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Abstract Details

Persistence and Adherence to Ocrelizumab Compared With Other Disease-Modifying Therapies for Multiple Sclerosis in US Commercial Claims Databases
Multiple Sclerosis
P9 - Poster Session 9 (12:00 PM-1:00 PM)
9-018

To understand adherence, persistence and switching patterns among patients with multiple sclerosis (MS) initiating disease-modifying therapy (DMT).

Real-world evidence characterizing treatment pathways with ocrelizumab is limited. 

This analysis used the PharMetrics Plus commercial claims database. Patients with MS initiating a new DMT in April 2017–March 2018 were observed for ≥1 year pre- and post-DMT initiation. For the initiated DMT, ≥2 prescriptions were required; completing Dose 1 met this requirement for ocrelizumab. Comparator DMTs were grouped by administration route: injectable, oral and intravenous. The proportion of days covered (PDC) was calculated as (total days of DMT supply during post-initiation year)/(365 days). One-year persistence was defined as no switch to other DMTs and no gap in supply >60 days between last fill date and the end of the post-initiation year for non-ocrelizumab DMTs; for ocrelizumab, it was defined as second dose within the post-initiation year. Treatment patterns were described for patients switching DMTs within 1 year. Multivariable Poisson regression models compared nonadherence (PDC <0.80) and discontinuation (nonpersistence) across DMTs.

A total of 2,561 patients (ocrelizumab, n=729; injectable, n=510; oral, n=1,109; intravenous, n=213) were included. Patients initiating ocrelizumab had the highest mean PDC (adherence; 91.4%) vs other groups (injectable, 73%; oral, 77%; intravenous, 81%) and the lowest proportion of patients discontinuing (9% vs 38%, 29% and 25%, respectively). A small number of patients switching from ocrelizumab within 1 year (n=7) were most likely to switch to another intravenous DMT (57%) or oral DMT (28.5%). Compared with ocrelizumab, patients initiating injectable, oral and intravenous DMTs were 2–3 times more likely to be nonadherent and 3–5 times more likely to discontinue treatment (p<0.001 for all comparisons with ocrelizumab). 

In a real-world setting, patients initiating ocrelizumab were the least likely to discontinue or switch therapy within 1 year. 

Authors/Disclosures
Natalie J. Engmann, PhD (Genentech, Inc)
PRESENTER
No disclosure on file
Daniel Sheinson No disclosure on file
No disclosure on file
Laura J. Julian, PhD (Genentech) No disclosure on file
Gabriel Pardo, MD, FÂé¶¹´«Ã½Ó³»­ (Oklahoma Medical Research Foundation) Dr. Pardo has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Roche Genentech. Dr. Pardo has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Sanofi Genzyme. Dr. Pardo has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for EMD Serono. Dr. Pardo has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Novartis. Dr. Pardo has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for TG Therapeutics. Dr. Pardo has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Amgen . Dr. Pardo has received personal compensation in the range of $5,000-$9,999 for serving on a Speakers Bureau for Bristol Myers Squibb. Dr. Pardo has received personal compensation in the range of $10,000-$49,999 for serving on a Speakers Bureau for EMD Serono. Dr. Pardo has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Novartis. Dr. Pardo has received personal compensation in the range of $5,000-$9,999 for serving on a Speakers Bureau for Roche Genentech. Dr. Pardo has received personal compensation in the range of $5,000-$9,999 for serving on a Speakers Bureau for Sanofi Genzyme. Dr. Pardo has received personal compensation in the range of $10,000-$49,999 for serving on a Speakers Bureau for TG Therapeutics. Dr. Pardo has received personal compensation in the range of $5,000-$9,999 for serving on a Speakers Bureau for Amgen. Dr. Pardo has or had stock in Progentec Diagnostics.Dr. Pardo has or had stock in Cadenza Bio.