# Physical Activity and Hepatocellular Carcinoma Outcomes: a Narrative Review of Pre-clinical, Observational, and Interventional Evidence

**Authors:** Nadia Kim, Lisa Alcock, Silvia Del Din, Helen L. Reeves, Samuel T. Orange

PMC · DOI: 10.1007/s12029-026-01420-2 · Journal of Gastrointestinal Cancer · 2026-03-05

## TL;DR

This review explores how physical activity might improve outcomes for people with liver cancer, suggesting it could help with treatment tolerance, quality of life, and survival.

## Contribution

The paper provides a narrative synthesis of pre-clinical, observational, and interventional evidence supporting physical activity in hepatocellular carcinoma care.

## Key findings

- Pre-clinical studies suggest physical activity enhances anti-tumor responses via metabolic and immune mechanisms.
- Observational studies link reduced physical function with shorter survival in HCC patients.
- Exercise programs may improve frailty and preserve muscle mass in HCC patients.

## Abstract

Hepatocellular carcinoma (HCC) is a leading cause of cancer-related mortality worldwide, with incidence and mortality projected to rise. Most patients present with advanced or unresectable disease, where treatment efficacy is often constrained by frailty and impaired physical function. As physical function has emerged as a key determinant of treatment eligibility and survival, there is growing interest in physical activity as a supportive intervention in HCC care.

This narrative review synthesises observational, pre-clinical, and trial evidence on the role of physical activity in patients with HCC, examining its potential to improve treatment tolerance, quality of life, and survival.

A literature search was conducted across four databases (PubMed, Scopus, Web of Science, Embase) using keywords related to HCC, physical activity, exercise, and survivorship.

Pre-clinical studies reveal multiple mechanisms through which physical activity may enhance anti-tumour responses, including metabolic reprogramming, modulation of oncogenic signalling and immune activation. Observational studies suggest that frailty and sarcopenia - markers of reduced physical function, are possibly associated with early treatment discontinuation and shorter survival in HCC. Preliminary interventional data suggest that structured exercise programmes, delivered in hospital, outpatient, telehealth, or mobile formats, can improve frailty, preserve muscle mass, and may potentially support survival. However, clinical studies to date are limited by small sample sizes, non-randomised designs, and short follow-up periods.

Current evidence provides a biologically plausible and clinically promising rationale for integrating physical activity into HCC care pathways. While findings are encouraging, robust randomised trials are needed to establish efficacy, define optimal exercise regimens, and evaluate long-term outcomes.

## Linked entities

- **Diseases:** hepatocellular carcinoma (MONDO:0007256), HCC (MONDO:0007256)

## Full-text entities

- **Genes:** STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, Stat3 (signal transducer and activator of transcription 3) [NCBI Gene 25125], INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, PRKAB1 (protein kinase AMP-activated non-catalytic subunit beta 1) [NCBI Gene 5564] {aka AMPK, HAMPKb}, Pten (phosphatase and tensin homolog) [NCBI Gene 50557] {aka MMAC1, Mmac, TEP1}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, Tigit (T cell immunoreceptor with Ig and ITIM domains) [NCBI Gene 100043314] {aka Vstm3}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, PTEN (phosphatase and tensin homolog) [NCBI Gene 5728] {aka 10q23del, BZS, CWS1, DEC, GLM2, MHAM}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, Akt1 (AKT serine/threonine kinase 1) [NCBI Gene 24185] {aka Akt}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, Ctla4 (cytotoxic T-lymphocyte-associated protein 4) [NCBI Gene 12477] {aka Cd152, Ctla-4, Ly-56}, PDCD1 (programmed cell death 1) [NCBI Gene 100533201], ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, Prkaa2 (protein kinase AMP-activated catalytic subunit alpha 2) [NCBI Gene 78975] {aka Ampk, Ampka2}, PTK2B (protein tyrosine kinase 2 beta) [NCBI Gene 2185] {aka CADTK, CAKB, FADK2, FAK2, PKB, PTK}, Havcr2 (hepatitis A virus cellular receptor 2) [NCBI Gene 171285] {aka TIM-3, Tim3, Timd3}
- **Diseases:** impaired physical function (MESH:D059445), Steatotic Liver Disease (MESH:D008107), sarcopenia (MESH:D055948), Inflammation (MESH:D007249), variceal bleeding (MESH:D014648), cirrhosis (MESH:D005355), balance impairment (MESH:D060825), Cancer (MESH:D009369), diabetes (MESH:D003920), carcinogenesis (MESH:D063646), muscle gain (MESH:D015430), bleeding (MESH:D006470), low muscle mass (MESH:C536030), SMI (MESH:D005207), Frailty (MESH:D000073496), Metabolic Dysfunction (MESH:D008659), OS (MESH:C567932), death (MESH:D003643), encephalopathy (MESH:D001927), muscle hypertrophy (MESH:C536106), viral hepatitis (MESH:D014777), ascites (MESH:D001201), metastasis (MESH:D009362), toxicity (MESH:D064420), thrombocytopenia (MESH:D013921), muscle loss (MESH:D009135), anaemia (MESH:D000743), hepatic encephalopathy (MESH:D006501), alcohol-related liver disease (MESH:D008108), hepatic decompensation (MESH:D006333), liver tumour (MESH:D008113), HCC (MESH:D006528), functional limitation (MESH:D045745)
- **Chemicals:** epinephrine (MESH:D004837), TCA (MESH:D014233), bilirubin (MESH:D001663), phospholipid (MESH:D010743), metformin (MESH:D008687), sorafenib (MESH:D000077157), TACE (-), Lenvatinib (MESH:C531958), citric acid (MESH:D019343), glucose (MESH:D005947), DEN (MESH:D004052)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Cell lines:** Morris Hepatoma-3924 A — Rattus norvegicus (Rat), Rat hepatocellular carcinoma, Cancer cell line (CVCL_5799)

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12960373