Medical management and intervention (using neurosurgical resection or stereotactic radiosurgery) versus medical management alone for symptomatic brain cavernoma: the CARE pilot RCT

Al-Shahi Salman R, Kitchen N, Forsyth L, Ganesan V, Hall PS, Harkness K, Hutchinson PJ, Lewis SC, Radatz MW, Turner C, Wade J, White DC, White PM
Record ID 32018014471
English
Authors' objectives: The top priority for research into symptomatic cerebral cavernous malformation (also known as brain cavernoma) is whether to have medical management and intervention (using neurosurgical resection or stereotactic radiosurgery) or medical management alone. The primary objective was to assess the feasibility of performing a definitive randomised trial addressing this top priority. The secondary objectives were to set up a collaboration involving patient advocacy organisations and clinicians in the United Kingdom and Ireland; perform a QuinteT Recruitment Intervention to identify facilitators and address barriers to recruitment; and conduct a pilot randomised trial with ≈60 participants.
Authors' results and conclusions: Investigators screened 511 patients at 28/40 (70%) sites in the United Kingdom: 322 (63%) eligible, 202 (63%) approached, 96 (48%) uncertain about whether to have intervention and 72 participants [median age was 51 years (interquartile range 39–59), 41 (57%) female, 66 (92%) white, 56 (78%) with prior intracranial haemorrhage and 28 (39%) with prior epileptic seizure] were randomly assigned to medical management and intervention (n = 36; 12 to neurosurgical resection and 24 to stereotactic radiosurgery) or medical management alone (n = 36) after a recruitment extension. Sixty-seven participants completed follow-up (retention 93%), and adherence was 91%. Barriers to recruitment included usual-care practices and logistical issues with stereotactic radiosurgery, whereas facilitators were neurosurgeons’ preparedness to offer intervention to more people than in usual care, multidisciplinary team equipoise and presenting the study as a solution to equipoise. The primary clinical outcome occurred in 2/33 assigned to medical management and intervention and 2/34 assigned to medical management alone. There were no deaths or serious adverse events. This pilot randomised trial identified facilitators and barriers to recruitment, exceeded its recruitment target and met some feasibility metrics.
Authors' methods: Prospective, randomised, open-label, assessor-blinded, parallel-group trial. A mixed-methods QuinteT Recruitment Intervention analysed sites’ screening logs and qualitative data from audio-recorded recruitment discussions, interviews with healthcare professionals and patients, investigator workshops and observation of meetings. Neuroscience hospitals in the United Kingdom and Ireland. We aimed to recruit ≈60 people of any age, gender and ethnicity who had mental capacity, resided in the United Kingdom/Ireland, and had a brain cavernoma that had caused symptoms due to intracranial haemorrhage, non-haemorrhagic progressive/persistent focal neurological deficit or epileptic seizure(s). We identified and addressed barriers and facilitators to optimise informed consent and recruitment. Computerised, web-based randomisation assigned participants (1 : 1) to treatment of their symptomatic brain cavernoma with medical management and intervention (using neurosurgical resection or stereotactic radiosurgery) or medical management alone. Assignment was open to investigators, participants and carers but not clinical outcome event adjudicators. Feasibility outcomes included site engagement, recruitment, choice of surgical management, retention, adherence, data quality, clinical outcome event rate and protocol implementation. The primary clinical outcome was symptomatic intracranial haemorrhage or new persistent/progressive non-haemorrhagic focal neurological deficit due to brain cavernoma or intervention during ≥ 6 months of follow-up. We could not activate sites in Ireland. The generalisability of our findings outside the United Kingdom is unknown.
Details
Project Status: Completed
Year Published: 2025
URL for additional information: English
English language abstract: An English language summary is available
Publication Type: Full HTA
Country: England, United Kingdom
MeSH Terms
  • Cerebrovascular Disorders
  • Neurosurgery
  • Radiosurgery
  • Intracranial Arteriovenous Malformations
  • Hemangioma, Cavernous, Central Nervous System
Contact
Organisation Name: NIHR Health Technology Assessment programme
Contact Address: NIHR Journals Library, National Institute for Health and Care Research, Evaluation, Trials and Studies Coordinating Centre, Alpha House, University of Southampton Science Park, Southampton SO16 7NS, UK
Contact Name: journals.library@nihr.ac.uk
Contact Email: journals.library@nihr.ac.uk
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