4.6 Review

Immunotherapies for hepatocellular carcinoma

期刊

NATURE REVIEWS CLINICAL ONCOLOGY
卷 19, 期 3, 页码 151-172

出版社

NATURE PORTFOLIO
DOI: 10.1038/s41571-021-00573-2

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资金

  1. European Commission (EC) [667273-2]
  2. US NIH [RO1DK56621, RO1DK128289]
  3. Samuel Waxman Cancer Research Foundation
  4. EIT Health (CRISH2) [18053]
  5. Spanish National Health Institute (MICINN) [PID2019-105378RB-I00]
  6. Cancer Research UK (CRUK)
  7. Fondazione AIRC
  8. Fundacion Cientifica de la Asociacion Espanola Contra el Cancer (HUNTER) [C9380/A26813]
  9. Generalitat de Catalunya (AGAUR) [SGR-1358]
  10. European Research Council (ERC) Consolidator grant (HepatoMetaboPath)
  11. German Research Foundation (Deutsche Forschungsgemeinschaft) [SFB/TR 209, 314905040, 360372040, SFBTR1335]
  12. Rainer Hoenig Foundation
  13. Horizon 2020 Programme grant (HEPCAR)
  14. German Cancer Aid (Deutsche Krebshilfe) [70113166, 70113167]
  15. CRUK Immunology Project [26603]
  16. CRUK Accelerator award HUNTER
  17. Wellcome Trust Strategic Fund [PS3416]
  18. ASCO Conquer Cancer Foundation Global Oncology Young Investigator Award 2019 [14704]
  19. CRUK [C57701/A26137]
  20. CW+
  21. Westminster Medical School Research Trust [JRC SG 009 2018-19]

向作者/读者索取更多资源

Liver cancer, specifically hepatocellular carcinoma (HCC), is the second leading cause of cancer-related death globally. Traditional treatments involve specific drugs, but the emergence of immune checkpoint inhibitors has revolutionized the management of HCC.
Liver cancer, more specifically hepatocellular carcinoma (HCC), is the second leading cause of cancer-related death and its incidence is increasing globally. Around 50% of patients with HCC receive systemic therapies, traditionally sorafenib or lenvatinib in the first line and regorafenib, cabozantinib or ramucirumab in the second line. In the past 5 years, immune-checkpoint inhibitors have revolutionized the management of HCC. The combination of atezolizumab and bevacizumab has been shown to improve overall survival relative to sorafenib, resulting in FDA approval of this regimen. More recently, durvalumab plus tremelimumab yielded superior overall survival versus sorafenib and atezolizumab plus cabozantinib yielded superior progression-free survival. In addition, pembrolizumab monotherapy and the combination of nivolumab plus ipilimumab have received FDA Accelerated Approval in the second-line setting based on early efficacy data. Despite these major advances, the molecular underpinnings governing immune responses and evasion remain unclear. The immune microenvironment has crucial roles in the development and progression of HCC and distinct aetiology-dependent immune features have been defined. Inflamed and non-inflamed classes of HCC and genomic signatures have been associated with response to immune-checkpoint inhibitors, yet no validated biomarker is available to guide clinical decision-making. This Review provides information on the immune microenvironments underlying the response or resistance of HCC to immunotherapies. In addition, current evidence from phase III trials on the efficacy, immune-related adverse events and aetiology-dependent mechanisms of response are described. Finally, we discuss emerging trials assessing immunotherapies across all stages of HCC that might change the management of this disease in the near future. Immunotherapy is revolutionizing the treatment of many cancers and hepatocellular carcinoma (HCC) is no exception. This Review describes the heterogeneous immune microenvironments of HCC as well as their links with the various aetiologies underlying this malignancy and with response or resistance to immunotherapies. In addition, the authors provide an overview of the current landscape of clinical trials evaluating immunotherapies across all stages of HCC.

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