# The Natural History and Prognostic Determinants of Untreated Hepatocellular Carcinoma in a Sub-Saharan African Cohort

**Authors:** Sanju Sobnach, Urda Kotze, C. Wendy Spearman, Mark W. Sonderup, Inae Kim, Keith Venter, René Krause, Muhammad Emmamally, Marc Bernon, Tinus du Toit, Luiz F. Zerbini, Eduard Jonas

PMC · DOI: 10.1007/s12029-026-01414-0 · 2026-02-20

## TL;DR

This study examines the progression and survival rates of untreated liver cancer in a sub-Saharan African cohort, highlighting advanced disease presentation and poor outcomes.

## Contribution

The study provides new insights into the natural history and survival predictors of untreated hepatocellular carcinoma in a sub-Saharan African population.

## Key findings

- Median overall survival was 36.5 days with poor long-term survival rates.
- Chronic hepatitis B virus infection was the leading cause of hepatocellular carcinoma.
- Advanced disease presentation and poor clinical indicators were strong predictors of mortality.

## Abstract

Data on the natural history of untreated hepatocellular carcinoma (HCC) are limited and derive mostly from patients in untreated arms of randomised control trials, conducted in high income countries. In this study, we determined the natural history of untreated HCC and identify predictors of survival in a predominantly SSA cohort of patients managed at Groote Schuur Hospital, Cape Town, South Africa.

A 35-year retrospective cohort study of 469 patients with untreated HCC managed at Groote Schuur Hospital, Cape Town, South Africa from 1990 to 2025 was conducted. Demographics, clinical features, laboratory data, radiological findings and survival were analysed. Multivariate Cox regression identified independent predictors of mortality.

The cohort comprised 347 (74%) men, with a median age of 48 [19–89] years. The majority (380/469, 81.0%) were from South Africa, while the remaining 89 patients originated mostly from other neighbouring SSA countries. Chronic hepatitis B virus (HBV) infection was the leading aetiology (53.3%). Most (96.3%) presented with advanced disease (BCLC stage C or D), with high rates of multifocal tumours (69.1%), portal vein tumour thrombosis (38.8%) and extrahepatic metastases (32.6%). The median overall survival was 36.5 days and the one, six and 12-month survival rates were 59.8%, 14.4% and 7.6% respectively. Independent predictors of mortality included poor performance status, elevated alpha-fetoprotein levels, hypoalbuminemia, higher CTP grade, elevated MELD-Na and advanced BCLC stage.

Untreated HCC in sub-Saharan Africa is marked by advanced presentation and aggressive disease with rapid clinical deterioration and poor long-term survival. This study highlights the critical need for earlier diagnosis, HBV prevention and the development of accessible, early context-appropriate palliative care interventions in resource-limited settings.

• In a sub-Saharan cohort, most patients with untreated hepatocellular carcinoma present with advanced-stage disease.

• Chronic hepatitis B virus infection is the predominant aetiology and associated with multifocal tumours, macrovascular invasion and extrahepatic metastases.

• In patients who receive best supportive care only, there is rapid clinical deterioration and very poor long-term survival.

## Linked entities

- **Diseases:** hepatocellular carcinoma (MONDO:0007256), hepatitis B virus infection (MONDO:0005344)

## Full-text entities

- **Genes:** ALPP (alkaline phosphatase, placental) [NCBI Gene 250] {aka ALP, PALP, PLAP, PLAP-1}, GGTLC5P (gamma-glutamyltransferase light chain 5 pseudogene) [NCBI Gene 653590] {aka GGT}, GGT1 (gamma-glutamyltransferase 1) [NCBI Gene 2678] {aka CD224, D22S672, D22S732, GGT, GGT 1, GGTD}, AFP (alpha fetoprotein) [NCBI Gene 174] {aka AFPD, FETA, HPAFP}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** jaundice (MESH:D007565), hypoalbuminemia (MESH:D034141), splenomegaly (MESH:D013163), extrahepatic (MESH:D001651), pain (MESH:D010146), cirrhotic (MESH:D000094724), Hepatic Vein Tumour Thrombosis (MESH:D006502), REDCap (MESH:D014947), liver disease (MESH:D008107), Cirrhosis (MESH:D005355), varices (MESH:D014648), liver cirrhosis (MESH:D008103), HBV infection (MESH:D006509), Central Nervous System (MESH:D002493), Portal vein tumour thrombosis (MESH:D009369), Chronic hepatitis B virus (HBV) infection (MESH:D019694), HICs (MESH:D008228), fibrolamellar HCC (MESH:C537258), BCLC (MESH:D006528), multifocal (MESH:D000080364), hepatomegaly (MESH:D006529), ascites (MESH:D001201), BSC (MESH:D057826), portal hypertension (MESH:D006975), End-Stage Liver Disease (MESH:D058625), metastases (MESH:D009362), weight loss (MESH:D015431), Child Turcotte Pugh (MESH:C562515)
- **Chemicals:** atezolizumab (MESH:C000594389), bevacizumab (MESH:D000068258), sorafenib (MESH:D000077157), Bilirubin (MESH:D001663), durvalumab (MESH:C000613593), lenvatinib (MESH:C531958), tremelimumab (MESH:C520704), nivolumab (MESH:D000077594), alcohol (MESH:D000438), Na (MESH:D012964), CTP (MESH:D003570), BSC (-), regorafenib (MESH:C559147), pembrolizumab (MESH:C582435)
- **Species:** Hepatitis B virus (no rank) [taxon 10407], Human immunodeficiency virus 1 (no rank) [taxon 11676], hepatitis C virus [taxon 11103], Human immunodeficiency virus (species) [taxon 12721], Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12923431/full.md

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Source: https://tomesphere.com/paper/PMC12923431