22 Quality of life and services use in patients diagnosed with brain tumours: data from a national cancer survivorship study

Abstract Introduction About 13,000 new patients are diagnosed annually with a primary brain tumour in the UK and less than 20% of patients survive 10 years post-diagnosis. Patient-Reported Outcomes and Experiences (PROMs & PREMs) are largely used in clinical trials that recruit fitter and younger patients than patients routinely treated. Indigo is a randomised controlled digital clinical trial aimed at capturing adult cancer patients’ PROMs and PREMs. Methods We have implemented an online, patient-completed, randomised observational trial. We identified all patients who self-reported having a brain tumour and assessed their EQ-5D-5L scores, demographics and socio-economics metrics, and their use of health services. Results Between January 2025 and 1st of February 2026, 67,860 patients provided informed consent and enrolled in the trial, of whom 188 patients (0.3%) had a brain tumour and were eligible for analysis. The median age was 55 years old, 95% were white; 93%, heterosexual and 51%, women. 59% were diagnosed over 5 years ago and the oldest year of diagnosis was late 1980s. 47% patients received surgery, chemoradiotherapy; 45% reported that their tumour was still present and 44% that their tumour was cured. Most patients reported problems with anxiety and depression (62%) and performing their usual activities (61%). Over 60% saw either their GP (69%) or their hospital doctor (62%) and 55% would contact their CNS if they had a concern about their diagnosis. Conclusion This is the first national study to look at quality of life and service use in brain tumour patients. Patients report issues with mental health and activities of daily living, and patients diagnosed over 5 years ago still have annual appointments. We are continuing to recruit to the trial.

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Journal
Neuro-Oncology
Published
2026-08-27
DOI
https://doi.org/10.1093/neuonc/noag172.013
Primary Topic
Mental Health and Patient Involvement
Type
article
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article

22 Quality of life and services use in patients diagnosed with brain tumours: data from a national cancer survivorship study

Kendall Jamieson Gilmore, Laura Ashley, Jacqui Gath, Pete Wheatstone et al.
Neuro-Oncology
Mental Health and Patient Involvement
article

22 Quality of life and services use in patients diagnosed with brain tumours: data from a national cancer survivorship study

Kendall Jamieson Gilmore, Laura Ashley, Jacqui Gath, Pete Wheatstone, Garry Davenport, Lillie Pakzad-Shahabi, Kerlann Le Calvez, Helen Williams, Jonathan Gregory, Katri Langel, Owen Chinembiri, Clara Miglio, Danush Padmasri, Anthony Cunliffe, Matthew Williams, Danny Ruta
article en

Abstract

Abstract Introduction About 13,000 new patients are diagnosed annually with a primary brain tumour in the UK and less than 20% of patients survive 10 years post-diagnosis. Patient-Reported Outcomes and Experiences (PROMs & PREMs) are largely used in clinical trials that recruit fitter and younger patients than patients routinely treated. Indigo is a randomised controlled digital clinical trial aimed at capturing adult cancer patients’ PROMs and PREMs. Methods We have implemented an online, patient-completed, randomised observational trial. We identified all patients who self-reported having a brain tumour and assessed their EQ-5D-5L scores, demographics and socio-economics metrics, and their use of health services. Results Between January 2025 and 1st of February 2026, 67,860 patients provided informed consent and enrolled in the trial, of whom 188 patients (0.3%) had a brain tumour and were eligible for analysis. The median age was 55 years old, 95% were white; 93%, heterosexual and 51%, women. 59% were diagnosed over 5 years ago and the oldest year of diagnosis was late 1980s. 47% patients received surgery, chemoradiotherapy; 45% reported that their tumour was still present and 44% that their tumour was cured. Most patients reported problems with anxiety and depression (62%) and performing their usual activities (61%). Over 60% saw either their GP (69%) or their hospital doctor (62%) and 55% would contact their CNS if they had a concern about their diagnosis. Conclusion This is the first national study to look at quality of life and service use in brain tumour patients. Patients report issues with mental health and activities of daily living, and patients diagnosed over 5 years ago still have annual appointments. We are continuing to recruit to the trial.

Neuro-OncologyVol. 28(Supplement_1)
European Observatory on Health Systems and Policies (BE), Guy's Hospital (GB), University of Leeds (GB), Imperial College Healthcare NHS Trust (GB), Macmillan Cancer Support (GB), Charing Cross Hospital (GB), Cambridge University Hospitals NHS Foundation Trust (GB), Sleep Research Society (US), National Institute for Health and Care Excellence (GB), NIHR Imperial Biomedical Research Centre (GB), NIHR Birmingham Biomedical Research Centre (GB), Imperial College London (GB), University of Worcester (GB), Leeds Beckett University (GB)
Openalex Percentile: Top 6%
Mental Health and Patient Involvement
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