# Psychological and quality of life outcomes associated with multikinase inhibitors versus immune checkpoint inhibitors in advanced hepatocellular carcinoma

**Authors:** Maher Hendi, Jie-Min Lv, Mohamad Hndi, Bin Zhang, Xue-Qin Chen, Ying-Ying Chen, Yu Pan, Xiu-Jun Cai

PMC · DOI: 10.1038/s41598-026-39864-y · 2026-02-12

## TL;DR

This study found that immune checkpoint inhibitors improve mental health, quality of life, and survival in advanced liver cancer patients compared to multikinase inhibitors.

## Contribution

The study provides new evidence on the psychological and quality of life benefits of immune checkpoint inhibitors over multikinase inhibitors in advanced hepatocellular carcinoma.

## Key findings

- PD-1/PD-L1 inhibitors reduced anxiety and depression more than multikinase inhibitors at 6 months.
- Patients on PD-1/PD-L1 inhibitors had better quality of life and longer survival times.
- Fatigue was a significant predictor of depression, and immune-related side effects lowered quality of life.

## Abstract

To compare the effects of multikinase inhibitors (sorafenib/lenvatinib) and immune checkpoint inhibitors (PD-1/PD-L1) on anxiety, depression, and quality of life (QoL) in patients with advanced hepatocellular carcinoma (HCC) and to analyse their correlations with clinical indicators. This retrospective cohort study included 304 patients with advanced HCC (BCLC stage B/C) who received first-line monotherapy between 2018 and 2023. Propensity score matching (1:1) was used to categorize patients into two groups: those treated with multikinase inhibitors (n = 152) and those treated with PD-1/PD-L1 inhibitors (n = 152). Anxiety and depression (Hospital Anxiety and Depression Scale (HADS)), and QoL (EORTC QLQ-C30) were assessed at baseline and during follow-up (every 3 months). Correlations between the treatment duration, survival outcomes, and adverse events (AEs) were analysed. The PD-1/PD-L1 group presented significant reductions in anxiety (HADS-A: mean difference [MD] = − 2.4) and depression (HADS-D: MD = − 2.3) at 6 months (both *p < 0.001), with lower rates of clinically significant anxiety (28.3% vs. 42.1%) and depression (24.3% vs. 38.8%; p < 0.05). QoL improved markedly (6-month MD = + 10.3, p < 0.001), particularly when the treatment was administered as the first-line therapy (MD = + 14.2 vs. second-line MD = + 3.8; interaction p < 0.001). PD-1/PD-L1 inhibitors were associated with longer treatment durations (median 9.5 vs. 5.8 months, p < 0.001) and superior overall survival (median 18.2 vs. 12.5 months; HR = 0.62, p = 0.002). Fatigue (grade ≥ 2) independently predicted depression (OR = 1.82, p = 0.002), whereas immune-related AEs were correlated with a reduced QoL (ρ=−0.22, p = 0.004). Compared with multikinase inhibitors, PD-1/PD-L1 inhibitors significantly improve the psychological outcomes, QoL, and survival of patients with advanced HCC, especially when administered as first-line therapies. Fatigue is a critical modifiable risk factor for depression. These findings support prioritizing immunotherapy when treating atients with advanced hepatocellular carcinoma.

The online version contains supplementary material available at 10.1038/s41598-026-39864-y.

## Linked entities

- **Chemicals:** sorafenib (PubChem CID 216239), lenvatinib (PubChem CID 9823820)
- **Diseases:** hepatocellular carcinoma (MONDO:0007256), anxiety (MONDO:0005618), depression (MONDO:0002050)

## Full-text entities

- **Genes:** CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}
- **Diseases:** Fatigue (MESH:D005221), HCC (MESH:D006528), Anxiety and Depression (MESH:D001007), depression (MESH:D003866)
- **Chemicals:** multikinase inhibitors (-), sorafenib (MESH:D000077157), lenvatinib (MESH:C531958)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12976292/full.md

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Source: https://tomesphere.com/paper/PMC12976292