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Efficacy and safety of autologous haematopoietic stem cell transplantation versus alemtuzumab, ocrelizumab, ofatumumab or cladribine in relapsing remitting multiple sclerosis (StarMS): protocol for a randomised controlled trial
Brittain, Gavin ; Petrie, Jennifer ; Duffy, Kate ; Glover, Rachel ; Hullock, Katie ; Papaioannou, Diana ; Roldan, Elisa ; Beecher, Colette ; Bursnall, Matthew ; Ciccarelli, Olga ... show 10 more
Brittain, Gavin
Petrie, Jennifer
Duffy, Kate
Glover, Rachel
Hullock, Katie
Papaioannou, Diana
Roldan, Elisa
Beecher, Colette
Bursnall, Matthew
Ciccarelli, Olga
Gloucestershire Author
Date
2024-02-05
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Abstract
Introduction: Autologous haematopoietic stem cell transplantation (aHSCT) is increasingly used as treatment for patients with active multiple sclerosis (MS), typically after failure of disease-modifying therapies (DMTs). A recent phase III trial, 'Multiple Sclerosis International Stem Cell Transplant, MIST', showed that aHSCT resulted in prolonged time to disability progression compared with DMTs in patients with relapsing remitting MS (RRMS). However, the MIST trial did not include many of the current high-efficacy DMTs (alemtuzumab, ocrelizumab, ofatumumab or cladribine) in use in the UK within the control arm, which are now offered to patients with rapidly evolving severe MS (RES-MS) who are treatment naïve. There remain, therefore, unanswered questions about the relative efficacy and safety of aHSCT over these high-efficacy DMTs in these patient groups. The StarMS trial (Autologous Stem Cell Transplantation versus Alemtuzumab, Ocrelizumab, Ofatumumab or Cladribine in Relapsing Remitting Multiple Sclerosis) will assess the efficacy, safety and long-term impact of aHSCT compared with high-efficacy DMTs in patients with highly active RRMS despite the use of standard DMTs or in patients with treatment naïve RES-MS.
Methods and analysis: StarMS is a multicentre parallel-group rater-blinded randomised controlled trial with two arms. A total of 198 participants will be recruited from 19 regional neurology secondary care centres in the UK. Participants will be randomly allocated to the aHSCT arm or DMT arm in a 1:1 ratio. Participants will remain in the study for 2 years with follow-up visits at 3, 6, 9, 12, 18 and 24 months postrandomisation. The primary outcome is the proportion of patients who achieve 'no evidence of disease activity' during the 2-year postrandomisation follow-up period in an intention to treat analysis. Secondary outcomes include efficacy, safety, cost-effectiveness and immune reconstitution of aHSCT and the four high-efficacy DMTs.
Citation
Brittain, G., Petrie, J., Duffy, K. E. M., Glover, R., Hullock, K., Papaioannou, D., Roldan, E., Beecher, C., Bursnall, M., Ciccarelli, O., Coles, A. J., Cooper, C., Giovannoni, G., Gabriel, I., Kazmi, M., Kyriakou, C., Nicholas, R., Paling, D., Peniket, A., Scolding, N., … StarMS trial team (2024). Efficacy and safety of autologous haematopoietic stem cell transplantation versus alemtuzumab, ocrelizumab, ofatumumab or cladribine in relapsing remitting multiple sclerosis (StarMS): protocol for a randomised controlled trial. BMJ open, 14(2), e083582. https://doi.org/10.1136/bmjopen-2023-083582
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