Real-world effectiveness of cladribine for Australian patients with multiple sclerosis: An MSBase registry substudy

Author:

Lizak Nathaniel1,Hodgkinson Suzanne2,Butler Ernest3,Lechner-Scott Jeannette4,Slee Mark5,McCombe Pamela Ann6,Shaw Cameron7,Skibina Olga8,Vucic Steve9,Shuey Neil10,Barnett Michael H11,Parratt John12,Butzkueven Helmut13,Jack Dominic14,Fabris Jessica15,Kalincik Tomas16

Affiliation:

1. CORe, Department of Medicine, University of Melbourne, Melbourne, VIC, Australia/The Alfred Hospital, Melbourne, VIC, Australia

2. Ingham Institute for Applied Medical Research, UNSW Medicine, Liverpool, NSW, Australia/Liverpool Hospital, Sydney, NSW, Australia

3. Monash Medical Centre, Monash University, Melbourne, VIC, Australia

4. Hunter New England Health and Hunter Medical Research Institute, University of Newcastle, Callaghan, NSW, Australia

5. Flinders University, Adelaide, SA, Australia

6. Royal Brisbane and Women’s Hospital, University of Queensland, Brisbane, QLD, Australia

7. Geelong Hospital, Geelong, VIC, Australia/Deakin University, Melbourne, VIC, Australia

8. The Alfred Hospital, Melbourne, VIC, Australia

9. Westmead Hospital, Sydney, NSW, Australia

10. St Vincent’s Hospital, Melbourne, VIC, Australia

11. Brain and Mind Centre, Sydney, NSW, Australia

12. Royal North Shore Hospital, Sydney, NSW, Australia

13. Central Clinical School, Monash University, Melbourne, VIC, Australia/Eastern Hospital, Melbourne, VIC, Australia

14. Merck KGaA, Darmstadt, Germany

15. Merck Serono Australia Pty Ltd, Frenchs Forest, NSW, Australia

16. CORe, Department of Medicine, University of Melbourne, Melbourne, VIC, Australia/Department of Neurology, Royal Melbourne Hospital, Melbourne, VIC, Australia

Abstract

Background/objective: Observational clinical data from cladribine-treated patients with relapsing forms of multiple sclerosis (MS) were recorded in the Australian MS registry powered by the MSBase registry platform (5-year follow-up) and analysed to complement information from the pivotal cladribine clinical trials in MS. Methods: A cohort of 90 cladribine-treated patients with follow-up data reported by treating physicians and recorded in the Australian MSBase registry (database lock February 2016) were examined. Clinical data included Expanded Disability Status Scale (EDSS) scores, relapses and other disease-modifying drugs (DMDs) administered before and after cladribine treatment. Results: Mean age on starting cladribine was 47 years; mean age at MS onset was 34 years, and median baseline EDSS score was 5.25. Disability trajectories in patients with sufficient follow-up suggested an overall increasing trend prior to cladribine treatment which was reduced during the 2-year post-treatment. Approximately 80% of patients were EDSS progression-free, 65% remained relapse-free after 2 years and median time to next DMD was 1.7 years. Conclusion: These observational data suggest a disease-modifying effect in this cohort of relapsing MS patients characterised by older and more disabled patients. Since these data represent a single-arm cohort, clinical trials and larger comparative post-marketing studies are needed to validate and extend these findings.

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology

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