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Kenji Imai1, Koji Takai1, Shinji Unome1
1Department of Gastroenterology/Internal Medicine, Graduate School of Medicine, Gifu University, 1-1 Yanagido, Gifu 501-1194, Japan.
Atezolizumab plus bevacizumab (AB) maintained skeletal muscle index (SMI) in hepatocellular carcinoma (HCC) patients, unlike lenvatinib (LEN). Preserved SMI is crucial for survival, making AB superior for maintaining muscle health during HCC treatment.
Area of Science:
- Hepatocellular Carcinoma Research
- Oncology Therapeutics
- Body Composition Analysis
Background:
- Hepatocellular carcinoma (HCC) treatments impact patient body composition and biomarkers.
- Skeletal muscle index (SMI) is a potential prognostic factor in cancer patients.
- Understanding treatment-related changes in adipose tissue and tumor markers is vital.
Purpose of the Study:
- To evaluate chronological changes in SMI, adipose tissue indices (SATI, VATI), AFP, PIVKA-II, and ALBI scores during atezolizumab plus bevacizumab (AB) or lenvatinib (LEN) therapy for HCC.
- To determine the effect of these changes on patient survival.
- To identify predictors for survival and changes in SMI during treatment.
Main Methods:
- Analysis of 94 HCC patients (37 on AB, 57 on LEN) with measurements at treatment introduction, 3 months, end of treatment, and last observation.
- Utilized Wilcoxon paired test for chronological change analysis.
- Employed Cox proportional hazards model and analysis of covariance to identify independent predictors for survival and SMI changes.
Main Results:
- SMI was maintained with AB treatment but significantly decreased with LEN treatment.
- SMI, AFP, and ALBI score were independent predictors of survival.
- Drug choice (AB vs. LEN) and PIVKA-II were independent predictors for SMI changes.
Conclusions:
- Atezolizumab plus bevacizumab (AB) is superior to lenvatinib (LEN) in maintaining skeletal muscle index (SMI) during hepatocellular carcinoma (HCC) treatment.
- Maintaining SMI is a critical factor for improving survival outcomes in HCC patients.
- Body composition changes and specific biomarkers should be monitored during HCC therapy.
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