ReviewFrontiers in oncology2026
AI-enabled precision prediction and proactive management of cutaneous toxicities in cancer immunoradiotherapy (ICI+RT).
Review in Frontiers in oncology, 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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Immunoradiotherapy has become an increasingly important strategy for the treatment of advanced malignant tumors, but its broader application is accompanied by a high incidence of cutaneous toxicities, including radiation dermatitis and immune-related skin adverse events. These toxicities often emerge early during treatment, exhibit substantial inter-patient heterogeneity, and can compromise treatment continuity and patient quality of life. Conventional management remains largely reactive and grading-based, offering limited capacity for individualized risk assessment or early intervention. Recent advances highlight that cutaneous toxicity in immunoradiotherapy arises from the convergence of radiation-induced tissue injury and immune checkpoint blockade-driven immune amplification, involving interconnected pathways such as DNA damage-associated danger signaling, innate immune activation, cytokine amplification, and dysregulated T-cell effector responses. This biological complexity limits the predictive utility of single-factor or mechanism-isolated approaches, underscoring the need for integrative, data-driven strategies. In this mini-review, we synthesize emerging AI-enabled approaches for precision prediction and management of cutaneous toxicities in immunoradiotherapy. We focus on how clinicodosimetric variables, spatial dose topology, imaging- and radiomics-derived tissue susceptibility, and accessible immune-inflammatory surrogates can be integrated into pathway-informed predictive models. We further discuss translational frameworks that embed prediction into clinical workflows, enabling plan-aware exposure mitigation, proactive supportive care stratification, and dynamic on-treatment risk updating. Collectively, these advances position cutaneous toxicity as a tractable and clinically meaningful endpoint for precision management in immunoradiotherapy, aligned with the goals of data-driven oncology.
Indexed as
Identifiers
What OpenQuestion holds
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 OpenQuestion graph.