Finbar Slevin
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Finbar Slevin has a total of 235 co-authors. Here are the top co-authors by number of shared publications:
- Ann Henry
Leeds Institute of Medical Research, University of Leeds, Leeds, UK
9 shared publications - Louise Murray
Department of Clinical Oncology, Leeds Cancer Centre, Leeds, UK; Leeds Institute of Medical Research, University of Leeds, Leeds, UK
9 shared publications - John Lilley
Department of Medical Physics, Leeds Teaching Hospitals NHS Trust, Beckett Street, Leeds, LS9 7TF, UK
6 shared publications - Eleanor Mae Hudson
Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK
5 shared publications - Alexandra Smith
Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK
4 shared publications - Sarah Rose Brown
Leeds Cancer Research UK Clinical Trials Unit, Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK
4 shared publications
Latest Publications
- Open Access
- 28 May 2026
- Published by Elsevier in Clinical Oncology
- Vol. 56, 104203
Clinical Oncologist and NHS Commissioner Perspectives on Reirradiation for Recurrent Cancer
- 28 May 2026
- Published by Elsevier in Clinical Oncology
- Vol. 56, 104203
Open AccessClinical Oncologist and NHS Commissioner Perspectives on Reirradiation for Recurrent Cancer
- Open Access
- 28 May 2026
- Published by Elsevier in Clinical Oncology
- Vol. 56, 104201
Patient Perspectives on Reirradiation for Recurrent Cancer, to Inform Future Clinical Trial Design
- 28 May 2026
- Published by Elsevier in Clinical Oncology
- Vol. 56, 104201
Open AccessPatient Perspectives on Reirradiation for Recurrent Cancer, to Inform Future Clinical Trial Design
- Open Access
- 19 February 2026
- Published by Elsevier in Clinical Oncology
- Vol. 52, 104085
Reirradiation Options for Previously Irradiated Prostate Cancer: Is It Feasible to Randomise Between Treatment With Stereotactic Body Radiotherapy (SBRT) Versus High-Dose-Rate Brachytherapy?
- 19 February 2026
- Published by Elsevier in Clinical Oncology
- Vol. 52, 104085
Open AccessReirradiation Options for Previously Irradiated Prostate Cancer: Is It Feasible to Randomise Between Treatment With Stereotactic Body Radiotherapy (SBRT) Versus High-Dose-Rate Brachytherapy?
- Open Access
- 11 September 2025
- Published by Elsevier in Clinical Oncology
- Vol. 47, 103937
Radiating Excellence: A Decade of Pioneering Radiotherapy Trials and Collaborative Leadership at Leeds Cancer Research UK Clinical Trials Unit
- 11 September 2025
- Published by Elsevier in Clinical Oncology
- Vol. 47, 103937
Open AccessRadiating Excellence: A Decade of Pioneering Radiotherapy Trials and Collaborative Leadership at Leeds Cancer Research UK Clinical Trials Unit
- 26 July 2025
- Published by Elsevier in Clinical Oncology
- Vol. 46, 103912
The POINTER-PC Study-determining Optimal Radiotherapy for Pelvic Nodal Recurrence in Prostate Cancer
- 26 July 2025
- Published by Elsevier in Clinical Oncology
- Vol. 46, 103912
The POINTER-PC Study-determining Optimal Radiotherapy for Pelvic Nodal Recurrence in Prostate Cancer
- 3 July 2025
- Published by Elsevier in Clinical Oncology
- Vol. 45, 103901
Response to ‘Dose Accumulation for Pelvic Stereotactic Ablative Radiotherapy Reirradiation. In Regard to Slevin et al.’
- 3 July 2025
- Published by Elsevier in Clinical Oncology
- Vol. 45, 103901
Response to ‘Dose Accumulation for Pelvic Stereotactic Ablative Radiotherapy Reirradiation. In Regard to Slevin et al.’
- Open Access
- 9 May 2025
- Published by Elsevier in Clinical Oncology
- Vol. 43, 103861
Dose Accumulation for Pelvic Stereotactic Ablative Radiotherapy Reirradiation
- 9 May 2025
- Published by Elsevier in Clinical Oncology
- Vol. 43, 103861
Open AccessDose Accumulation for Pelvic Stereotactic Ablative Radiotherapy Reirradiation
- Open Access
Pelvis Or Involved Node Treatment: Eradicating Recurrence in Prostate Cancer (POINTER-PC) – study protocol paper for a phase III multicentre, open-label randomised controlled trial
Introduction Prostate cancer (PCa) is the most common cancer in men. Recurrence may occur in up to half of patients initially treated with curative intent for high-risk localised/locally advanced PCa. Pelvic nodal recurrence is common in this setting, but no clear standard of care exists for these patients, with potential therapeutic approaches including stereotactic body radiotherapy (SBRT) to the involved node(s) alone, extended nodal irradiation (ENI) to treat sites of potential micrometastatic spread in addition to involved node(s) and androgen deprivation therapy with or without additional systemic anticancer therapies. Based on observational studies, ENI is associated with promising metastasis-free survival (MFS) compared with SBRT and appears to result in low rates of severe late toxicity. Methods and analysis Pelvis Or Involved Node Treatment: Eradicating Recurrence in Prostate Cancer is a UK multicentre, open-label, phase III randomised controlled trial, which will deliver much needed, high-quality evidence of the impact on metastatic progression from ENI compared with SBRT in patients with PCa pelvic nodal recurrence. The trial will also evaluate the long-term toxicity of 5-fraction ENI compared with a standard 20-fraction schedule. The trail will randomise 480 participants in a ratio of 2:1:1 to SBRT, 5-fraction ENI or 20-fraction ENI from 35 to 40 UK radiotherapy sites over 4 years. Coprimary endpoints are MFS at 3 years and participant-reported late bowel toxicity at 3 years. Secondary endpoints include overall survival, biochemical progression-free survival, failure-free survival, patterns of failure, participant-reported/clinician-reported toxicity and health-related quality of life. Collection of blood and tissue samples will enable future evaluation of biomarkers of disease and toxicity and support stratification of salvage therapeutic approaches. Ethics and dissemination Ethical approval was obtained from NHS Health Research Authority, East of England – Cambridgeshire and Hertfordshire Research Ethics Committee (24/EE/0099). Trial results will be published in peer-reviewed journals and adhere to International Committee of Medical Journal Editors guidelines. Trial registration number ISRCTN11089334, registered on 23 September 2024.
Open AccessPelvis Or Involved Node Treatment: Eradicating Recurrence in Prostate Cancer (POINTER-PC) – study protocol paper for a phase III multicentre, open-label randomised controlled trial
Introduction Prostate cancer (PCa) is the most common cancer in men. Recurrence may occur in up to half of patients initially treated with curative intent for high-risk localised/locally advanced PCa. Pelvic nodal recurrence is common in this setting, but no clear standard of care exists for these patients, with potential therapeutic approaches including stereotactic body radiotherapy (SBRT) to the involved node(s) alone, extended nodal irradiation (ENI) to treat sites of potential micrometastatic spread in addition to involved node(s) and androgen deprivation therapy with or without additional systemic anticancer therapies. Based on observational studies, ENI is associated with promising metastasis-free survival (MFS) compared with SBRT and appears to result in low rates of severe late toxicity. Methods and analysis Pelvis Or Involved Node Treatment: Eradicating Recurrence in Prostate Cancer is a UK multicentre, open-label, phase III randomised controlled trial, which will deliver much needed, high-quality evidence of the impact on metastatic progression from ENI compared with SBRT in patients with PCa pelvic nodal recurrence. The trial will also evaluate the long-term toxicity of 5-fraction ENI compared with a standard 20-fraction schedule. The trail will randomise 480 participants in a ratio of 2:1:1 to SBRT, 5-fraction ENI or 20-fraction ENI from 35 to 40 UK radiotherapy sites over 4 years. Coprimary endpoints are MFS at 3 years and participant-reported late bowel toxicity at 3 years. Secondary endpoints include overall survival, biochemical progression-free survival, failure-free survival, patterns of failure, participant-reported/clinician-reported toxicity and health-related quality of life. Collection of blood and tissue samples will enable future evaluation of biomarkers of disease and toxicity and support stratification of salvage therapeutic approaches. Ethics and dissemination Ethical approval was obtained from NHS Health Research Authority, East of England – Cambridgeshire and Hertfordshire Research Ethics Committee (24/EE/0099). Trial results will be published in peer-reviewed journals and adhere to International Committee of Medical Journal Editors guidelines. Trial registration number ISRCTN11089334, registered on 23 September 2024.
- Open Access
- 17 December 2024
- Published by Elsevier in Clinical Oncology
- Vol. 39, 103732
Best Practice for Patient-centred Radiotherapy in Clinical Trials and Beyond—A National Multidisciplinary Consensus
- 17 December 2024
- Published by Elsevier in Clinical Oncology
- Vol. 39, 103732
Open AccessBest Practice for Patient-centred Radiotherapy in Clinical Trials and Beyond—A National Multidisciplinary Consensus
- 15 May 2024
- Published by Elsevier in Clinical Oncology
- Vol. 36 (9) , 537-540
Radiology Training for Clinical Oncology Trainees
- 15 May 2024
- Published by Elsevier in Clinical Oncology
- Vol. 36 (9) , 537-540
Radiology Training for Clinical Oncology Trainees