ReviewJournal of hepatocellular carcinoma2026
Intratumoral Tertiary Lymphoid Structures in Hepatocellular Carcinoma: Current Evidence and Future Directions - a Narrative Review.
Review in Journal of hepatocellular carcinoma, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Intratumoral tertiary lymphoid structures (iTLSs) have emerged as critical immune features in hepatocellular carcinoma (HCC). This narrative review critically synthesizes current evidence (sourced from PubMed, Embase, and Web of Science up to January 2026) on the biological mechanisms, pathological assessment, non-invasive imaging, and clinical implications of iTLSs. Moving beyond simple binary classifications, we emphasize that precise scoring based on morphological maturation is essential. Clinically, functionally mature iTLSs are strongly associated with favorable prognosis and immunotherapy benefits, though metabolic etiologies (e.g, NASH) can drive complex immunosuppression. Furthermore, while non-invasive radiomic models show high predictive accuracy, their clinical translation is hindered by mathematical overfitting and a "black box" lack of biological interpretability. Translating these biological insights into clinical practice, particularly through non-invasive imaging biomarkers and standardized pathological evaluations, holds great promise for guiding personalized immunotherapy. Ultimately, however, overcoming inter-study heterogeneity and conducting rigorous functional validations remain imperative before their routine clinical integration.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.