TY - JOUR
T1 - Clinical Characteristics, Treatment Patterns, and Outcomes of Patients with Locally Advanced/Metastatic Hepatocellular Carcinoma Treated at the Veterans Health Administration
AU - Alkadimi, Munaf A.
AU - Aldawoodi, Tamarah A.
AU - Lucero, Kana T.
AU - Fierro, Maria E.
AU - Boyle, Lauren D.
AU - Mader, Michael J.
AU - Franklin, Kathleen R.
AU - Arora, Sukeshi P.
AU - Nooruddin, Zohra
N1 - Publisher Copyright:
© 2024 Published by Oxford University Press.
PY - 2024/5
Y1 - 2024/5
N2 - Purpose: This study retrospectively reviewed the outcomes of patients with advanced hepatocellular carcinoma (HCC) receiving atezolizumab with bevacizumab (A+B) therapy at the Veterans Health Administration (VHA). Patients and Methods: Patients with advanced HCC who received first-line systemic therapy with A+B at the VHA between December 1, 2019, and March 1, 2022, were selected from electronic medical records (EMR) using ICD-9 and ICD-10 codes. Abstractors reviewed the EMR of the patients from their index date of A+B initiation until death or their last VHA visit, with the study period ending on January 31, 2023. The chi-square test was used to compare rates, and the Mann-Whitney test was used to compare medians. Results: A total of 332 patients met the study criteria. The median age was 67 years; 99% were male, 63% were non-Hispanic Whites, 26% were Black, and 66% had an Eastern Cooperative Oncology Group performance status of ≥1. 84% had child Pugh score (CPS) class A, 16% had CPS classes B and C, 62% had a grade 2 albumin-bilirubin score, 56% had HCC caused by viral hepatitis, 80% had cirrhosis, and 67% had received prior local therapies. The 6-month progression-free survival (PFS) was 59%, while the 1-year PFS rate was 36%. Overall survival (OS) at 1-year was 52% in our study. Conclusion: In real world, despite having similar PFS as the phase III IMbrave 150 trial, our OS at 12 months was lower (52% vs. 67%) because our study included a higher proportion of elderly patients with moderate liver dysfunction and a 40% non-White. This study provided real-world outcomes that differed from the study population in a pivotal trial.
AB - Purpose: This study retrospectively reviewed the outcomes of patients with advanced hepatocellular carcinoma (HCC) receiving atezolizumab with bevacizumab (A+B) therapy at the Veterans Health Administration (VHA). Patients and Methods: Patients with advanced HCC who received first-line systemic therapy with A+B at the VHA between December 1, 2019, and March 1, 2022, were selected from electronic medical records (EMR) using ICD-9 and ICD-10 codes. Abstractors reviewed the EMR of the patients from their index date of A+B initiation until death or their last VHA visit, with the study period ending on January 31, 2023. The chi-square test was used to compare rates, and the Mann-Whitney test was used to compare medians. Results: A total of 332 patients met the study criteria. The median age was 67 years; 99% were male, 63% were non-Hispanic Whites, 26% were Black, and 66% had an Eastern Cooperative Oncology Group performance status of ≥1. 84% had child Pugh score (CPS) class A, 16% had CPS classes B and C, 62% had a grade 2 albumin-bilirubin score, 56% had HCC caused by viral hepatitis, 80% had cirrhosis, and 67% had received prior local therapies. The 6-month progression-free survival (PFS) was 59%, while the 1-year PFS rate was 36%. Overall survival (OS) at 1-year was 52% in our study. Conclusion: In real world, despite having similar PFS as the phase III IMbrave 150 trial, our OS at 12 months was lower (52% vs. 67%) because our study included a higher proportion of elderly patients with moderate liver dysfunction and a 40% non-White. This study provided real-world outcomes that differed from the study population in a pivotal trial.
KW - atezolizumab
KW - bevacizumab
KW - hepatocellular carcinoma
KW - real-world evidence
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U2 - 10.1093/oncolo/oyad343
DO - 10.1093/oncolo/oyad343
M3 - Review article
C2 - 38254242
AN - SCOPUS:85192114005
SN - 1083-7159
VL - 29
SP - 369
EP - 376
JO - Oncologist
JF - Oncologist
IS - 5
ER -