Hepatitis C-positive Black patients develop hepatocellular carcinoma at earlier stages of liver disease and present with a more aggressive phenotype.


Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
01 05 2021
Historique:
revised: 28 08 2020
received: 24 07 2020
accepted: 07 09 2020
pubmed: 26 2 2021
medline: 16 11 2021
entrez: 25 2 2021
Statut: ppublish

Résumé

In the United States, mortality after a diagnosis of hepatocellular carcinoma (HCC) is higher in patients who are Black than in patients of other racial groups. The objective of this study was to clarify factors contributing to this disparity by analyzing liver and tumor characteristics in patients with HCC who have a history of hepatitis C virus (HCV) infection. Records of patients with HCV and HCC at the authors' institution from 2003 to 2018 were retrospectively reviewed. Race and ethnicity were self-identified. Imaging, laboratory, and pathologic features were compared between Black and non-Black cohorts. Among 1195 individuals with HCC, 390 identified as Black. At the time of HCC diagnosis, Black patients had better liver function, as measured by Child-Pugh score, Model of End-Stage Liver Disease score, histology of nontumor tissue, and fibrosis-4 (FIB-4) score (all P < .05). FIB-4 scores were <3.25 in 31% of Black patients. In addition, Black patients had less early stage HCC (20.2% vs 32.3%; P < .05), larger tumors (median [interquartile range]: 3.5 cm [2.2-6.2 cm] vs 3.1 cm [2.1-5.1 cm]; P < .01), more multiple tumors (median, [interquartile range]: 1 tumor [1-3 tumors] vs 1 tumor [1-2 tumors]; P = .03), more poorly differentiated tumors (30.3% vs 20.5%; P < .05), and more microvascular invasion (67.2% vs 56.5%; P < .05). Black patients with HCV exposure develop HCC at earlier stages of liver disease than members of other racial groups. Nearly one-third would not qualify for HCC screening using the common FIB-4 cirrhosis threshold. Practice guidelines that stress HCC surveillance for cirrhotic patients with HCV may need to be revised to be more inclusive for Black patients. In addition, tumors in Black patients carry worse prognostic features, and molecular studies are needed to characterize their biologic properties.

Sections du résumé

BACKGROUND
In the United States, mortality after a diagnosis of hepatocellular carcinoma (HCC) is higher in patients who are Black than in patients of other racial groups. The objective of this study was to clarify factors contributing to this disparity by analyzing liver and tumor characteristics in patients with HCC who have a history of hepatitis C virus (HCV) infection.
METHODS
Records of patients with HCV and HCC at the authors' institution from 2003 to 2018 were retrospectively reviewed. Race and ethnicity were self-identified. Imaging, laboratory, and pathologic features were compared between Black and non-Black cohorts.
RESULTS
Among 1195 individuals with HCC, 390 identified as Black. At the time of HCC diagnosis, Black patients had better liver function, as measured by Child-Pugh score, Model of End-Stage Liver Disease score, histology of nontumor tissue, and fibrosis-4 (FIB-4) score (all P < .05). FIB-4 scores were <3.25 in 31% of Black patients. In addition, Black patients had less early stage HCC (20.2% vs 32.3%; P < .05), larger tumors (median [interquartile range]: 3.5 cm [2.2-6.2 cm] vs 3.1 cm [2.1-5.1 cm]; P < .01), more multiple tumors (median, [interquartile range]: 1 tumor [1-3 tumors] vs 1 tumor [1-2 tumors]; P = .03), more poorly differentiated tumors (30.3% vs 20.5%; P < .05), and more microvascular invasion (67.2% vs 56.5%; P < .05).
CONCLUSIONS
Black patients with HCV exposure develop HCC at earlier stages of liver disease than members of other racial groups. Nearly one-third would not qualify for HCC screening using the common FIB-4 cirrhosis threshold. Practice guidelines that stress HCC surveillance for cirrhotic patients with HCV may need to be revised to be more inclusive for Black patients. In addition, tumors in Black patients carry worse prognostic features, and molecular studies are needed to characterize their biologic properties.

Identifiants

pubmed: 33629759
doi: 10.1002/cncr.33377
pmc: PMC8084866
mid: NIHMS1629928
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1395-1406

Subventions

Organisme : NCI NIH HHS
ID : R03 CA164546
Pays : United States
Organisme : ACL HHS
ID : U01OH011489
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2021 American Cancer Society.

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Auteurs

Tali Shaltiel (T)

Division of Surgical Oncology, Department of Surgery, Icahn School of Medicine at Mount Sinai, New York, New York.

Serena Zheng (S)

Icahn School of Medicine at Mount Sinai, New York, New York.

Cleo Siderides (C)

Icahn School of Medicine at Mount Sinai, New York, New York.

Elizabeth M Gleeson (EM)

Division of Surgical Oncology, Department of Surgery, Icahn School of Medicine at Mount Sinai, New York, New York.

Jacquelyn Carr (J)

Division of Surgical Oncology, Department of Surgery, Icahn School of Medicine at Mount Sinai, New York, New York.

Eric R Pletcher (ER)

Division of Surgical Oncology, Department of Surgery, Icahn School of Medicine at Mount Sinai, New York, New York.

Noah A Cohen (NA)

Division of Surgical Oncology, Department of Surgery, Icahn School of Medicine at Mount Sinai, New York, New York.

Benjamin J Golas (BJ)

Division of Surgical Oncology, Department of Surgery, Icahn School of Medicine at Mount Sinai, New York, New York.

Deepa R Magge (DR)

Division of Surgical Oncology, Department of Surgery, Icahn School of Medicine at Mount Sinai, New York, New York.

Daniel M Labow (DM)

Division of Surgical Oncology, Department of Surgery, Icahn School of Medicine at Mount Sinai, New York, New York.

Andrea D Branch (AD)

Division of Liver Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.

Umut Sarpel (U)

Division of Surgical Oncology, Department of Surgery, Icahn School of Medicine at Mount Sinai, New York, New York.

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