Contributions
Abstract: EP1689
Type: ePoster
Abstract Category: Therapy - disease modifying - 28 Long-term treatment monitoring
Background: Alemtuzumab (ALZ) is a modulatory drug for patients with relapsing-remitting multiple sclerosis (RRMS). Post-marketing surveillance is important to assess the long term safety and effectiveness in a real-world setting. ALZ has therefore been included into the Swedish post-market surveillance study “Immunomodulation and Multiple Sclerosis Epidemiology Study” upon launch in Sweden (March 2014).
Objective: To follow up the effectiveness and long-term safety of ALZ in a real-world setting.
Methods: Swedish MS patients are registered into the nationwide web-based Swedish neuro registry (neuroreg). Before ALZ initiation, patients are asked to participate in the IMSE 3 study. Adverse events (AEs) and clinical measures; extended disability status scale (EDSS), multiple sclerosis severity scale (MSSS), symbol digit modalities test (SDMT), multiple sclerosis impact scale (MSIS-29), European quality of life - 5 dimension test (EQ-5D), are obtained from neuroreg. The Wilcoxon signed-rank test was used to assess changes in effectiveness.
Results: Between March 2014 and April 2017, 104 patients (63% female; 95% RRMS) were included in the IMSE 3 study. Mean age at treatment start was 34 years. Mean number of drugs used before ALZ was 2.8 and most patients switched from Natalizumab (NTZ) (39%). In patients treated with Fingolimod (FGL) before ALZ (n=15), 47% were temporarily (≤ 5 months) treated with NTZ between FGL and ALZ start. 15% had ALZ as their very first disease modifying treatment. Six patients had discontinued ALZ treatment, of which five patients switched to another disease modifying therapy, and one patient died in association with the first ALZ treatment cycle due to fulminant viral hepatitis (Cytomegalovirus, Epstein-Barr Virus). 17 AEs were reported to the Swedish Medical Products Agency, 12 events were classified as non-serious. 97 patients had been treated for at least 12 months and 87 patients for at least 24 months. In patients treated at least 12 months significant improvements were seen for EDSS (2.10±1.57 - 1.67±1.54, n=55), MSSS (3.43±2.76 - 2.64±2.42, n=47), VAS (66.8±21.9 - 73.2±17.7, n=63) and EQ5D (0.67±0.30 - 0.76±0.25, n=70). Conclusions: Neuroreg proves to function well as a post-marketing drug surveillance platform, providing data regarding drug effectiveness and AEs. A longer follow-up period is needed to assess the real-world effectiveness and safety of ALZ.
Disclosure: The IMSE 3 study has received unrestricted grants from Sanofi Genzyme.
Åsa Leandersson has nothing to disclose.
Stina Kågström has nothing to disclose.
Linda Forsberg has nothing to disclose.
Jan Hillert has received honoraria for serving on advisory boards for Biogen, Sanofi-Genzyme and Novartis and speaker's fees from Biogen, Novartis, Merck-Serono, Bayer-Schering, Teva and Sanofi-Genzyme. He has served as P.I. for projects, or received unrestricted research support from, BiogenIdec, Merck-Serono, TEVA, Sanofi-Genzyme and Bayer-Schering.His MS research is funded by the Swedish Research Council and the Swedish Brain foundation.
Petra Nilsson has received travel support from Bayer Schering Pharma, Merck Serono, Biogen and Sanofi Genzyme, honoraria for lectures and advisory boards from Merck Serono and Sanofi Genzyme, advisory boards for Novartis and Roche, lectures for Biogen and has received unrestricted grants from Biogen.
Charlotte Dahle has received unrestricted research grants or honoraria for lectures or advisory boards from Biogen, Novartis, Merck Serono, Teva and Sanofi Genzyme.
Anders Svenningsson has nothing to disclose.
Jan Lycke has received travel support and/or lecture honoraria from Bayer Schering Pharma, Biogen, Novartis, Teva and Sanofi Genzyme; has served on scientific advisory boards for Almirall, Teva, Biogen, Novartis and Sanofi Genzyme; serves on the editorial board of the Acta Neurologica Scandinavica; has received unconditional research grants from Biogen, Novartis and Teva.
Anne-Marie Landtblom has received honoraria from Merck Serono, Teva, Biogen Sanofi Genzyme.
Joachim Burman has received travel support and/or lecture honoraria from Almirall, Biogen, Sanofi Genzyme, Hospira and Merck Serono; has received unconditional research grants from Biogen and Merck Serono.
Fredrik Walentin has received research grants from Biogen and Merck Serono.
Claes Martin has received honoraria for lectures and advisory boards from Merck Serono and Sanofi Genzyme.
Fredrik Piehl has received unrestricted academic research grants from Biogen, Genzyme and Novartis, and travel support and/or compensation for lectures and/or participation in advisory boards from Biogen, Merck Serono, Novartis, Sanofi Genzyme and Teva, which have been exclusively used for the support of research activities.
Tomas Olsson has received unrestricted research grants or honoraria for lectures or advisory boards from Biogen, Novartis, Merck Serono, Teva and Sanofi Genzyme.
Abstract: EP1689
Type: ePoster
Abstract Category: Therapy - disease modifying - 28 Long-term treatment monitoring
Background: Alemtuzumab (ALZ) is a modulatory drug for patients with relapsing-remitting multiple sclerosis (RRMS). Post-marketing surveillance is important to assess the long term safety and effectiveness in a real-world setting. ALZ has therefore been included into the Swedish post-market surveillance study “Immunomodulation and Multiple Sclerosis Epidemiology Study” upon launch in Sweden (March 2014).
Objective: To follow up the effectiveness and long-term safety of ALZ in a real-world setting.
Methods: Swedish MS patients are registered into the nationwide web-based Swedish neuro registry (neuroreg). Before ALZ initiation, patients are asked to participate in the IMSE 3 study. Adverse events (AEs) and clinical measures; extended disability status scale (EDSS), multiple sclerosis severity scale (MSSS), symbol digit modalities test (SDMT), multiple sclerosis impact scale (MSIS-29), European quality of life - 5 dimension test (EQ-5D), are obtained from neuroreg. The Wilcoxon signed-rank test was used to assess changes in effectiveness.
Results: Between March 2014 and April 2017, 104 patients (63% female; 95% RRMS) were included in the IMSE 3 study. Mean age at treatment start was 34 years. Mean number of drugs used before ALZ was 2.8 and most patients switched from Natalizumab (NTZ) (39%). In patients treated with Fingolimod (FGL) before ALZ (n=15), 47% were temporarily (≤ 5 months) treated with NTZ between FGL and ALZ start. 15% had ALZ as their very first disease modifying treatment. Six patients had discontinued ALZ treatment, of which five patients switched to another disease modifying therapy, and one patient died in association with the first ALZ treatment cycle due to fulminant viral hepatitis (Cytomegalovirus, Epstein-Barr Virus). 17 AEs were reported to the Swedish Medical Products Agency, 12 events were classified as non-serious. 97 patients had been treated for at least 12 months and 87 patients for at least 24 months. In patients treated at least 12 months significant improvements were seen for EDSS (2.10±1.57 - 1.67±1.54, n=55), MSSS (3.43±2.76 - 2.64±2.42, n=47), VAS (66.8±21.9 - 73.2±17.7, n=63) and EQ5D (0.67±0.30 - 0.76±0.25, n=70). Conclusions: Neuroreg proves to function well as a post-marketing drug surveillance platform, providing data regarding drug effectiveness and AEs. A longer follow-up period is needed to assess the real-world effectiveness and safety of ALZ.
Disclosure: The IMSE 3 study has received unrestricted grants from Sanofi Genzyme.
Åsa Leandersson has nothing to disclose.
Stina Kågström has nothing to disclose.
Linda Forsberg has nothing to disclose.
Jan Hillert has received honoraria for serving on advisory boards for Biogen, Sanofi-Genzyme and Novartis and speaker's fees from Biogen, Novartis, Merck-Serono, Bayer-Schering, Teva and Sanofi-Genzyme. He has served as P.I. for projects, or received unrestricted research support from, BiogenIdec, Merck-Serono, TEVA, Sanofi-Genzyme and Bayer-Schering.His MS research is funded by the Swedish Research Council and the Swedish Brain foundation.
Petra Nilsson has received travel support from Bayer Schering Pharma, Merck Serono, Biogen and Sanofi Genzyme, honoraria for lectures and advisory boards from Merck Serono and Sanofi Genzyme, advisory boards for Novartis and Roche, lectures for Biogen and has received unrestricted grants from Biogen.
Charlotte Dahle has received unrestricted research grants or honoraria for lectures or advisory boards from Biogen, Novartis, Merck Serono, Teva and Sanofi Genzyme.
Anders Svenningsson has nothing to disclose.
Jan Lycke has received travel support and/or lecture honoraria from Bayer Schering Pharma, Biogen, Novartis, Teva and Sanofi Genzyme; has served on scientific advisory boards for Almirall, Teva, Biogen, Novartis and Sanofi Genzyme; serves on the editorial board of the Acta Neurologica Scandinavica; has received unconditional research grants from Biogen, Novartis and Teva.
Anne-Marie Landtblom has received honoraria from Merck Serono, Teva, Biogen Sanofi Genzyme.
Joachim Burman has received travel support and/or lecture honoraria from Almirall, Biogen, Sanofi Genzyme, Hospira and Merck Serono; has received unconditional research grants from Biogen and Merck Serono.
Fredrik Walentin has received research grants from Biogen and Merck Serono.
Claes Martin has received honoraria for lectures and advisory boards from Merck Serono and Sanofi Genzyme.
Fredrik Piehl has received unrestricted academic research grants from Biogen, Genzyme and Novartis, and travel support and/or compensation for lectures and/or participation in advisory boards from Biogen, Merck Serono, Novartis, Sanofi Genzyme and Teva, which have been exclusively used for the support of research activities.
Tomas Olsson has received unrestricted research grants or honoraria for lectures or advisory boards from Biogen, Novartis, Merck Serono, Teva and Sanofi Genzyme.