ReviewNanomedicine (London, England)2026
Advancing prussian blue nanoparticle-mediated photothermal therapy through machine learning and multiomics integration.
Review in Nanomedicine (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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
1 citing paper in PubMed.
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
Abstract
Prussian blue nanoparticles (PBNPs) are a versatile platform for administering photothermal therapy (PTT) in cancer therapy applications. PBNPs combine biocompatibility, safety, and clinical translational potential with durable treatment outcomes in preclinical cancer models. In this perspective, we focus on aspects critical to the workflow of implementing PBNP-PTT in cancer treatment, drawing inspiration from adjacent scientific areas that have not been described in the context of PBNPs, but are important for improving the delivery of PBNP-PTT and its translation. Specifically, we will discuss machine learning approaches, multiomics analyses, and clinical strategies pertinent to PBNP-PTT. Machine learning approaches have the potential to enhance PBNP-PTT design, performance, and therapeutic outcomes. Complementing this, multiomics has the potential to describe the responses to PBNP-PTT, particularly its immune effects. By embedding these advances from nanoparticle engineering to therapy monitoring, PBNP-PTT can evolve from empirical tumor ablation toward a precision photothermal platform, enabling highly individualized cancer treatments with improved safety, efficacy, regulatory approval, and clinical predictability. We will also cover clinical strategies pertinent to the translation PBNP-PTT culminating with specific forward-looking perspectives. This convergence of nanotechnology, immunology, and data science positions PBNP-PTT at the forefront of next-generation cancer nanomedicine and immunotherapy.
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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 OpenQuestion graph.