Prevalence and clinical characteristics of patients with brain metastases at diagnosis with advanced hepatocellular carcinoma in a retrospective registry.

Q Quincy Harris (Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA) J Jocelin Chen (Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA) J Joseph McGuire (University of California, San Francisco Helen Diller Family Comprehensive Cancer Center, San Francisco, CA) J John Gordan (University of California-San Francisco, San Francisco, CA) H Huat Chye Lim (University of California, San Francisco, San Francisco, CA) M Michael Li (Center for Computational Medicine, Research Institute, Hospital for Sick Children, Toronto) A Alan P. Venook (University of California, San Francisco, San Francisco, CA) A Ann C Griffin (University of California, San Francisco Helen Diller Family Comprehensive Cancer Center, San Francisco, CA) R Robin Kate Kelley (UCSF Comprehensive Cancer Center, San Francisco, CA)

Abstract

540 Background: Hepatocellular carcinoma (HCC) is a cancer with poor prognosis and rising incidence. The combination of atezolizumab plus bevacizumab (A+B) prolongs survival as 1 st line therapy in advanced HCC (aHCC) but confers a rare risk of serious bleeding. HCC brain metastases (BM) have high hemorrhage rates and contraindicate the A+B regimen. Alternative immunotherapies also prolong survival without increased bleeding risk. We conducted a retrospective review of a large, diverse, cancer center registry to estimate the prevalence of and identify clinical characteristics associated with BM in aHCC. Methods: The University of California, San Francisco (UCSF) Helen Diller Family Comprehensive Cancer Center (HDFCCC) registry was queried for new cases of HCC between 2004 and 2022. AJCC stage III or IV were defined as aHCC. Cases with central nervous system (CNS) metastases (including brain as well as skull, face, or orbit as adjacent high-risk sites) at diagnosis were identified. Key clinical covariates including demographics, liver disease etiology, and symptomatology were described. Results: Among 4002 new HCC cases, 832 were classified as aHCC. 12/832 (1.4%, 95% CI: 0.8, 2.5) had synchronous BM. Key demographics are displayed in Table. 10/12 (83%) patients with BM were symptomatic, including headache (25%), neurologic deficits (67%), and/or syncope (8%). Bleeding complications and/or hemorrhagic features were reported in 17%. Conclusions: BM are rare at diagnosis with aHCC, present in only 1.4% of this registry dataset. The majority (83%) were symptomatic, suggesting that routine CNS imaging may not have clinical utility in asymptomatic patients. A high proportion with BM at diagnosis had viral etiology. Limitations of this retrospective registry analysis include potential for underdiagnosis in asymptomatic patients and incomplete data for clinical covariates. Clinical characteristics of aHCC cases with BM at diagnosis between 2004-2022 in UCSF HDFCCC Registry. Overall aHCC Cases (N=832) Cases with BM (n=12) Median age (range) (yrs.) 61 (8-92) 60 (48-65) Race/ethnicity (%)AsianBlackCaucasianHispanic (any race) 29105715 2586717 Gender (%)MaleFemale 7921 7525 Etiology (%)Viral hepatitisUnknown/negative 2971 7525 Symptomatic BM (%)HeadacheNeurologic deficitsSyncope NA 8325678 Hemorrhagic BM (%) NA 17

Article Details

Volume / Issue Vol. 43, Issue 4_suppl
Published February 01, 2025
Pages 540-540
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (9)

Q

Quincy Harris

Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA

J

Jocelin Chen

Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA

J

Joseph McGuire

University of California, San Francisco Helen Diller Family Comprehensive Cancer Center, San Francisco, CA

J

John Gordan

University of California-San Francisco, San Francisco, CA

H

Huat Chye Lim

University of California, San Francisco, San Francisco, CA

M

Michael Li

Center for Computational Medicine, Research Institute, Hospital for Sick Children, Toronto

A

Alan P. Venook

University of California, San Francisco, San Francisco, CA

A

Ann C Griffin

University of California, San Francisco Helen Diller Family Comprehensive Cancer Center, San Francisco, CA

R

Robin Kate Kelley

UCSF Comprehensive Cancer Center, San Francisco, CA