# Advances in Systemic Therapy for Unresectable Hepatocellular Carcinoma: Commentary on The Impact of the STRIDE Regimen in HIMALAYA Trial

**Authors:** Leenah Abdulgader, Abdullah Esmail

PMC · DOI: 10.32604/or.2026.069227 · Oncology Research · 2026-02-24

## TL;DR

The STRIDE regimen shows a modest survival benefit for advanced liver cancer but comes with higher risks and costs, requiring careful evaluation for broader use.

## Contribution

This commentary evaluates the STRIDE regimen's impact and challenges in treating unresectable hepatocellular carcinoma.

## Key findings

- STRIDE achieved a median overall survival of 16.43 months compared to 13.77 months with sorafenib.
- STRIDE has increased immune-related toxicity and cost, raising concerns about its practical implementation.
- The regimen shows limitations in non-viral HCC and Child-Pugh B patients.

## Abstract

Unresectable hepatocellular carcinoma (HCC) remains a global challenge, with limited effective treatment options for advanced-stage disease. The HIMALAYA trial (phase III randomized study that evaluated the STRIDE regimen) introduced the Single Tremelimumab Regular Interval Durvalumab (STRIDE) regimen, an immunotherapy-based approach that achieved a median overall survival (OS) of 16.43 months compared to 13.77 months with sorafenib. While statistically significant, this ~2.7 months OS gain warrants scrutiny in light of STRIDE’s increased immune-related toxicity and cost. This commentary evaluates STRIDE’s impact within the broader landscape of first-line systemic therapy for unresectable HCC, alongside other regimens such as atezolizumab plus bevacizumab and nivolumab plus ipilimumab. We explore STRIDE’s mechanism of action, safety profile, modest progression-free survival (PFS) improvement, and implementation challenges, incorporating insights from 2023–2025 research. In addition, we discussed its limitations in non-viral HCC and Child-Pugh B patients, the role of emerging biomarkers, and the potential of radiation to enhance immunotherapy efficacy. As a dual immune checkpoint inhibitor (ICI) strategy, STRIDE offers an important advance that may not only extend survival but also open the door to future curative approaches. However, optimizing its use will require refined patient selection and further investigation of synergistic combination therapies.

## Linked entities

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

## Full-text entities

- **Genes:** TXK (TXK tyrosine kinase) [NCBI Gene 7294] {aka BTKL, PSCTK5, PTK4, RLK, TKL}, ZHX2 (zinc fingers and homeoboxes 2) [NCBI Gene 22882] {aka AFR1, RAF}, STING1 (stimulator of interferon response cGAMP interactor 1) [NCBI Gene 340061] {aka ERIS, MITA, MPYS, NET23, SAVI, STING}, RET (ret proto-oncogene) [NCBI Gene 5979] {aka CDHF12, CDHR16, HSCR1, MEN2A, MEN2B, MTC1}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, KDR (kinase insert domain receptor) [NCBI Gene 3791] {aka CD309, FLK1, VEGFR, VEGFR2}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, AFP (alpha fetoprotein) [NCBI Gene 174] {aka AFPD, FETA, HPAFP}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, PDGFRB (platelet derived growth factor receptor beta) [NCBI Gene 5159] {aka CD140B, IBGC4, IMF1, JTK12, KOGS, OPDKD}, KIT (KIT proto-oncogene, receptor tyrosine kinase) [NCBI Gene 3815] {aka C-Kit, CD117, MASTC, PBT, SCFR}
- **Diseases:** esophageal or gastric varices (MESH:D004932), bleeding (MESH:D006470), obesity (MESH:D009765), diarrhea (MESH:D003967), proteinuria (MESH:D011507), inflammatory (MESH:D007249), impaired liver function (MESH:D008107), cirrhosis (MESH:D005355), variceal bleeding (MESH:D014648), cirrhotic (MESH:D000094724), Rapidly accelerated fibrosarcoma (MESH:D005354), NAFLD (MESH:D065626), hand-foot skin reaction (MESH:D060831), Cancer (MESH:D009369), type 2 diabetes (MESH:D003924), hepatitis (MESH:D056486), chronic hepatitis B or C (MESH:D019694), liver dysfunction (MESH:D017093), BCLC (MESH:D006528), gastrointestinal bleeding (MESH:D006471), portal hypertension (MESH:D006975), hypertension (MESH:D006973), deaths (MESH:D003643), endocrinopathies (MESH:C567425), toxicities (MESH:D064420), Child-Pugh (MESH:C562515)
- **Chemicals:** aflatoxin (MESH:D000348), cabozantinib (MESH:C558660), atezolizumab (MESH:C000594389), ipilimumab (MESH:D000074324), Sorafenib (MESH:D000077157), bevacizumab (MESH:D000068258), TAM (MESH:D013629), bilirubin (MESH:D001663), steroid (MESH:D013256), Durvalumab (MESH:C000613593), Lenvatinib (MESH:C531958), Nivolumab (MESH:D000077594), alcohol (MESH:D000438), Tremelimumab (MESH:C520704), IMbrave150 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12963680/full.md

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Source: https://tomesphere.com/paper/PMC12963680