Outcomes of patients treated in the UK Proton Overseas Programme: non-central nervous system group
Authors
Hwang, E JGaito, Simona
France, Anna
Crellin, A M
Thwaites, D. I.
Ahern, V.
Indelicato, D.
Timmermann, B.
Smith, Ed
Affiliation
The Christie Proton Beam Therapy Centre, The Christie NHS Foundation Trust, Manchester, UKIssue Date
2023
Metadata
Show full item recordAbstract
Aims: The UK Proton Overseas Programme (POP) was launched in 2008. The Proton Clinical Outcomes Unit (PCOU) warehouses a centralised registry for collection, curation and analysis of all outcomes data for all National Health Service-funded UK patients referred and treated abroad with proton beam therapy (PBT) via the POP. Outcomes are reported and analysed here for patients diagnosed with non-central nervous system tumours treated from 2008 to September 2020 via the POP. Materials and methods: All non-central nervous system tumour files for treatments as of 30 September 2020 were interrogated for follow-up information, and type (following CTCAE v4) and time of onset of any late (>90 days post-PBT completion) grade 3-5 toxicities. Results: Four hundred and ninety-five patients were analysed. The median follow-up was 2.1 years (0-9.3 years). The median age was 11 years (0-69 years). 70.3% of patients were paediatric (<16 years). Rhabdomyosarcoma (RMS) and Ewing sarcoma were the most common diagnoses (42.6% and 34.1%). 51.3% of treated patients were for head and neck (H&N) tumours. At last known follow-up, 86.1% of all patients were alive, with a 2-year survival rate of 88.3% and 2-year local control of 90.3%. Mortality and local control were worse for adults (≥25 years) than for the younger groups. The grade 3 toxicity rate was 12.6%, with a median onset of 2.3 years. Most were in the H&N region in paediatric patients with RMS. Cataracts (30.5%) were the most common, then musculoskeletal deformity (10.1%) and premature menopause (10.1%). Three paediatric patients (1-3 years at treatment) experienced secondary malignancy. Seven grade 4 toxicities occurred (1.6%), all in the H&N region and most in paediatric patients with RMS. Six related to eyes (cataracts, retinopathy, scleral disorder) or ears (hearing impairment). Conclusions: This study is the largest to date for RMS and Ewing sarcoma, undergoing multimodality therapy including PBT. It demonstrates good local control, survival and acceptable toxicity rates.Citation
Hwang E, Gaito S, France A, Crellin AM, Thwaites DI, Ahern V, et al. Outcomes of Patients Treated in the UK Proton Overseas Programme: Non-central Nervous System Group. Clinical oncology (Royal College of Radiologists (Great Britain)). 2023 Feb 16. PubMed PMID: 36813694. Epub 2023/02/23. eng.Journal
Clinical OncologyDOI
10.1016/j.clon.2023.02.009PubMed ID
36813694Additional Links
https://dx.doi.org/10.1016/j.clon.2023.02.009Type
ArticleLanguage
enae974a485f413a2113503eed53cd6c53
10.1016/j.clon.2023.02.009