Endocrine and multiple sclerosis outcomes in patients with autoimmune thyroid events in the alemtuzumab CARE-MS studies

Author:

Dayan Colin M.1ORCID,Lecumberri Beatriz2,Muller Ilaria3ORCID,Ganesananthan Sashiananthan1,Hunter Samuel F.4,Selmaj Krzysztof W.5,Hartung Hans-Peter6,Havrdova Eva K.7,LaGanke Christopher C.8,Ziemssen Tjalf9ORCID,Van Wijmeersch Bart10,Meuth Sven G.11,Margolin David H.12,Poole Elizabeth M.12,Baker Darren P.12,Senior Peter A.13

Affiliation:

1. Cardiff University School of Medicine, Cardiff, UK

2. La Paz University Hospital, Universidad Autónoma de Madrid, Madrid, Spain

3. Cardiff University School of Medicine, Cardiff, UK Fondazione IRCCS Ca’ Granda Ospedale Policlinico Maggiore, Milan, Italy University of Milan, Milan, Italy

4. Advanced Neurosciences Institute, Franklin, TN, USA

5. Department of Neurology, University of Warmia and Mazury, Olsztyn, Poland

6. Department of Neurology, Medical Faculty, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany Brain and Mind Centre, University of Sydney, Sydney, Australia Department of Neurology, Medical University of Vienna, Vienna, Austria Department of Neurology, Palacky University Olomouc, Olomouc, Czech Republic

7. First Medical Faculty, Department of Neurology, Charles University, Prague, Czech Republic

8. North Central Neurology Associates, Cullman, AL, USA

9. Center of Clinical Neuroscience, Carl Gustav Carus University Hospital, Dresden, Germany

10. Universitair MS Centrum, Hasselt-Pelt, Belgium

11. Department of Neurology, Medical Faculty, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany

12. Sanofi, Cambridge, MA, USA

13. University of Alberta, Edmonton, Alberta, Canada

Abstract

Background Alemtuzumab is an effective therapy for relapsing multiple sclerosis. Autoimmune thyroid events are a common adverse event. Objective Describe endocrine and multiple sclerosis outcomes over 6 years for alemtuzumab-treated relapsing multiple sclerosis patients in the phase 3 CARE-MS I, II, and extension studies who experienced adverse thyroid events. Methods Endocrine and multiple sclerosis outcomes were evaluated over 6 years. Thyroid event cases, excluding those pre-existing or occurring after Year 6, were adjudicated retrospectively by expert endocrinologists independently of the sponsor and investigators. Results Thyroid events were reported for 378/811 (46.6%) alemtuzumab-treated patients. Following adjudication, endocrinologists reached consensus on 286 cases (75.7%). Of these, 39.5% were adjudicated to Graves’ disease, 2.5% Hashimoto's disease switching to hyperthyroidism, 15.4% Hashimoto's disease, 4.9% Graves’ disease switching to hypothyroidism, 10.1% transient thyroiditis, and 27.6% with uncertain diagnosis; inclusion of anti-thyroid antibody status reduced the number of uncertain diagnoses. Multiple sclerosis outcomes of those with and without thyroid events were similar. Conclusion Adjudicated thyroid events occurring over 6 years for alemtuzumab-treated relapsing multiple sclerosis patients were primarily autoimmune. Thyroid events were considered manageable and did not affect disease course. Thyroid autoimmunity is a common but manageable adverse event in alemtuzumab-treated relapsing multiple sclerosis patients. ClinicalTrials.gov Registration Numbers: CARE-MS I (NCT00530348); CARE-MS II (NCT00548405); CARE-MS Extension (NCT00930553)

Funder

Bayer Healthcare Pharmaceuticals

Sanofi

Publisher

SAGE Publications

Subject

Cellular and Molecular Neuroscience,Neurology (clinical)

Reference39 articles.

1. Genzyme Corporation LEMTRADA (alemtuzumab). https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/103948s5158lbl.pdf. Accessed 8 January 2020.

2. Sanofi Belgium LEMTRADA summary of product characteristics. Accessed 8 January 2020.

3. Alemtuzumab versus interferon beta 1a as first-line treatment for patients with relapsing-remitting multiple sclerosis: a randomised controlled phase 3 trial

4. Alemtuzumab CARE-MS II 5-year follow-up

5. Alemtuzumab for patients with relapsing multiple sclerosis after disease-modifying therapy: a randomised controlled phase 3 trial

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