Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis (2024)

Abstract

Background: Recently, ocrelizumab (Ocrevus®) was approved for the treatment of primary progressive multiple sclerosis (PPMS) based on data from the ORATORIO clinical trial. Real-world data about the clinical effectiveness of ocrelizumab has yet to be gathered.

Objective: The aim of this study was to provide data about the clinical effectiveness of ocrelizumab for patients diagnosed with PPMS in a real-world setting.

Methods: We conducted a retrospective cohort study of all patients with PPMS who started ocrelizumab treatment (n = 21) in St. Antonius Hospital (Utrecht/Nieuwegein, the Netherlands) between April 2018 and December 31, 2018. Primary outcome was pre- versus post-ocrelizumab disability worsening rate (from 96 weeks prior to first ocrelizumab administration up to 24 weeks post first ocrelizumab administration).

Results: Disability worsening rate while on treatment significantly differed (lower) from disability worsening rate in pre-treatment period (Z = -2.81, p ≤ .01). Three out of 17 patients showed a clinically relevant improvement in disability status after treatment start.

Conclusion: Ocrelizumab can stabilize disability progression in patients with PPMS. Some patients even showed a clinically relevant improvement in disability status. Further research should help to identify which patients benefit most from ocrelizumab.

Original languageEnglish
Article number5463451
Number of pages6
JournalMultiple Sclerosis International
Volume2020
DOIs
Publication statusPublished - 2020

Access to Document

  • 5463451Final published version, 615 KB

    Fingerprint

    Dive into the research topics of 'Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis'. Together they form a unique fingerprint.

    View full fingerprint

    Cite this

    • APA
    • Author
    • BIBTEX
    • Harvard
    • Standard
    • RIS
    • Vancouver

    Daniels, K., van der Nat, P. B., Frequin, S. T. F. M., van der Wees, P. J., Biesma, D. H., Hoogervorst, E. L. J. (2020). Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis. Multiple Sclerosis International, 2020, Article 5463451. https://doi.org/10.1155/2020/5463451

    Daniels, K ; van der Nat, P B ; Frequin, S T F M et al. / Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis. In: Multiple Sclerosis International. 2020 ; Vol. 2020.

    @article{f687cebb4ebb4069a719488f54706404,

    title = "Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis",

    abstract = "Background: Recently, ocrelizumab (Ocrevus{\textregistered}) was approved for the treatment of primary progressive multiple sclerosis (PPMS) based on data from the ORATORIO clinical trial. Real-world data about the clinical effectiveness of ocrelizumab has yet to be gathered.Objective: The aim of this study was to provide data about the clinical effectiveness of ocrelizumab for patients diagnosed with PPMS in a real-world setting.Methods: We conducted a retrospective cohort study of all patients with PPMS who started ocrelizumab treatment (n = 21) in St. Antonius Hospital (Utrecht/Nieuwegein, the Netherlands) between April 2018 and December 31, 2018. Primary outcome was pre- versus post-ocrelizumab disability worsening rate (from 96 weeks prior to first ocrelizumab administration up to 24 weeks post first ocrelizumab administration).Results: Disability worsening rate while on treatment significantly differed (lower) from disability worsening rate in pre-treatment period (Z = -2.81, p ≤ .01). Three out of 17 patients showed a clinically relevant improvement in disability status after treatment start.Conclusion: Ocrelizumab can stabilize disability progression in patients with PPMS. Some patients even showed a clinically relevant improvement in disability status. Further research should help to identify which patients benefit most from ocrelizumab.",

    author = "K Daniels and {van der Nat}, {P B} and Frequin, {S T F M} and {van der Wees}, {P J} and Biesma, {D H} and Hoogervorst, {E L J} and {van de Garde}, {E M W}",

    note = "Copyright {\textcopyright} 2020 K. Daniels et al.",

    year = "2020",

    doi = "10.1155/2020/5463451",

    language = "English",

    volume = "2020",

    journal = "Multiple Sclerosis International",

    issn = "2090-2654",

    publisher = "Hindawi Publishing Corporation",

    }

    Daniels, K, van der Nat, PB, Frequin, STFM, van der Wees, PJ, Biesma, DH, Hoogervorst, ELJ 2020, 'Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis', Multiple Sclerosis International, vol. 2020, 5463451. https://doi.org/10.1155/2020/5463451

    Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis. / Daniels, K; van der Nat, P B; Frequin, S T F M et al.
    In: Multiple Sclerosis International, Vol. 2020, 5463451, 2020.

    Research output: Contribution to journalArticleAcademicpeer-review

    TY - JOUR

    T1 - Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis

    AU - Daniels, K

    AU - van der Nat, P B

    AU - Frequin, S T F M

    AU - van der Wees, P J

    AU - Biesma, D H

    AU - Hoogervorst, E L J

    AU - van de Garde, E M W

    N1 - Copyright © 2020 K. Daniels et al.

    PY - 2020

    Y1 - 2020

    N2 - Background: Recently, ocrelizumab (Ocrevus®) was approved for the treatment of primary progressive multiple sclerosis (PPMS) based on data from the ORATORIO clinical trial. Real-world data about the clinical effectiveness of ocrelizumab has yet to be gathered.Objective: The aim of this study was to provide data about the clinical effectiveness of ocrelizumab for patients diagnosed with PPMS in a real-world setting.Methods: We conducted a retrospective cohort study of all patients with PPMS who started ocrelizumab treatment (n = 21) in St. Antonius Hospital (Utrecht/Nieuwegein, the Netherlands) between April 2018 and December 31, 2018. Primary outcome was pre- versus post-ocrelizumab disability worsening rate (from 96 weeks prior to first ocrelizumab administration up to 24 weeks post first ocrelizumab administration).Results: Disability worsening rate while on treatment significantly differed (lower) from disability worsening rate in pre-treatment period (Z = -2.81, p ≤ .01). Three out of 17 patients showed a clinically relevant improvement in disability status after treatment start.Conclusion: Ocrelizumab can stabilize disability progression in patients with PPMS. Some patients even showed a clinically relevant improvement in disability status. Further research should help to identify which patients benefit most from ocrelizumab.

    AB - Background: Recently, ocrelizumab (Ocrevus®) was approved for the treatment of primary progressive multiple sclerosis (PPMS) based on data from the ORATORIO clinical trial. Real-world data about the clinical effectiveness of ocrelizumab has yet to be gathered.Objective: The aim of this study was to provide data about the clinical effectiveness of ocrelizumab for patients diagnosed with PPMS in a real-world setting.Methods: We conducted a retrospective cohort study of all patients with PPMS who started ocrelizumab treatment (n = 21) in St. Antonius Hospital (Utrecht/Nieuwegein, the Netherlands) between April 2018 and December 31, 2018. Primary outcome was pre- versus post-ocrelizumab disability worsening rate (from 96 weeks prior to first ocrelizumab administration up to 24 weeks post first ocrelizumab administration).Results: Disability worsening rate while on treatment significantly differed (lower) from disability worsening rate in pre-treatment period (Z = -2.81, p ≤ .01). Three out of 17 patients showed a clinically relevant improvement in disability status after treatment start.Conclusion: Ocrelizumab can stabilize disability progression in patients with PPMS. Some patients even showed a clinically relevant improvement in disability status. Further research should help to identify which patients benefit most from ocrelizumab.

    U2 - 10.1155/2020/5463451

    DO - 10.1155/2020/5463451

    M3 - Article

    C2 - 32607256

    SN - 2090-2654

    VL - 2020

    JO - Multiple Sclerosis International

    JF - Multiple Sclerosis International

    M1 - 5463451

    ER -

    Daniels K, van der Nat PB, Frequin STFM, van der Wees PJ, Biesma DH, Hoogervorst ELJ et al. Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis. Multiple Sclerosis International. 2020;2020:5463451. doi: 10.1155/2020/5463451

    Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis (2024)

    FAQs

    Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis? ›

    This real-world data study confirmed that ocrelizumab can stabilize disability progression in patients with PPMS. Interestingly, three out of 17 patients even showed clinically relevant improvement in disability status.

    How effective is Ocrevus for primary progressive MS? ›

    In a large clinical trial, fewer people with PPMS taking Ocrevus had an increase in disability; people taking Ocrevus were 24% less likely to have an increase in their disability than those taking placebo.

    What is the success rate of ocrelizumab? ›

    Over one year of observation, 83.6% of ocrelizumab recipients with RMS and 93.2% with PPMS experienced treatment success (defined as no relapse, progression or treatment discontinuation due to an adverse event); mean changes in EDSS from baseline to after one year of treatment were 0.0 and 0.1 in the respective groups.

    What are the results of PPMS Ocrevus? ›

    In patients with PPMS, 36% were free from disability progression based on 48-week CDP events and 80% of those patients treated continuously with Ocrevus over 10 years were still able to walk.

    What are the results of the ocrelizumab trial? ›

    The individual trial results favoured ocrelizumab over interferon beta-1a for CDP at 12 weeks and 24 weeks in both OPERA-I (HR 0.57 [95% CI, 0.37 to 0.90] and HR 0.57 [95% CI, 0.34 to 0.95], respectively) and OPERA-II (HR 0.63 [95% CI, 0.42 to 0.92] and HR 0.63 [95% CI, 0.40 to 0.98], respectively); however, these ...

    Can Ocrevus stop MS progression? ›

    Long-term reduction in 48-week confirmed disability progression after 5 years of ocrelizumab treatment in patients with relapsing multiple sclerosis.

    What is the life expectancy of someone with primary progressive MS PPMS? ›

    This means they continue to have alternating flares and periods of recovery but will experience a steady worsening of symptoms. However, if a person has primary progressive MS (PPMS), their life expectancy is slightly lower at 71.4 years.

    What is the best treatment for primary progressive multiple sclerosis? ›

    Primary progressive multiple sclerosis (PPMS) treatments can involve ocrelizumab (Ocrevus) or stem cell therapy. Strength training exercises can also help manage symptoms.

    What is the truth about Ocrevus? ›

    Taking Ocrevus may increase your risk for cancer, including breast cancer. People who took the drug in clinical trials had a higher rate of cancer development than people who took a placebo or a similar drug. (A placebo is a treatment with no active drug.)

    Is Ocrevus worth it? ›

    Ocrevus has an average rating of 5.0 out of 10 from a total of 165 reviews on Drugs.com. 39% of reviewers reported a positive experience, while 48% reported a negative experience.

    How long after Ocrevus do you feel better? ›

    Official answer. Ocrevus has some effect at reducing disability progression within about 12 weeks; however, it may take at least 6 months or possibly longer for the full effects to be seen.

    Does PPMS ever get better? ›

    With PPMS, neurologic functions get steadily worse in the beginning. There are no symptom flare-ups (also called relapses or attacks). And there is no recovery (remission). How fast the disease progresses may vary.

    What is the new treatment for PPMS? ›

    A new drug called ocrelizumab (Ocrevus) became available for primary progressive MS in 2018. It's an infusion you have every six months. To get it you must be early on in your primary progressive MS. Depending on your level of disability, 'early' means it's been between 10 and 15 years since your MS began.

    Can Ocrevus make lesions go away? ›

    OCREVUS WAS PROVEN TO REDUCE BRAIN LESIONS ON MRI.

    T1 Gd+ lesions are thought to be a sign of active inflammation. The exact way OCREVUS works is not fully known.

    What are the positive results from Ocrevus? ›

    The results show that after 10 years of continuous Ocrevus treatment, 77% of patients with RMS had no disability progression and 92% of them continued to walk unassisted.

    Can Ocrevus make MS better? ›

    Experts believe that having too many B cells causes MS relapses (when the disease is active, and symptoms flare up). By reducing the number of these cells in your body, Ocrevus can help relieve your MS symptoms and make relapses occur less often.

    Is ocrelizumab effective? ›

    In younger people with MS, ocrelizumab is a highly effective therapy, while interferon beta and glatiramer acetate have lower efficacy.

    Does Progressive MS ever stop progressing? ›

    Primary progressive MS affects around 10 to 15% of people with MS. In this type of MS, clear periods when your disability stops or gets a bit better are extremely rare.

    What is the success rate of Ocrevus? ›

    90% of patients treated with OCREVUS showed no 12-week or 24-week confirmed disability progression in the controlled period.

    Can progressive MS be reversed? ›

    There is no cure for multiple sclerosis (MS), but there has been much progress in developing new drugs to treat it. Research is ongoing to develop new and better disease-modifying therapies (DMTs) for this disease of the central nervous system.

    How many cases of PML with Ocrevus are there? ›

    During this time, a total of 12 cases of PML were confirmed (Table 1). All 12 cases were confirmed in the setting of presence of JCV DNA in CSF along with a brain MRI consistent with the diagnosis of PML.

    Is Ocrevus highly effective? ›

    90% of patients treated with OCREVUS showed no 12-week or 24-week confirmed disability progression in the controlled period.

    How quickly does primary progressive MS progress? ›

    The authors of a 2015 study reported that the average time that it takes for a person with a diagnosis of PPMS to reach a score of 4.0 is 8.1 years. The authors also found that the time it takes to reach 8.0 can vary, but on average, this takes about 20.7 years.

    References

    Top Articles
    Latest Posts
    Article information

    Author: Mr. See Jast

    Last Updated:

    Views: 5320

    Rating: 4.4 / 5 (55 voted)

    Reviews: 86% of readers found this page helpful

    Author information

    Name: Mr. See Jast

    Birthday: 1999-07-30

    Address: 8409 Megan Mountain, New Mathew, MT 44997-8193

    Phone: +5023589614038

    Job: Chief Executive

    Hobby: Leather crafting, Flag Football, Candle making, Flying, Poi, Gunsmithing, Swimming

    Introduction: My name is Mr. See Jast, I am a open, jolly, gorgeous, courageous, inexpensive, friendly, homely person who loves writing and wants to share my knowledge and understanding with you.