Cancer Association, there were 226,160 patients with newly diagnosed lung cancer in 2012, while 160,340 people died from lung cancer in 2012 (Siegel et al 2012). In China, 4.292 million people were diagnosed with lung cancer, and there were 2.814 million deaths due to lung cancer in 2015 (Chen et al 2016). Detection is the key to long-term survival, as the 5-year survival rate. The low sensitivity or specificity of these techniques has contributed to their ineffectiveness in detecting lung cancer at an early stage (Jemal et al 2004). Autoantibodies (AAbs) have been explored as promising biomarkers to detect lung cancer at an early stage (Ren et al 2017).

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