Literature DB >> 34780081

Changes in therapeutic options for hepatocellular carcinoma in Asia.

Sadahisa Ogasawara1,2, Keisuke Koroki1, Hiroaki Kanzaki1, Kazufumi Kobayashi1, Soichiro Kiyono1, Masato Nakamura1, Naoya Kanogawa1, Tomoko Saito1, Takayuki Kondo1, Ryo Nakagawa1, Shingo Nakamoto1, Ryosuke Muroyama1, Tetsuhiro Chiba1, Naoya Kato1.   

Abstract

The incidence rate of hepatocellular carcinoma (HCC) is expected to increase, with most cases occurring in Asia. In some parts of Asia, the occurrence of HCC developing from metabolic-related liver disease has markedly increased in recent years, whereas the occurrence of HCC developing from viral-hepatitis-related liver disease has decreased. Advancements in the treatment of HCC over the past few decades has been remarkable, with most treatment strategies to remove or control liver tumours (hepatic resection, local ablation, radiation therapy, transarterial chemoembolisation, hepatic arterial infusion chemotherapy) primarily developing in Asia. In addition, recent progress in systemic therapies has prolonged the prognosis of advanced HCC. Nowadays, six regimens of systemic therapies have become available in most countries, according to phase III trials (atezolizumab plus bevacizumab, sorafenib, lenvatinib, regorafenib, cabozantinib and ramucirumab). In a global randomised phase III trial (IMbrave 150 trial), the most effective of the latest drug designs was newly emerged combination immunotherapy (atezolizumab plus bevacizumab), which has shown significantly prolonged overall survival compared with sorafenib, which was the first-line systemic therapy for more than a decade. Now, the treatment dynamics for HCC are undergoing a major transition as a result of two important changes: the replacement of viral-related HCC by metabolic-related HCC and the emergence of combination immune therapy.
© 2021 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  hepatic resection; hepatocarcinogenesis; hepatocellular carcinoma; immunotherapy; tumour microenvironment

Mesh:

Substances:

Year:  2021        PMID: 34780081     DOI: 10.1111/liv.15101

Source DB:  PubMed          Journal:  Liver Int        ISSN: 1478-3223            Impact factor:   8.754


  3 in total

1.  Real-world efficacy and safety of cabozantinib in Korean patients with advanced hepatocellular carcinoma: a multicenter retrospective analysis.

Authors:  Yeong Hak Bang; Choong-Kun Lee; Changhoon Yoo; Hong Jae Chon; Moonki Hong; Beodeul Kang; Hyung-Don Kim; Sook Ryun Park; Won-Mook Choi; Jonggi Choi; Danbi Lee; Ju Hyun Shim; Kang Mo Kim; Young-Suk Lim; Han Chu Lee; Min-Hee Ryu; Baek-Yeol Ryoo
Journal:  Ther Adv Med Oncol       Date:  2022-05-14       Impact factor: 5.485

2.  Significance of post-progression therapy after tyrosine kinase inhibitors for advanced hepatocellular carcinoma.

Authors:  Yoshihiko Yano; Atsushi Yamamoto; Akihiro Minami; Kenji Momose; Takuya Mimura; Soo Ki Kim; Hiroki Hayashi; Takuo Kado; Hirotaka Hirano; Seiya Hirohata; Seitetsu Yoon; Katsuhisa Nishi; Hiroshi Tei; Hidenori Tanaka; Sachiko Oouchi; Takanori Matsuura; Eiichiro Yasutomi; Yuri Hatazawa; Yuuki Shiomi; Yoshihide Ueda; Yuzo Kodama
Journal:  JGH Open       Date:  2022-05-25

3.  A Combination of Sorafenib, an Immune Checkpoint Inhibitor, TACE and Stereotactic Body Radiation Therapy versus Sorafenib and TACE in Advanced Hepatocellular Carcinoma Accompanied by Portal Vein Tumor Thrombus.

Authors:  Zeyu Zhang; Chan Li; Weijun Liao; Yun Huang; Zhiming Wang
Journal:  Cancers (Basel)       Date:  2022-07-25       Impact factor: 6.575

  3 in total

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