TY - JOUR
T1 - Detection of early-stage hepatocellular carcinoma in asymptomatic HBsAg-seropositive individuals by liquid biopsy
AU - Qu, Chunfeng
AU - Wang, Yuting
AU - Wang, Pei
AU - Chen, Kun
AU - Wang, Minjie
AU - Zeng, Hongmei
AU - Lu, Jianquan
AU - Song, Qianqian
AU - Diplas, Bill H.
AU - Tan, Da
AU - Fan, Chunsun
AU - Guo, Qigao
AU - Zhu, Zheng
AU - Yin, Huihui
AU - Jiang, Liping
AU - Chen, Xixi
AU - Zhao, Hui
AU - He, Huan
AU - Wang, Yong
AU - Li, Guangyu
AU - Bi, Xinyu
AU - Zhao, Xinming
AU - Chen, Taoyang
AU - Tang, Hongping
AU - Lv, Chuanguo
AU - Wang, Dongmei
AU - Chen, Wanqing
AU - Zhou, Jianguo
AU - Zhao, Hong
AU - Cai, Jianqiang
AU - Wang, Xiaoyue
AU - Wang, Sizhen
AU - Yan, Hai
AU - Zeng, Yi Xin
AU - Cavenee, Webster K.
AU - Jiao, Yuchen
N1 - Publisher Copyright:
© 2019 National Academy of Sciences. All Rights Reserved.
PY - 2019
Y1 - 2019
N2 - Liquid biopsies, based on cell free DNA (cfDNA) and proteins, have shown the potential to detect early stage cancers of diverse tissue types. However, most of these studies were retrospective, using individuals previously diagnosed with cancer as cases and healthy individuals as controls. Here, we developed a liquid biopsy assay, named the hepatocellular carcinoma screen (HCCscreen), to identify HCC from the surface antigen of hepatitis B virus (HBsAg) positive asymptomatic individuals in the community population. The training cohort consisted of individuals who had liver nodules and/or elevated serum α-fetoprotein (AFP) levels, and the assay robustly separated those with HCC from those who were non-HCC with a sensitivity of 85% and a specificity of 93%. We further applied this assay to 331 individuals with normal liver ultrasonography and serum AFP levels. A total of 24 positive cases were identified, and a clinical follow-up for 6-8 mo confirmed four had developed HCC. No HCC cases were diagnosed from the 307 test-negative individuals in the follow-up during the same timescale. Thus, the assay showed 100% sensitivity, 94% specificity, and 17% positive predictive value in the validation cohort. Notably, each of the four HCC cases was at the early stage (<3 cm) when diagnosed. Our study provides evidence that the use of combined detection of cfDNA alterations and protein markers is a feasible approach to identify early stage HCC from asymptomatic community populations with unknown HCC status.
AB - Liquid biopsies, based on cell free DNA (cfDNA) and proteins, have shown the potential to detect early stage cancers of diverse tissue types. However, most of these studies were retrospective, using individuals previously diagnosed with cancer as cases and healthy individuals as controls. Here, we developed a liquid biopsy assay, named the hepatocellular carcinoma screen (HCCscreen), to identify HCC from the surface antigen of hepatitis B virus (HBsAg) positive asymptomatic individuals in the community population. The training cohort consisted of individuals who had liver nodules and/or elevated serum α-fetoprotein (AFP) levels, and the assay robustly separated those with HCC from those who were non-HCC with a sensitivity of 85% and a specificity of 93%. We further applied this assay to 331 individuals with normal liver ultrasonography and serum AFP levels. A total of 24 positive cases were identified, and a clinical follow-up for 6-8 mo confirmed four had developed HCC. No HCC cases were diagnosed from the 307 test-negative individuals in the follow-up during the same timescale. Thus, the assay showed 100% sensitivity, 94% specificity, and 17% positive predictive value in the validation cohort. Notably, each of the four HCC cases was at the early stage (<3 cm) when diagnosed. Our study provides evidence that the use of combined detection of cfDNA alterations and protein markers is a feasible approach to identify early stage HCC from asymptomatic community populations with unknown HCC status.
KW - Cell free DNA
KW - Early detection of cancer
KW - HBsAg-seropositive
KW - Hepatocellular carcinoma
UR - http://www.scopus.com/inward/record.url?scp=85063941524&partnerID=8YFLogxK
U2 - 10.1073/pnas.1819799116
DO - 10.1073/pnas.1819799116
M3 - Article
C2 - 30858324
AN - SCOPUS:85063941524
SN - 0027-8424
VL - 116
SP - 6308
EP - 6312
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 13
ER -