# Oncolytic virus therapy in the elderly: immune frailty, challenges, and perspectives

**Authors:** Jia-Wen Wang, Jia-Hui Liu, Yue-Lin Liu, Wen-Zheng Xu, Zi-Bo Zhang

PMC · DOI: 10.3389/fimmu.2025.1686659 · Frontiers in Immunology · 2025-10-08

## TL;DR

This paper explores how oncolytic virus therapy can be used to treat cancer in elderly patients, considering their unique immune challenges.

## Contribution

The paper introduces a framework for tailoring oncolytic virus therapies to elderly patients based on immune frailty stages.

## Key findings

- Elderly patients with melanoma/sarcoma showed objective response rates of 26.4–32.9% with oncolytic virus therapy.
- Age-related immune frailty may lead to immune overload and poor tolerance of oncolytic virus treatments.
- Systematic studies on oncolytic virus therapy in elderly populations are currently lacking.

## Abstract

With global aging accelerating, cancer incidence among older adults is rapidly increasing. Individuals aged ≥65 years now represent 64% of new cancer cases and 71.3% of cancer-related deaths worldwide. This population exhibits a distinct immune imbalance—driven by tumor-induced immunosuppression, immunosenescence, and inflammaging—which contributes to poor tolerance of standard therapies and suboptimal outcomes with PD-1/PD-L1 inhibitors.

As an emerging immunotherapeutic strategy, oncolytic viruses (OVs) selectively infect tumor cells, induce immunogenic cell death (ICD), and activate the cGAS–STING pathway. Although clinical data in elderly patients with esophageal, lung, or pancreatic cancer are scarce, promising outcomes have been reported in melanoma/sarcoma subgroups, including objective response rates of 26.4–32.9% and a median duration of response of 33.7 months, highlighting the potent antitumor potential of OVs.

However, age-related immunological vulnerability—manifesting across different frailty stages as reflected by G8 scoring—may predispose elderly patients to immune overload, cytokine storm, and impaired tolerance, while this group remains underrepresented in OV trials. Systematic studies in this context are lacking. This review highlights the immunological characteristics of aging, emphasizes the importance of addressing immunological vulnerability across different age stages (G8 scoring), and outlines emerging challenges and future directions for OV-based therapies tailored to frail elderly populations.

## Linked entities

- **Diseases:** cancer (MONDO:0004992), esophageal cancer (MONDO:0007576), lung cancer (MONDO:0005138), pancreatic cancer (MONDO:0005192), melanoma (MONDO:0005105), sarcoma (MONDO:0005089)

## Full-text entities

- **Genes:** STING1 (stimulator of interferon response cGAMP interactor 1) [NCBI Gene 340061] {aka ERIS, MITA, MPYS, NET23, SAVI, STING}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, CGAS (cyclic GMP-AMP synthase) [NCBI Gene 115004] {aka C6orf150, D4, MB21D1, h-cGAS}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}
- **Diseases:** esophageal, lung, or pancreatic cancer (MESH:D008175), sarcoma (MESH:D012509), melanoma (MESH:D008545), cancer (MESH:D009369)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12540392/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12540392/full.md

## References

133 references — full list in the complete paper: https://tomesphere.com/paper/PMC12540392/full.md

---
Source: https://tomesphere.com/paper/PMC12540392