Inclusive Trial Designs in Acute Spinal Cord Injuries: Prediction–Based Stratification of Clinical Walking Outcome and Projected Enrolment Frequencies

Author:

Cathomen Adrian123ORCID,Sirucek Laura345,Killeen Tim1,Abel Rainer67,Maier Doris78,Weidner Norbert79,Rupp Rüdiger79,Hothorn Torsten10,Steeves John D.11,Curt Armin137,Bolliger Marc137ORCID

Affiliation:

1. Spinal Cord Injury Center, Balgrist University Hospital, Zurich, Switzerland

2. ETH Zurich, Zurich, Switzerland

3. Neuroscience Center Zurich, University of Zurich, Zurich, Switzerland

4. Integrative Spinal Research, Department of Chiropractic Medicine, Balgrist University Hospital, University of Zurich, Zurich, Switzerland

5. University of Zurich, Zurich, Switzerland

6. Trauma Center Bayreuth, Bayreuth, Germany

7. EMSCI Study Group

8. Trauma Center Murnau, Murnau, Germany

9. Spinal Cord Injury Center, Heidelberg University Hospital, Heidelberg, Germany

10. Epidemiology, Biostatistics and Prevention Institute, University of Zurich, Zurich, Switzerland

11. ICORD, Blusson Spinal Cord Centre, University of British Columbia and Vancouver Coastal Health, Vancouver, BC, Canada

Abstract

Background New therapeutic approaches in neurological disorders are progressing into clinical development. Past failures in translational research have underlined the critical importance of selecting appropriate inclusion criteria and primary outcomes. Narrow inclusion criteria provide sensitivity, but increase trial duration and cost to the point of infeasibility, while broader requirements amplify confounding, increasing the risk of trial failure. This dilemma is perhaps most pronounced in spinal cord injury (SCI), but applies to all neurological disorders with low frequency and/or heterogeneous clinical manifestations. Objective Stratification of homogeneous patient cohorts to enable the design of clinical trials with broad inclusion criteria. Methods Prospectively–gathered data from patients with acute cervical SCI were analysed using an unbiased recursive partitioning conditional inference tree (URP–CTREE) approach. Performance in the 6-minute walk test at 6 months after injury was classified based on standardized neurological assessments within the first 15 days of injury. Functional and neurological outcomes were tracked throughout rehabilitation up to 6 months after injury. Results URP–CTREE identified homogeneous outcome cohorts in a study group of 309 SCI patients. These cohorts were validated by an internal, yet independent, validation group of 172 patients. The study group cohorts identified demonstrated distinct recovery profiles throughout rehabilitation. The baseline characteristics of the analysed groups were compared to a reference group of 477 patients. Conclusion URP–CTREE enables inclusive trial design by revealing the distribution of outcome cohorts, discerning distinct recovery profiles and projecting potential patient enrolment by providing estimates of the relative frequencies of cohorts to improve the design of clinical trials in SCI and beyond.

Funder

International Foundation for Research in Paraplegia

European Union’s Horizon 2020 research and innovation programme

Publisher

SAGE Publications

Subject

General Medicine

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