TY - JOUR
T1 - Early detection of lung cancer by using an autoantibody panel in Chinese population
AU - Ren, Shengxiang
AU - Zhang, Shucai
AU - Jiang, Tao
AU - He, Yayi
AU - Ma, Zhiyong
AU - Cai, Hourong
AU - Xu, Xiaohong
AU - Li, Yan
AU - Cai, Weijing
AU - Zhou, Jing
AU - Liu, Xiaopeng
AU - Hu, Xuejun
AU - Zhang, Jun
AU - Yu, Hui
AU - Zhou, Caicun
AU - Hirsch, Fred R.
N1 - Publisher Copyright:
© 2018 Taylor & Francis Group, LLC.
PY - 2018/2/1
Y1 - 2018/2/1
N2 - We have previously identified a panel of autoantibodies (AABs), including p53, GAGE7, PGP9.5, CAGE, MAGEA1, SOX2 and GBU4-5, that was helpful in the early diagnosis of lung cancer. This large-scale, multicenter study was undertaken to validate the clinical value of this 7-AABs panel for early detection of lung cancer in a Chinese population. Two independent sets of plasma samples from 2308 participants were available for the assay of AABs (training set = 300; validation set = 2008). The concentrations of AABs were quantitated by enzyme-linked immunosorbent assay (ELISA), and the optimal cutoff value for each AAB was determined in the training set and then applied in the validation set. The value of the 7-AABs panel for the early detection of lung cancer was assessed in 540 patients who presented with ground-glass nodules (GGNs) and/or solid nodules. In the validation set, the sensitivity and specificity of the 7-AABs panel were 61% and 90%, respectively. For stage I and stage II non-small cell lung cancer (NSCLC), the sensitivity of the 7-AABs panel was 62% and 59%, respectively, and for limited stage small cell lung cancer (SCLC) it was 59%; these sensitivity values were considerably higher than for traditional biomarkers (including CEA, NSE and CYFRA21-1). Importantly, the combination of the 7-AABs panel and low-dose computed tomography (CT) scanning significantly improved the diagnostic yield in patients presenting with GGNs and/or solid nodules. In conclusion, our 7-AABs panel has clinical value for early detection of lung cancer, including early-stage lung cancer presenting as GGNs.
AB - We have previously identified a panel of autoantibodies (AABs), including p53, GAGE7, PGP9.5, CAGE, MAGEA1, SOX2 and GBU4-5, that was helpful in the early diagnosis of lung cancer. This large-scale, multicenter study was undertaken to validate the clinical value of this 7-AABs panel for early detection of lung cancer in a Chinese population. Two independent sets of plasma samples from 2308 participants were available for the assay of AABs (training set = 300; validation set = 2008). The concentrations of AABs were quantitated by enzyme-linked immunosorbent assay (ELISA), and the optimal cutoff value for each AAB was determined in the training set and then applied in the validation set. The value of the 7-AABs panel for the early detection of lung cancer was assessed in 540 patients who presented with ground-glass nodules (GGNs) and/or solid nodules. In the validation set, the sensitivity and specificity of the 7-AABs panel were 61% and 90%, respectively. For stage I and stage II non-small cell lung cancer (NSCLC), the sensitivity of the 7-AABs panel was 62% and 59%, respectively, and for limited stage small cell lung cancer (SCLC) it was 59%; these sensitivity values were considerably higher than for traditional biomarkers (including CEA, NSE and CYFRA21-1). Importantly, the combination of the 7-AABs panel and low-dose computed tomography (CT) scanning significantly improved the diagnostic yield in patients presenting with GGNs and/or solid nodules. In conclusion, our 7-AABs panel has clinical value for early detection of lung cancer, including early-stage lung cancer presenting as GGNs.
KW - Autoantibody
KW - Biomarker
KW - Early detection
KW - Lung cancer
KW - Tumor-associated antigen
UR - http://www.scopus.com/inward/record.url?scp=85031503688&partnerID=8YFLogxK
U2 - 10.1080/2162402X.2017.1384108
DO - 10.1080/2162402X.2017.1384108
M3 - Article
C2 - 29308305
AN - SCOPUS:85031503688
SN - 2162-4011
VL - 7
JO - OncoImmunology
JF - OncoImmunology
IS - 2
M1 - e1384108
ER -