- Research article
- Open Access
The real-world patient experience of fingolimod and dimethyl fumarate for multiple sclerosis
BMC Research Notesvolume 9, Article number: 434 (2016)
Oral disease-modifying therapies offer equivalent or superior efficacy and greater convenience versus injectable options.
To compare patient-reported experiences of fingolimod and dimethyl fumarate.
Adult relapsing-remitting multiple sclerosis patients treated with fingolimod or dimethyl fumarate were recruited from an online patient community and completed an online survey about treatment side effects, discontinuation, and satisfaction.
281 patients in four groups completed the survey: currently receiving fingolimod (CF, N = 61), currently receiving dimethyl fumarate (CDMF, N = 129), discontinued fingolimod (DF, N = 32) and discontinued dimethyl fumarate (DDMF, N = 59). Reasons for treatment switch were to take oral treatment (CF: 63.3 %, CDMF: 61.8 %), side effects of prior medication (CF: 67.3 %, CDMF: 44.1 %) and lack of effectiveness of prior medication (CF: 38.8 %, CDMF: 31.4 %). Main reasons for discontinuation were side effects (DF: 46.9 %, DDMF: 67.8 %) and lack of effectiveness (DF: 25.0 %, DDMF: 15.3 %). CDMF patients had an increased risk of abdominal pain, flushing, diarrhea, and nausea. Treatment satisfaction was highest among CF patients followed by CDMF, DF, and then DDMF patients.
Discontinuation was driven by experience of side effects. Patients currently taking dimethyl fumarate were more likely to experience a side effect versus patients currently taking fingolimod. Examination of the relationship between tolerability and adherence/persistence is needed.
Multiple sclerosis (MS) is a chronic inflammatory demyelinating condition of unknown etiology. It is one of the most common diseases of the central nervous system, affecting more than 2.3 million people worldwide . Approximately 90 % of patients have the relapsing-remitting form of MS (RRMS) initially . With no known cure, disease-modifying therapies (DMTs) aim to prevent relapses, as well as delay the accumulation of disease burden and disability . From 1993 until recently, DMTs approved by the US Food and Drug Administration (FDA) were in injectable form, but these have been associated with sub-optimal adherence, and increased risk of relapse and accumulation of disease burden . Reasons for non-adherence include injection-related factors, as well as side effects of the medications themselves [4–6].
Fingolimod (Gilenya®, Novartis Pharmaceuticals Corporation) , an oral DMT approved by the FDA in 2010, has shown to have superior efficacy to a comparator injectable DMT  and there is evidence of higher adherence and persistence, thought to be attributable in part to the improved tolerability profile as well as the mode of administration [2, 5]. Although fingolimod is well-tolerated, it requires monitoring for 6 h after administering the first dose. Dimethyl fumarate (Tecfidera®, Biogen) , approved by the FDA in 2013, is another oral DMT with favorable efficacy to injectable DMTs . Unlike fingolimod, dimethyl fumarate requires no monitoring, but reports suggest it has been challenging for some patients to tolerate, particularly within the first 60 days of initiating treatment .
Tolerability of fingolimod and dimethyl fumarate has been assessed in clinical trials and retrospective studies [2, 5, 12], rather than in less-controlled, real-world population studies. This study was designed to explore the real-world, patient-reported experiences associated with initiating treatment with either fingolimod or dimethyl fumarate. The specific objectives of this patient-reported study were to compare the side effect experiences of patients on fingolimod and dimethyl fumarate, to compare the levels of treatment satisfaction or dissatisfaction between fingolimod and dimethyl fumarate with regard to effectiveness, side effects and convenience and to describe other patient-reported outcomes related to social impact and disability.
This was a cross-sectional observational study in which patients with RRMS in the United States with current or past experience of fingolimod or dimethyl fumarate completed a web-based survey.
A draft online survey comprising a battery of measures was developed. The first section included questions about nine medication-specific side effects representing the top five side effects that could be perceived by patients for each of the two products based on incidence versus placebo as reported in the FDA product labels for each product (fingolimod: back pain, cough, diarrhea, headache, influenza; dimethyl fumarate: abdominal pain, diarrhea, flushing, nausea, vomiting) [7, 9]. The labelled side effect “influenza” was asked of patients in the survey as “flu-like symptoms.” All participants were presented with the same set of nine side effects.
The treatment satisfaction questionnaire for medication (TSQM), a 14-item scale measuring patient satisfaction with medication, including side effects, effectiveness, convenience, and global satisfaction , was administered. All TSQM scores range from 0 to 100, of which higher scores indicate greater treatment satisfaction.
A single item was developed to assess the impact of MS on social activities over the past 4 weeks, with five verbal response options (‘none of the time’ to ‘all of the time’).
Disability status was assessed using the multiple sclerosis rating scale-revised (MSRS-R), a patient-reported measure of MS-related functional status that has been validated psychometrically  and clinically in a population of patients with RRMS . The scale covers the functional domains of “Walking,” “Using arms and hands,” “Vision,” “Speaking clearly,” “Swallowing,” “Bowel or bladder dysfunction,” “Thinking/Cognition/Memory,” and “Numbness/Tingling/Burning Sensation/Pain.” Scores for each scale range from 0 to 4, and the Total MSRS-R score ranges from 0 to 32, of which higher scores indicate greater disability. Disability was assessed using the patient-determined disease steps (PDDS) questionnaire , a 9-level scale providing a score indicating the patient-reported level of overall disability, ranging from 0 (i.e. normal walking) to 9 (i.e. bedridden).
The draft survey underwent pilot testing in which 5 patients completed the survey online and participated in an interview to provide feedback on the clarity and appropriateness of instructions, items and response options. Based on feedback, minor changes in the wording of items were made to improve clarity or to maintain consistency across similar items, and additional response options were added to some items to fully capture possible options.
Study participants were recruited from an online patient community, PatientsLikeMe, a patient-powered research network that allows patients with MS to interact, track their health data over time, contribute to research , and improve their self-management . All participants in the online community reporting that they had been diagnosed with MS by a physician were invited via email and provided with a URL to the online screener. Eligibility criteria included reported diagnosis of RRMS, current or past experience of treatment with fingolimod or dimethyl fumarate, aged 18 or older, and fluency in English. Any patient who reported they were enrolled in a clinical trial was also excluded from participation. Prior treatment with other DMTs was permitted. If they met the eligibility criteria, participants were presented with an online informed consent form, and only those who consented proceeded to the online survey. In order to have sufficient experience with either medication, participants must have been on either treatment for a minimum of 7 days so that patients would have had time to experience the product and, for those on fingolimod, to have completed the early monitoring phase; anyone who had initiated treatment less than 7 days prior to screening was asked to wait to complete the survey until they had been on treatment for at least 7 days. In this case, the participant was sent a reminder email after the 8th day of treatment to complete the survey. The study protocol was approved by New England IRB (Newton, MA). Participants were not remunerated for taking part in the study; at the end of the study all participants who completed the survey were emailed a brief report summarizing the findings.
The primary analyses included all eligible participants who responded to the survey according to the following defined four study groups: participants currently receiving fingolimod (CF), participants currently receiving dimethyl fumarate (CDMF), participants who started and then discontinued fingolimod (DF), and those who started and then discontinued dimethyl fumarate (DDMF). Any patient who fell into more than one group based on treatment experience was assigned to a group based on his or her most recent treatment experience. For example, if a patient discontinued fingolimod and dimethyl fumarate, the patient was assigned to a group based on the treatment the patient was on most recently.
For each study group (i.e., CF, CDMF, DF, DDMF), descriptive statistics, including mean, standard deviation, and range for continuous variables, and frequency for categorical variables, were generated for medication-specific side effects of interest, the four scales of the TSQM, the single social functioning item, the PDDS questionnaire, the MSRS-R and for demographic and clinical characteristics. Descriptive statistics were generated for patients in the DF and DDMF groups to summarize characteristics related to therapy discontinuation.
Logistic regression models were employed to determine the association between study group (CF vs. CDMF) and the occurrence of side effects (Yes/No). Due to the small number of events observed for some side effects, a modification to the logistic regression models was implemented in an attempt to minimize potential bias due to quasi-complete separation of data. Hence, the Firth penalized-likelihood approach was used in all logistic regression models so that the issue of small sample sizes and separation of data points was addressed in the analysis . For each side effect, two logistic regression models were generated: a univariable model and a multivariable model that adjusted for age, gender, and Total MSRS-R score. Age and Total MSRS-R score were included as continuous variables, while gender (male vs. female) was included as a categorical variable. Additionally, the occurrence of any side effect (i.e., the indication of any of the listed side effects) was also modeled as one of the outcomes.
An analysis of variance (ANOVA) model and an analysis of covariance (ANCOVA) model were utilized to determine the association between study groups (CF vs. CDMF) and each scale of the TSQM score. In the ANOVA model, the only independent variable was study group (CF or CDMF). In the ANCOVA model, the independent variables were the same as in the multivariable logistic regression models. For each study group the least-squares mean was presented along with the 95 % confidence interval and p value. These same statistics were also presented for the difference between study groups, and this difference represented the main measure of association of study group effect. Because the objective of this study was not to prove or disprove a specific hypothesis, no threshold alpha value was set upon which to make a decision of significance. Due to the exploratory nature of these analyses, all p values were interpreted as descriptive statistics. Sponsorship for this study and article processing charges was funded by Novartis Pharmaceuticals Corporation.
The survey was fielded from 3 April 2014 to 8 August 2014. A total of 6256 patients were invited, 470 were screened as eligible, 206 were screened as ineligible (per inclusion and exclusion criteria) and a total of 283 completed the survey. Two patients were excluded from the analysis because their data indicated they had initiated current therapy less than 7 days prior to survey completion. The final sample sizes for the 281 eligible survey completers were as follows: CF (N = 61), CDMF (N = 129), DF (N = 32), DDMF (N = 59). Demographic and clinical characteristics for the study sample are presented in Table 1. Overall, observed underlying demographic and clinical characteristics were generally similar across all study groups; however, the sample was generally overrepresented by the female gender, especially in the DF and DDMF subgroups.
Across both current therapy groups, the most commonly reported MS medication taken before initiating current therapy was Copaxone (glatiramer acetate) (see Table 2). CF patients were more likely to have taken Copaxone as their most recent prior therapy (CF: 27.9 %, CDMF: 19.4 %), while CDMF patients were more likely to have taken a break from treatment before starting dimethyl fumarate (CDMF: 9.3 %, CF: 1.6 %,) or to have taken Rebif® (interferon beta-1a) as their most recent prior therapy (CDMF: 18.6 %, CF: 8.2 %). Side effects of prior medication were cited by 67.3 % of CF and 44.1 % of CDMF patients as a reason for switching to current therapy. Other commonly reported reasons were: wanting to take oral treatment (CF: 63.3 %, CDMF: 61.8 %), perceived lack of effectiveness of previous medication (CF: 38.8 %, CDMF: 31.4 %), struggling to take previous medication as prescribed (CF: 32.7 %, CDMF: 15.7 %), and concerns regarding safety of previous medication (CF: 28.6 %, CDMF: 27.5 %).
Among the discontinued groups, DDMF patients were more likely than DF to indicate side effects as one of the reasons for discontinuing therapy (78.0 vs. 43.8 %, respectively) (see Table 3). When asked to provide the main reason for discontinuation, the three most common responses were side effects (DF: 46.9 %, DDMF: 67.8 %), lack of effectiveness (DF: 25.0 %, DDMF: 15.3 %), and another reason not listed (DF: 15.6 %, DDMF: 10.2 %). Approximately half of the patients in each group indicated that the decision to discontinue therapy was a joint decision between the respondent and his or her doctor. A slightly greater percentage of DDMF patients (40.7 %) reported that the decision was mainly theirs compared to DF patients (28.1 %), but the overall distribution of responses between groups was similar.
Among the current therapy groups, CDMF patients were more likely than CF patients to report abdominal pain, diarrhea, flushing, flu-like symptoms, and nausea as treatment side effects (see Table 4). The reported occurrence of the remaining side effects was similar between the two groups. Logistic regression model results summarizing the treatment effect in predicting the occurrence of each side effect are presented in Table 5. After adjusting for covariates, CDMF patients had an increased risk of experiencing abdominal pain (odds ratio, i.e. OR 15.79), flushing (OR 12.51), and any of the solicited side effects (OR 7.49). Results from the univariable model and the multivariable model yielded similar results. Other side effects for which a pronounced increase in risk was observed for CDMF patients after adjustment were diarrhea (OR 2.30) and nausea (OR 3.16).
Among patients in the discontinued therapy groups, a group effect was observed with DDMF patients more than twice as likely to experience the following side effects (DDMF vs. DF): abdominal pain (57.6 vs. 15.6 %), diarrhea (44.1 vs. 15.6 %), flushing (72.9 vs. 25.0 %), nausea (52.2 vs. 18.8 %), and vomiting (28.8 vs. 6.3 %). The reported occurrence of the remaining side effects were more similar between discontinued therapy groups (DDMF vs. DF): back pain (20.3 vs 12.5 %), cough (10.2 vs. 12.5 %), headache (44.1 vs. 31.3 %), and flu-like symptoms (27.1 vs. 21.9 %).
ANCOVA analyses modeling TSQM scores as a function of study group (CF vs. CDMF) are presented in Table 6. CF patients on average had better convenience scale scores (8.1 points higher than CDMF patients) and better side effects scale scores (9.5 points higher than CDMF patients). There was no difference between the two groups on the “Effectiveness” scale. Differences between the groups in the global score indicate a marginal treatment effect related to overall treatment satisfaction favoring the CF group.
As expected, treatment satisfaction scores for the discontinued therapy groups were lower than the scores for the current therapy groups across all TSQM scales. However, DF patients tended to have higher mean treatment satisfaction scores than DDMF patient across all TSQM scales: effectiveness (DF: 41.7, SD = 27.3 vs. DDMF: 27.3, SD = 20.4), convenience (DF: 88.9, SD = 13.5 vs. DDMF: 79.1, SD = 20.8), side effects (DF: 81.0, SD = 36.5 vs. DDMF: 49.5, SD = 39.2), global score (DF: 28.3, SD = 25.1 vs. DDMF: 14.4, SD = 17.5) (results not tabulated).
This study provides real-world evidence of the tolerability and overall treatment satisfaction among patients with RRMS using fingolimod and dimethyl fumarate. As seen in randomized, controlled trials and clinical studies, side effects associated with dimethyl fumarate (i.e., abdominal pain, diarrhea, flushing, nausea, vomiting) were more commonly experienced by those in the dimethyl fumarate group, supporting other reports of the side effect profile of this treatment . However, the frequency of side effects associated with fingolimod (i.e., back pain, cough, diarrhea, headache, influenza) was comparable between groups. Among study participants, the odds ratio of experiencing a side effect was approximately seven, in favor of fingolimod over dimethyl fumarate. Associations remained strong after multivariable adjustment for age and disability, including after a second multivariable model adjusting for PDDS instead of MSRS-R as the measure of disability.
For both treatment groups, discontinuation was commonly driven by the experience of side effects. This was particularly evident for dimethyl fumarate, with 68 % of patients reporting “experience of side effects” as the main reason for discontinuation, and more patients in this group deciding unilaterally to stop treatment. Discontinuation of fingolimod was more frequently reported to result from a lack of perceived efficacy (25 %) than dimethyl fumarate (15 %). Compared to patients taking dimethyl fumarate, those currently taking fingolimod were more satisfied with treatment overall and specifically with regard to side effects and convenience. This was also true among the discontinued patients, with those who had discontinued fingolimod reporting greater treatment satisfaction than those who had discontinued dimethyl fumarate. However, perception of treatment effectiveness was similar between the dimethyl fumarate and fingolimod groups and use of the former drug appeared to be twice as frequent in this sample. After adjusting for underlying group characteristics, the similar perceived efficacy remained the same.
Studies in diseases involving long-term treatments have shown an association between side effects and poor compliance [19–21]. Additionally, studies among MS patients have shown that increased adherence leads to better patient outcomes and reduced healthcare utilization [5, 22, 23]. Thus, DMTs with better tolerability have the potential to improve outcomes and reduce resource use for RRMS patients, as a result of increased adherence.
Despite the consistency of results, there are several limitations of the study that should be noted. The small sample sizes did not allow for the detection of potential trends between the treatment groups. Although other oral DMTs such as teriflunomide (Aubagio®, Biogen) have recently been approved for use in RRMS, this study was limited to the two DMTs most commonly used at the time on PatientsLikeMe. Because accurate data were not publicly available to describe the true demographics of this subset of the MS population, it was not possible to use benchmark weighting to try to control for such differences. Additionally, many patients had started therapy several months before completing the survey, and given that all data was patient-reported, there is the potential for recall error regarding medication use, the side effects experienced or reasons for discontinuation. Those who agreed to participate might not be representative of the population of RRMS patients at large, who may not use internet, health-sharing sites, nor complete online surveys. Finally, the cross-sectional study design limited the ability to ascertain how the side effect experience may affect longer term adherence or prognostic outcomes.
In conclusion, the patient experience of fingolimod and dimethyl fumarate was similar for some measures and favored fingolimod for others. Future research involving a larger sample and a longitudinal design would be useful to provide further insights on real-world patient experiences and to examine the relationship between tolerability and adherence/persistence.
analysis of covariance
analysis of variance
currently receiving dimethyl fumarate
currently receiving fingolimod
discontinued dimethyl fumarate
Food and Drug Administration
multiple sclerosis rating scale-revised
patient-determined disease steps questionnaire
relapsing-remitting multiple sclerosis
treatment satisfaction questionnaire for medication
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PW contributed to study design, survey programming, data collection and analysis, and review of the manuscript. LR, BK, and RS contributed to study design, analysis, and review of the manuscript. EF contributed to study and survey design, and preparation of the manuscript. BN contributed to study and survey design, and review of the manuscript. All authors read and approved the final manuscript.
Rahul Sasané is employed by Novartis Pharmaceuticals Corporation, which manufactures fingolimod. Paul Wicks and Bo Katic are employed by PatientsLikeMe; and Lawrence Rasouliyan, Beenish Nafees, and Emuella Flood are employed by ICON, which were commissioned by Novartis Pharmaceuticals Corporation to perform the study.
All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this manuscript, take responsibility for the integrity of the work as a whole, and have given final approval to the version to be published.
Availability of data and materials
Data will not be shared due to confidentiality reasons.
Ethics approval and consent to participate
All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1964, as revised in 2013. Informed consent was obtained from all patients for being included in the study. Ethics approval was obtained from New England Institutional Review Board (NEIRB #14-053).
Sponsorship for this study and article processing charges was funded by Novartis Pharmaceuticals Corporation.