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Analysis of a National Programme for Selective Internal Radiation Therapy for Colorectal Cancer Liver Metastases
Authors:J. White  G. Carolan-Rees  M. Dale  H.E. Morgan  H.E. Patrick  T.C. See  E.L. Beeton  D.E.B. Swinson  J.K. Bell  D.M. Manas  A. Crellin  N.J. Slevin  R.A. Sharma
Affiliation:1. Cedar, Cardiff & Vale University Health Board, Cardiff Medicentre, Cardiff, UK;2. Cedar, Cardiff University, Cardiff Medicentre, Cardiff, UK;3. Centre for Health Technology Evaluation, National Institute for Health and Care Excellence, London, UK;4. Cambridge University Hospitals NHS Foundation Trust, Addenbrooke''s Hospital, Cambridge, UK;5. Nottingham University Hospitals NHS Trust, Nottingham, UK;7. Department of Radiology, The Christie NHS Foundation Trust, Manchester, UK;11. The Newcastle upon Tyne Hospitals NHS Foundation Trust, Freeman Hospital, Newcastle upon Tyne, UK;12. NHS England, Institute of Oncology, St James''s University Hospital, Leeds, UK;8. The Christie NHS Foundation Trust, Withington, Manchester, UK;9. NIHR University College London Hospitals Biomedical Research Centre, UCL Cancer Institute, University College London, London, UK
Abstract:

Aims

Patients with chemotherapy-refractory colorectal cancer liver metastases have limited therapeutic options. Selective internal radiation therapy (SIRT) delivers yttrium 90 microspheres as a minimally invasive procedure. This prospective, single-arm, observational, service-evaluation study was part of National Health Service England Commissioning through Evaluation.

Methods

Patients eligible for treatment had histologically confirmed carcinoma with liver-only/liver-dominant metastases with clinical progression during or following oxaliplatin-based and irinotecan-based chemotherapy. All patients received SIRT plus standard of care. The primary outcome was overall survival; secondary outcomes included safety, progression-free survival (PFS) and liver-specific PFS (LPFS).

Results

Between December 2013 and March 2017, 399 patients were treated in 10 centres with a median follow-up of 14.3 months (95% confidence interval 9.2–19.4). The median overall survival was 7.6 months (95% confidence interval 6.9–8.3). The median PFS and LPFS were 3.0 months (95% confidence interval 2.8–3.1) and 3.7 months (95% confidence interval 3.2–4.3), respectively. During the follow-up period, 143 patients experienced an adverse event and 8% of the events were grade 3.

Conclusion

Survival estimates from this pragmatic study show clinical outcomes attainable in the National Health Service comparable with previously published data. This study shows the value of a registry-based commissioning model to aid national commissioning decisions for highly specialist cancer treatments.
Keywords:Brachytherapy  colorectal cancer  commissioning models  liver metastases  molecular radiotherapy  transarterial radio-embolisation
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