Treatment Landscape of Multiple Sclerosis in Mosul: A Descriptive Cross-Sectional Study at Ibn-Sina Neurology Center
Abstract
Background: Multiple sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system that encompasses long-term usage of disease-modifying therapy (DMTs). In Mosul city, the availability, distribution, prescription patterns, and accessibility of such therapies is not fully explored.
Objective: To describe the current treatment landscape for MS patients at Mosul Neurology Center, including DMT usage patterns, common adverse effects reasons for therapy switching, age and gender distribution of patients, local drug availability and cost, patient satisfaction, and infrastructure conditions at the local biological therapy unit.
Methods: This descriptive cross-sectional study analyzed a random sample of 108 medical records drawn from a total cohort of 592 registered MS patients at Ibn-Sina Neurology Center. Collected data included age, gender, current DMT, prior treatment history, therapy switching, and relevant laboratory findings. The annual treatment cost of each drug class was assessed. Additionally, a structured patient questionnaire was performed in the biological therapy unit. Drug usage patterns were compared with UK and other global benchmarks.
Results: Eight drugs are currently used in the treatment spectrum of 592 registered MS patients. The pattern is coherent with international standards, but there is relatively high utilization of betaferon (21% of patients), and lack of other more useful options, like dimethyl fumarate. Fingolimod is associated with high rate of leukopenia, and betaferon is the most commonly discontinued drug. Treatment pattern is consistent with induction strategy, and analysis of annual cost shows that natalizumab is the most expensive, yet, valuable drug, followed by ocrelizumab and betaferon. Generally, 60% of patients receiving biological treatment are completely satisfied with their treatment.
Conclusion: The available DMTs landscape is fairly good, including the usage of multiple treatment options and continuous monitoring of adverse reactions. Yet, it can still be improved by reallocating resources from high-cost, lower-efficacy interferons to introducing oral agents like dimethyl fumarate.
References
- Absinta M, Sati P, Masuzzo F, Nair G, Sethi V, Kolb H, et al. Association of chronic active multiple sclerosis lesions with disability in vivo. JAMA Neurol. 2019;76(12):1474–83. doi:10.1001/jamaneurol.2019.2399.
- Taher YQM, Ahmed MM, Majdal HM. Multiple Sclerosis in Ninevah: Epidemiological and clinical study. Azerbaijan Med Assoc J. 2022;62(4):1277–88.
- Kern DM, Cepeda MS. Treatment patterns and comorbid burden of patients newly diagnosed with multiple sclerosis in the United States. BMC Neurol. 2020;20(1):296. doi:10.1186/s12883-020-01882-2.
- Disanto G, Berlanga AJ, Handel AE, Para AE, Burrell AM, Fries A, et al. Heterogeneity in multiple sclerosis: scratching the surface of a complex disease. Autoimmune Dis. 2010;2011:932351. doi:10.4061/2011/932351.
- Brancati S, Gozzo L, Longo L, Vitale DC, Drago F. Rituximab in multiple sclerosis: Are we ready for regulatory approval? Front Immunol. 2021;12:661882. doi:10.3389/fimmu.2021.661882.
- Perrone V, Veronesi C, Giacomini E, Citraro R, Dell'Orco S, Lena F, et al. The epidemiology, treatment patterns and economic burden of different phenotypes of multiple sclerosis in Italy. Clin Epidemiol. 2022;14:1327–37. doi:10.2147/CLEP.S376005.
- Danafar P, Nourikhani M, Beigverdi H, Fazel M, Fazeli MM, Shariat Mostafavi FS, et al. A brief review of multiple sclerosis treatments. Int J Clin Stud Med Case Rep. 2022;19:000467. doi:10.46998/IJCMCR.2022.19.000467.
- Lucchinetti C, Brück W, Parisi J, Scheithauer B, Rodriguez M, Lassmann H. Heterogeneity of multiple sclerosis lesions: implications for the pathogenesis of demyelination. Ann Neurol. 2000;47(6):707–17.
- doi:10.1002/1531-8249(200006)47:6<707::aid-ana3>3.0.co;2-q.
- Almatrafi YM, Babakkor MA, Irfan M, Samkari ET, Alzahrani WM, Mohorjy DK, et al. Efficacy and safety of rituximab in patients with multiple sclerosis: An observational study at a tertiary center in Makkah, Saudi Arabia. Neurosciences (Riyadh). 2022;27(2):65–70. doi:10.17712/nsj.2022.2.20210122.
- Metz I, Weigand SD, Popescu BF, Frischer JM, Parisi JE, Guo Y, et al. Pathologic heterogeneity persists in early active multiple sclerosis lesions. Ann Neurol. 2014;75(5):728–38. doi:10.1002/ana.24163.
- Rae-Grant A, Day GS, Marrie RA, Rabinstein A, Cree BAC, Gronseth GS, et al. Disease-modifying therapies for adults with multiple sclerosis: Report of the Guideline Development Subcommittee of the AAN. Neurology. 2018;90(17):789–800. doi:10.1212/WNL.0000000000005345.
- Lee CY, Chan KH. Personalized use of disease-modifying therapies in multiple sclerosis. Pharmaceutics. 2024;16(1):120. doi:10.3390/pharmaceutics16010120.
- Finkelsztejn A. Multiple sclerosis: overview of disease-modifying agents. Perspect Med Chem. 2014;6:65–72. doi:10.4137/PMC.S13213.
- Olejnik P, Roszkowska Z, Adamus S, Kasarełło K. Multiple sclerosis: a narrative overview of current pharmacotherapies and emerging treatment prospects. Pharmacol Rep. 2024;76(5):926–43. doi:10.1007/s43440-024-00642-0.
- Guger M, Enzinger C, Leutmezer F, Di Pauli F, Kraus J, Kalcher S, et al. Early intensive versus escalation treatment in patients with relapsing-remitting multiple sclerosis in Austria. J Neurol. 2024;271(6):3142–52. doi:10.1007/s00415-024-12256-w.
- Prosperini L, Mancinelli CR, Solaro CM, Nociti V, Haggiag S, Cordioli C, et al. Induction versus escalation in multiple sclerosis: A 10-year real world study. Neurotherapeutics. 2020;17(3):994–1004.
- doi:10.1007/s13311-020-00847-0.
- Zhao T, Taylor BV, Campbell JA, Palmer AJ. The disease-modifying therapy utilisation and cost trend for multiple sclerosis in Australia between 2013 and 2022. Mult Scler. 2024;30(1):80–8. doi:10.1177/13524585231213230.
- Spelman T, Herring WL, Zhang Y, Tempest M, Pearson I, Freudensprung U, et al. Comparative effectiveness and cost-effectiveness of natalizumab and fingolimod in patients with inadequate response to DMTs. Pharmacoeconomics. 2022;40(3):323–39. doi:10.1007/s40273-021-01106-6.
- Langer-Gould A, Sotirchos ES, Bourdette D. Rituximab for multiple sclerosis: Hiding in plain sight. Neurology. 2024;102(2):e208063. doi:10.1212/WNL.0000000000208063.
- Mathew T, John SK, Kamath V, Murgod U, Thomas K, Baptist AA, et al. Efficacy and safety of rituximab in multiple sclerosis: Experience from a developing country. Mult Scler Relat Disord. 2020;43:102210. doi:10.1016/j.msard.2020.102210.
- Zhang Y, Salter A, Jin S, et al. Disease-modifying therapy prescription patterns in people with multiple sclerosis by age. Ther Adv Neurol Disord. 2021;14. doi:10.1177/17562864211006499.
- Alharbi MA, Aldosari F, Althobaiti AH, Abdullah FM, Aljarallah S, Alkhawajah NM, et al. Clinical and economic evaluations of natalizumab, rituximab, and ocrelizumab for RRMS in Saudi Arabia. BMC Health Serv Res. 2023;23(1):552. doi:10.1186/s12913-023-09462-z.
- Hauser SL, Cree BAC. Treatment of multiple sclerosis: a review. Am J Med. 2020 Dec;133(12):1380-1390.e2. doi: 10.1016/j.amjmed.2020.05.049.
- Berntsson SG, Kristoffersson A, Boström I, Feresiadou A, Burman J, Landtblom AM. Rapidly increasing off-label use of rituximab in MS in Sweden – Outlier or predecessor? Acta Neurol Scand. 2018;138(4):327–31. doi:10.1111/ane.12963.
- Multiple Sclerosis International Federation. Proportion of people treated with each DMT – United Kingdom [Internet]. London: Atlas of MS; c2020 [cited 2025 Jul 20]. Available from: https://atlasofms.org/table/united-kingdom/disease-modifying-treatments/proportion-of-people-treated-with-each-dmt



