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Outcomes of Patients with Child-Pugh B and Unresectable Hepatocellular Carcinoma Undergoing First-Line Systemic Treatment with Sorafenib, Lenvatinib, or Atezolizumab Plus Bevacizumab.

Authors :
Kikugawa C
Uchikawa S
Kawaoka T
Kinami T
Yano S
Amioka K
Naruto K
Ando Y
Yamaoka K
Tsuge M
Kosaka Y
Ohya K
Mori N
Takaki S
Tsuji K
Kouno H
Kohno H
Morio K
Moriya T
Nonaka M
Aisaka Y
Masaki K
Honda Y
Naeshiro N
Hiramatsu A
Aikata H
Oka S
Source :
Oncology [Oncology] 2024; Vol. 102 (3), pp. 239-251. Date of Electronic Publication: 2023 Sep 20.
Publication Year :
2024

Abstract

Introduction: Systemic therapy is recommended for patients with Child-Pugh A in hepatocellular carcinoma (HCC). We analyzed the outcomes of a cohort of patients with HCC who received either sorafenib (Sor), lenvatinib (Len) or atezolizumab plus bevacizumab (Atezo + Bev) as first-line systemic therapy for HCC, with the aim of identifying prognostic factors for survival.<br />Methods: A total of 825 patients with advanced HCC and Child-Pugh A or B received either Sor, Len or Atezo + Bev as first-line systemic therapy. Liver function was assessed according to the Child-Pugh score and the modified albumin-bilirubin (mALBI) grade.<br />Results: Prognosis was analyzed according to liver function such as Child-Pugh classifications, scores, and mALBI grades that worsened with a decline in liver function (p <0.001 for all). A Child-Pugh score of 7 was a factor significantly associated with OS. In patients with a Child-Pugh score of 7, an mALBI grade of 3 was an independent predictor of OS. In Child-Pugh B patients with HCC, receiving Atezo + Bev was identified as a factor associated with PFS.<br />Conclusion: Determining the hepatic reserve of patients with unresectable HCC might be useful for identifying patents suitable for systemic treatment for HCC. Atezo + Bev might prolong the PFS of patients with a Child-Pugh score of 7.<br /> (© 2023 S. Karger AG, Basel.)

Details

Language :
English
ISSN :
1423-0232
Volume :
102
Issue :
3
Database :
MEDLINE
Journal :
Oncology
Publication Type :
Academic Journal
Accession number :
37729889
Full Text :
https://doi.org/10.1159/000533859