Evidence map›Paper›PMID 41748196›Full record

ArticleBMJ open2026

Protocol of the RADIO-STAR trial: a phase 1 safety and dose finding study of hypofractionated radiotherapy to the stellate ganglia for the treatment of ventricular arrhythmia.

Benjamin Mothibe Bussmann, Ben George, Maxwell Robinson, James Grist, Prabakar Sukumar, Ebison Chinherende, Fintan Sheerin, Veni Enzhil, Oliver Rider, Bleddyn Jones and 2 more

Abstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Benjamin Mothibe BussmannDepartment of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0003-3343-2590
Ben GeorgeGenesisCare UK, Oxford, UK.
Maxwell RobinsonDepartment of Radiotherapy Physics, Oxford University Hospitals NHS Foundation Trust, Oxford, England, UK.
James GristOxford Centre for Clinical Magnetic Resonance Research, University of Oxford, Oxford, England, UK.
Prabakar SukumarDepartment of Radiology, Oxford University Hospitals NHS Foundation Trust, Oxford, England, UK.
Ebison ChinherendeGenesisCare UK, Oxford, UK.
Fintan SheerinGenesisCare UK, Oxford, UK.
Veni EnzhilGenesisCare UK, Oxford, UK.
Oliver RiderOxford Centre for Clinical Magnetic Resonance Research, University of Oxford, Oxford, England, UK.
Bleddyn JonesDepartment of Oncology, Oxford University Hospitals NHS Foundation Trust, Oxford, England, UK.
Ami SabharwalGenesisCare UK, Oxford, UK.
Neil HerringDepartment of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK neil.herring@dpag.ox.ac.uk.ORCID http://orcid.org/0000-0001-8453-6133

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSympathetic activation is the hallmark of cardiac disease, driving disease progression and triggering ventricular arrhythmia (VA). Despite optimal medical therapy, many patients experience recurrent VAs refractory to medical therapy, leading to repetitive implantable cardioverter defibrillator (ICD) therapy, worse quality of life and adverse outcomes. Cardiac sympathetic denervation (CSD) through surgical removal of the stellate ganglia is an effective treatment for refractory VAs but carries a high complication rate. We hypothesise that high precision image guided radiotherapy can be used to target the stellate ganglia to achieve CSD non-invasively. METHODS AND ANALYSIS: RADIO-STAR (hypofractionated radiotherapy to the stellate ganglia for ventricular arrhythmia) is a first-in-human, phase 1 safety and dose finding study of radiotherapy to the stellate ganglia in patients with recurrent VAs. Patients with structural heart disease requiring recurrent ICD therapy for VAs are invited to undergo radiotherapy bilaterally to their stellate ganglia with a predetermined sample size of n=13. Radiotherapy dose will be determined by a prespecified dose escalation protocol. The primary outcome is safety defined as any treatment-related grade 3-5 toxicity occurring within 6 months of radiotherapy treatment, as defined by the Common Terminology Criteria for Adverse Events or any treatment-related side effects detected on patient symptom questionnaires and clinical examination during study visits. Secondary outcome measures to evaluate feasibility and efficacy include ability to safely deliver radiotherapy and consequent changes in circulating catecholamines and neuropeptide-Y, heart rate variability, structural changes in the stellate ganglia on MRI imaging and ICD therapy burden. ETHICS AND DISSEMINATION: This study has received ethical approval by the South Central-Oxford B Research Ethics Committee (REC/SC/0005). Study findings will be submitted for publication in peer-reviewed scientific journals and presented at national and/or international scientific conferences. TRIAL REGISTRATION NUMBER: ISRCTN49861434.

Indexed as

Arrhythmias, CardiacRadiation Dose HypofractionationRadiotherapy, Image-GuidedStellate GanglionClinical Trials, Phase I as TopicDefibrillators, ImplantableFemaleHumansQuality of LifeSympathectomyTreatment OutcomeAdult radiotherapyCardiomyopathyPacing & electrophysiology

Identifiers

PMID41748196
PMCPMC12959014

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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.