TY - JOUR
T1 - Precision pathology analysis of the development and progression of hepatocellular carcinoma
T2 - Implication for precision diagnosis of hepatocellular carcinoma
AU - Ueno, Akihisa
AU - Masugi, Yohei
AU - Yamazaki, Ken
AU - Kurebayashi, Yutaka
AU - Tsujikawa, Hanako
AU - Effendi, Kathryn
AU - Ojima, Hidenori
AU - Sakamoto, Michiie
N1 - Funding Information:
Michiie Sakamoto was the winner of The Japanese Society of Pathology; Japan Pathology Award in 2017. This review article was prepared based on the data presented at the 106th Annual Meeting of the Japanese Society of Pathology, Tokyo, 28 April 2017. The authors would like to thank Naoto Kubota, Mami Hatano, Miho Kawaida, Yoko Nishimura, Katsura Emoto, Kazuhiro Yamanoi, Tokiya Abe, Akinori Hashiguchi and Mariko Fukuma at the Department of Pathology, Keio University School of Medicine, for their valuable scientific help.
Publisher Copyright:
© 2020 Japanese Society of Pathology and John Wiley & Sons Australia, Ltd
PY - 2020/3/1
Y1 - 2020/3/1
N2 - Outcomes for patients with hepatocellular carcinoma (HCC) remain poor because the condition is often unresponsive to the available treatments. Consequently, the early and precise diagnosis of HCC is crucial to achieve improvements in prognosis. For patients with chronic liver disease, the assessment of liver fibrosis is also important to ascertain both the staging of fibrosis and the risk of HCC occurrence. Early HCC was first described in 1991 in Japan and was defined internationally in 2009. As the concept of early HCC spread, the multistage hepatocarcinogenesis process became accepted. Consequently, improvements in imaging technology made the early diagnosis of HCC possible. At present, the most appropriate therapeutic strategy for HCC is determined using an integrated staging system that assesses the tumor burden, the degree of liver dysfunction and the patient performance status; however, pathological and molecular features are not taken into account. The recent introduction of several new therapeutic agents will change the treatment strategy for HCC. Against this background, HCC subclassification based on tumor cellular and microenvironmental characteristics will become increasingly important. In this review, we give an overview of how pathological analysis contributes to understanding the development and progression of HCC and establishing a precision diagnosis of HCC.
AB - Outcomes for patients with hepatocellular carcinoma (HCC) remain poor because the condition is often unresponsive to the available treatments. Consequently, the early and precise diagnosis of HCC is crucial to achieve improvements in prognosis. For patients with chronic liver disease, the assessment of liver fibrosis is also important to ascertain both the staging of fibrosis and the risk of HCC occurrence. Early HCC was first described in 1991 in Japan and was defined internationally in 2009. As the concept of early HCC spread, the multistage hepatocarcinogenesis process became accepted. Consequently, improvements in imaging technology made the early diagnosis of HCC possible. At present, the most appropriate therapeutic strategy for HCC is determined using an integrated staging system that assesses the tumor burden, the degree of liver dysfunction and the patient performance status; however, pathological and molecular features are not taken into account. The recent introduction of several new therapeutic agents will change the treatment strategy for HCC. Against this background, HCC subclassification based on tumor cellular and microenvironmental characteristics will become increasingly important. In this review, we give an overview of how pathological analysis contributes to understanding the development and progression of HCC and establishing a precision diagnosis of HCC.
KW - HCC
KW - computational pathology
KW - early HCC
KW - fibrous stroma
KW - immune microenvironment
KW - molecular diagnosis
KW - molecular marker
KW - molecular subclass
KW - multistage hepatocarcinogenesis
KW - patho-radiological correlation
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U2 - 10.1111/pin.12895
DO - 10.1111/pin.12895
M3 - Review article
C2 - 31908112
AN - SCOPUS:85078061335
SN - 1320-5463
VL - 70
SP - 140
EP - 154
JO - Pathology international
JF - Pathology international
IS - 3
ER -