Skip to main content
Erschienen in: Neurology and Therapy 1/2019

Open Access 31.01.2019 | Original Research

Real-World Characterization of Dimethyl Fumarate-Related Gastrointestinal Events in Multiple Sclerosis: Management Strategies to Improve Persistence on Treatment and Patient Outcomes

verfasst von: Jinny Min, Stanley Cohan, Enrique Alvarez, Jacob Sloane, J. Theodore Phillips, Anneke van der Walt, Irene Koulinska, Fang Fang, Catherine Miller, Andrew Chan

Erschienen in: Neurology and Therapy | Ausgabe 1/2019

Abstract

Introduction

Delayed-release dimethyl fumarate (DMF) is an effective treatment for multiple sclerosis (MS). Some patients experience gastrointestinal (GI) adverse events (AEs) that may lead to premature DMF discontinuation. This study characterized the impact of site-specific GI management strategies on the occurrence of GI events and discontinuation patterns.

Methods

Data on GI events and DMF persistence were retrospectively abstracted from medical records of patients treated with DMF in routine medical practice in the EFFECT study (NCT02776072). GI management strategies were assessed via a study site questionnaire. Discontinuation rates were analyzed according to counseling patterns.

Results

Of 826 DMF-treated patients at 66 sites, 809 from 65 sites were eligible for the GI analysis; of these, 27% experienced GI AEs. Within 1 year of treatment, 14% (118/826) of patients discontinued DMF, 5% (44/809) due to GI events. Most sites (92%) reported that patients were very likely (> 75% of the time) to be counseled about GI events at/before DMF treatment initiation and/or to be recommended that DMF be taken with food (86%); 48% of sites reported to be very likely to recommend using symptomatic therapies for GI AEs. Lower discontinuation rates were reported at sites very likely versus not very likely (≤ 75% of the time) to (1) provide counseling; (2) provide specific details regarding GI events; or (3) recommend taking DMF with food, and/or using symptomatic GI therapies.

Conclusion

Counseling and other GI management strategies at initiation of DMF treatment appear to reduce the burden of GI events, and a variety of GI management strategies may improve DMF persistence.

Trial Registration

NCT02776072.

Funding

Biogen (Cambridge, MA, USA).
Hinweise

Electronic supplementary material

The online version of this article (https://​doi.​org/​10.​1007/​s40120-019-0127-2) contains supplementary material, which is available to authorized users.

Enhanced digital features

To view enhanced digital features for this article go to https://​doi.​org/​10.​6084/​m9.​figshare.​7588421.

Introduction

Delayed-release dimethyl fumarate (DMF) is an oral treatment option for patients with relapsing–remitting multiple sclerosis (RRMS). Upon oral administration, DMF is rapidly converted to its active metabolite monomethyl fumarate [1], which is then widely distributed throughout the body [2, 3]. DMF has demonstrated significant and sustained therapeutic efficacy across a range of clinical and radiologic measures in phase 3 clinical trials and in a long-term extension study, ENDORSE [46]. The overall safety and tolerability profile of DMF is favorable, although patients often experience gastrointestinal (GI) adverse events (AEs), such as diarrhea, nausea, abdominal pain, vomiting, and dyspepsia [7]. Clinical trials and community-based real-world studies have indicated that GI tolerability issues, if experienced, occur most frequently within the first 10–12 weeks of DMF treatment initiation, with the incidence decreasing over time. Thus, it is important that counseling patients regarding potential GI AEs occurs at or before treatment initiation [4, 610]. Although most treatment-emergent GI AEs are generally mild or moderate in nature [11], these events may lead to poor treatment compliance or premature DMF discontinuation for some patients.
In a pooled analysis of patients who received placebo (n = 771) or DMF 240 mg twice daily (n = 769) in the 2-year, randomized, double-blind, placebo-controlled phase 3 DEFINE and CONFIRM clinical trials, 31–40% of patients reported GI AEs, with < 1–3% of patients discontinuing DMF due to these events [7]. However, a multicenter, open-label, single-arm study (MANAGE) and other real-world, practice-based studies have reported discontinuation rates of 10–29% for all AEs and 7–14% for GI-specific AEs [8, 12, 13].
As of July 31, 2018, > 340,000 patients have received DMF treatment, representing > 625,000 patient-years of exposure [14]. Therefore, real-world DMF data can offer important, potentially more generalizable, insights into management strategies for GI AEs. In order to capture the levels and types of consensus on best practice management strategies from DMF prescribers, a Delphi study was conducted among North American clinicians [10]. Clinicians completed two rounds of questionnaires developed by a steering committee; consensus in round 2 was considered to be attained if ≥ 70% of respondents agreed on a particular strategy. The Delphi consensus on effective GI management strategies, as well as a preliminary report suggesting that individual patient coaching leads to decreased avoidable therapy discontinuation due to GI AEs [10, 15], was utilized to guide this research [10].
The EFFECT study (NCT02776072) was undertaken to evaluate the comparative effectiveness of DMF in patients with RRMS in both a clinical practice setting and in a subset of newly diagnosed patients. As part of the EFFECT study, a GI analysis was designed to further investigate (1) the strategies to manage and mitigate DMF-associated GI events in the real-world setting and (2) the type of GI AEs occurring in a real-world setting, GI AEs leading to treatment discontinuation, and the frequency of GI event management strategies used in patients treated with DMF [16].

Methods

Study Design and Patients

The EFFECT study was a global, multicenter, medical chart abstraction study in patients with RRMS treated with select disease-modifying therapies [DMTs; i.e., DMF, glatiramer acetate (GA), teriflunomide, or fingolimod] according to routine clinical practice [Electronic Supplementary Material (ESM) Fig. S1]. Key patient inclusion criteria were written informed consent; age ≥ 18 years; diagnosis of RRMS per 2010 McDonald criteria [17]; DMF treatment initiation after January 2011 with ≥ 12 months of follow-up data available following DMF initiation; treatment naive or have had only one prior DMT [interferon (IFN) or GA]; and multiple sclerosis relapse history for up to 3 years. Patients were included irrespective of total time on treatment. Key exclusion criteria were diagnosis of a progressive form of MS before or during data collection; prior treatment with a DMT other than IFN or GA; treatment with any formulations of DMF or compounded fumarates prior to DMF treatment initiation; and concurrent enrollment in any interventional clinical trial of an investigational product during the time of medical chart abstraction.
The GI analysis was conducted at sites that abstracted data from patients receiving DMF treatment. Sites were selected based on feasibility assessment of willingness and capability for participation in the study. Factors such as approximate number of patients treated with MS therapies, site start-up timelines, ability to retrospectively identify eligible medical records, and resources available for chart abstraction were considered. Chart abstraction occurred from May 2016 through January 2017.
Medical charts were reviewed at a single time point, and patient information was captured and managed by study sites on web-based electronic case report forms. Data were collected for patients receiving DMF for selected GI AEs and included type of event, date of onset, duration of event, concomitant treatment received, and any interruption, dose reduction, or discontinuation of DMF treatment. Physicians or their designees completed a structured, site-level questionnaire to report the likelihood of executing strategies for mitigating and/or managing GI events that may be experienced by DMF-treated patients. Responses from the questionnaire were collected to evaluate GI management practices (ESM Fig. S1) using the scale described below and were reported in the aggregate as frequencies.

Outcomes

The GI analysis endpoints were the proportion of DMF discontinuations related to selected GI events overall, by site, and by patient demographics, as well as the frequency of each strategy used for mitigating and managing GI events. A post hoc analysis assessed GI events and discontinuation rates according to survey responses to evaluate the impact of counseling on clinical outcomes.

Questionnaire to Evaluate GI Management Practices

The structured questionnaire for evaluating GI management practices consisted of a total of 26 items assessing the site characteristics, respondent type (e.g., neurologist, nurse practitioner), resources used for counseling, counseling habits (as outlined in the questionnaire, see ESM Appendix S1), and GI AE mitigation techniques. The questionnaire was built to assess the likelihood that sites were utilizing the techniques recommended by physicians using the Delphi consensus methodology to manage or mitigate GI events with DMF [10]. The questionnaire was developed in collaboration with physician and nurse healthcare providers (HCPs) and was piloted in a separate group of HCPs to assess for clarity and comprehension of the individual questions and to assess the duration of time required to complete the questionnaire.
Each site completed one questionnaire, responding to as many questions as possible. Sites were asked to describe their practice center, including size, type, and available staff. Sites also indicated the likelihood of various GI management and counseling strategies using a scale as follows:
  • Not very likely (≤ 75%)
    • Never (0%)
    • Unlikely (> 0–25%)
    • Somewhat likely (> 25–75%)
  • Very likely (> 75%)

Statistical Analysis

All analyses were performed using SAS® version 9.2 or higher (SAS Institute, Cary, NC, USA). Descriptive analyses corresponding to the specific research objectives were performed to characterize the GI analysis population. Continuous variables are reported as number of patients, mean, standard deviation (SD), median, minimum, and maximum where appropriate. Categorical variables are summarized as number of patients and percentage.
Data were summarized for (1) select GI events and GI events leading to DMF discontinuation overall and over time, (2) each GI management strategy as reported in the GI questionnaire, and (3) the site-level discontinuation rates according to counseling patterns.

Standard Protocol Approvals, Registrations, and Patient Consent

The protocol was approved by the relevant Institutional Review Board for each study site. All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. Informed consent was obtained from all individual participants included in the study. The study was conducted in accordance with the Declaration of Helsinki, International Conference on Harmonization—Good Clinical Practice, and all applicable laws and regulations. A waiver of informed consent, based on non-personally identifiable retrospective data collection and minimal risk, was at the discretion of the individual Institutional Review Boards or Ethics Committees for each site. When required, participants provided written informed consent before study enrollment.

Results

Patients and Sites

Overall, 826 DMF-treated patients were enrolled at 66 sites (Table 1), with patient recruitment per site ranging from 1 to 107 patients (median 7). Mean (SD) age was 44 (12) years; 76% (624/826) of patients were female; 57% (467/826) of patients were from the USA (Region 1); and 32% (265/826) were treatment naive. Of the patients with a prior MS treatment, 76% (393/515) had received IFN beta. A total of 14% (118/826) of patients discontinued treatment with DMF, most commonly due to tolerability issues [9% (71/826 patients)].
Table 1
Baseline characteristics and patient disposition
Characteristic
DMF-treated patients (n = 826)
Age, median (min, max), years
44 (18, 73)
Age, mean (SD), years
44 (12)
Female
624 (76)
Regiona
 Region 1
467 (57)
 Region 2
320 (39)
 Region 3
39 (5)
Any prior MS treatmentb
515 (63)
 IFN beta
393 (48)
 GA
115 (14)
 Otherc
7 (< 1)
Treatment naive
265 (32)
Reasons for discontinuing prior MS treatmentb,d,e
 Tolerability
244 (30)
 Efficacy
165 (20)
 Adverse events
14 (2)
 Patient preference
130 (16)
 Other
53 (6)
Discontinued DMF by 1 year, n (%)
118 (14)
Reasons for discontinuing DMFd
 Tolerability
71 (9)
 Efficacy
19 (2)
 Safety
16 (2)
 Patient preference
14 (2)
 Other
11 (1)
Values in table are presented as a number with the percentage in parenthesis, unless noted otherwise
DMF delayed-release dimethyl fumarate, GA glatiramer acetate, IFN interferon, max maximum, min minimum, MS multiple sclerosis
aRegion 1: USA; Region 2: Argentina, Australia, Canada, France, Germany, Italy, Spain, Switzerland, UK; Region 3: Croatia, Czech Republic, Hungary
bBased on 816 patients with data available
cFive patients previously used a chronic MS steroid, one patient received natalizumab, and one patient received rituximab
dMore than one reason for discontinuing prior MS treatment was permitted; data were collected retrospectively
eReasons for discontinuation were based on clinical judgement; no formal criteria were provided

GI Analysis

A total of 809 patients from 65 sites who completed the GI questionnaire were included in the GI analysis. In the first 12 months of treatment, 27% (216) of patients had at least one GI event recorded in their medical charts. The most commonly reported GI events were nausea [11% (87 patients)], diarrhea [9% (74)], abdominal pain [6% (51)], vomiting [5% (43)], upper abdominal pain [2% (20)], abdominal discomfort [2% (19)], and dyspepsia [2% (15)]. The majority (81%) of GI events occurred within the first 5 weeks of DMF treatment initiation (Fig. 1). However, only 5% (44 patients) discontinued DMF due to GI events, with nausea [3% (21)] being the most common event leading to discontinuation, followed by diarrhea [2% (19)], abdominal pain [2% (15)], and vomiting [2% (13)]. Similar to the onset of GI events, the majority of events leading to discontinuation occurred in the first 5 weeks of therapy (92%).
Titration schedules were recorded in the medical charts for 727/809 patients; data were missing for 82 patients. Approximately 50% (331/727) of patients titrated their DMF dose for 1 week, 20% (151/727) titrated it for 2–4 weeks, and < 10% (59/727) titrated it for > 4 weeks. No pattern of discontinuation was identified when the data were stratified by titration schedule. However, the number of patients with no titration schedule reported in their medical records (186/727) or with missing data impacted the evaluable sample size and the ability to interpret the data. Similarly, of the 216 patients with ≥ 1 GI event, only 4% received dosage modification and 11% received symptomatic therapy. Therefore, it was not possible to perform additional analyses due to the small number of evaluable patients.
Discontinuation rates due to GI events varied by region. Regions were defined on the basis of geography, as well as by type of healthcare system and access to health care in each country. Discontinuation rates were 7.1% (32/451) in Region 1 (USA), 3.4% (11/320) in Region 2 (Argentina, Australia, Canada, France, Germany, Italy, Spain, Switzerland, UK), and 2.6% (1/38) in Region 3 (Croatia, Czech Republic, Hungary).

Patient Management Strategies: Questionnaire Results

Respondent and Site Characteristics

Questionnaire respondents were physicians (48%), registered nurses (15%), nurse practitioners (14%), physician assistants (2%), and other (22%; included clinical research coordinators, research assistants, and study coordinators). Respondents characterized their site type as nonhospital-based community practice (45%), hospital-based community practice (28%), academic setting (18%), or other (9%). They characterized their practice size as ≤ 250 patients (25%), 251–500 patients (14%), 501–1000 patients (26%), or > 1000 patients (35%).

Site-Reported GI Management and Mitigation Practices

Most sites [86% (54/63)] were very likely to recommend that DMF be taken with food or that specific diets be followed, such as high fat, high protein, or high starch (Fig. 2a). Additionally, 48% (30/62) of sites were very likely to recommend the use of symptomatic therapies for GI AEs. The most frequently recommended symptomatic therapies included proton pump inhibitors, secretion blockers, and antidiarrheal medications (Fig. 2b).

Site-Reported Counseling Practices

Most sites [92% (58/63)] reported that patients were very likely to be counseled orally regarding GI events at or before the initiation of DMF treatment (Fig. 3), and 34% (22/64) of sites were very likely to utilize a member of the healthcare team, in addition to the prescriber, to counsel patients at or before DMF treatment initiation (Fig. 3). In the event the prescriber was unavailable to provide counseling at or before DMF treatment initiation, 19% (12/63) of sites were very likely to utilize another member of the healthcare team to counsel patients. The other HCPs providing counseling included registered nurses, physicians other than the prescribing physician, nurse practitioners, and physician assistants. Most sites [83% (52/63)] were very likely to provide patients with specific details of GI events (timing of onset, incidence, severity, and duration); 44% (28/64) of sites were very likely to provide patients with information about GI events in written form (handwritten, printed, emailed, and online), and 92% (59/64) of sites instructed patients to contact the office if they experienced GI events. Seventy-eight percent (49/63) of sites were very likely to advise patients to titrate the dose of DMF over the first week of treatment to prevent GI events, but only 41% (26/63) of sites were likely to advise patients to temporarily reduce the dose of DMF if the patient experienced GI events; only 26% (14/53) of sites were very likely to advise patients to temporarily reduce the dose of DMF to 120 mg twice daily, as per approved package labeling, if they experienced GI events; and only 13% (8/63) of sites were very likely to advise patients to temporarily interrupt the dose of DMF. Most sites [86% (54/63)] were very likely to recommend food as therapy; 48% (30/62) of sites were likely to recommend symptomatic therapy. Sites that were likely to counsel patients orally also were likely to indicate that written information was available [42% (27/65)], to recommend food [77% (50/65)], and to recommend concomitant symptomatic therapy [45% (29/65)].

Discontinuation Rates According to Counseling Patterns: Questionnaire Results

In a descriptive analysis, lower discontinuation rates were reported at sites that were very likely, versus sites that were not very likely, to have a member of the healthcare team provide counseling in addition to or in lieu of the prescribing physician, provide specific details about GI events, recommend taking DMF with food, and/or use symptomatic GI therapies (Fig. 4). Discontinuation rates were similar at sites that were very likely to provide counseling in the form of written information versus sites that were not very likely to do so (Fig. 4). The sites that utilized written information in their handouts included GI management strategies identified in the Delphi study (ESM Appendices S2 and S3).

Discussion

In this GI analysis of DMF-treated patients, the majority of GI AEs and GI-related discontinuations in this study occurred within the first month of treatment initiation, stressing the importance of preparing the patient for possible DMF-related GI events and the need for early intervention. Similarly to the single-arm studies MANAGE and TOLERATE, the incidence of GI events was highest in the first month of DMF treatment [8, 18]. Unfortunately, due to the retrospective nature of this study, based on data collection via chart abstraction, we were not able to determine the prevalence or duration of AEs because recurrent events may not have been captured and AE “stop dates” are frequently not reported in medical charts or listed as unknown. A future prospective clinical trial in which prevalence and duration of AEs are analyzed would be informative.
The incidence of GI AEs (27%) and the proportion of patients discontinuing treatment as a result of GI AEs (5%) in our analysis was somewhat lower than has been reported in other real-world studies, but similar to what was observed in controlled clinical trials [4, 6, 11]. The data from the site survey responses indicate a high likelihood that the patients in this study were counseled about GI symptoms associated with DMF treatment. It is hypothesized that the implementation of GI management and mitigation strategies mimics the clinical trial experience for the patient and is improving as experience in the use of DMF increases. DMF was approved for use by the US Food and Drug Administration in March 2013, followed by the European Medicines Agency in January 2014. Thus, of the patient charts abstracted for this study, more patients initiated DMF during the period 2014–2015 [65% (528/809)] versus previous years [35% (281/809)]. There were fewer discontinuations due to GI AEs among patients initiating DMF treatment in the latter half of the recruitment period versus the initial half of the recruitment period [4.2% (22/528) vs. 7.8% (22/281)], which supports the hypothesis that experience with DMF is resulting in improved practice management over time. Another explanation for the lower number of discontinuations due to GI AEs in our analysis compared to those reported in other real-world analyses [8, 12, 13], which may also relate to the timing of DMF initiation, is that the majority of patients enrolled in this study initiated therapy during the latter half of the study when prescribers had a better understanding of how to manage patients with GI events using tools like the Delphi consensus paper as references [10]. In general, sites that were more likely to frequently utilize these strategies had lower rates of discontinuation due to GI AEs in this study, although only discontinuation rates, not adherence to treatment, were specifically assessed. Overall discontinuation rate was utilized as a surrogate for adherence to treatment, which does not necessarily mean the patient received the full dose; for example, treatment could have decreased to one dose per day to enable the patient to better tolerate the GI effects. Dose modifications were not measured in this study, but they are an important variable to assess in future research. Finally, another inherent limitation of this study, due to its design, is the possibility of under-reporting of events collected in this study, as the data are reliant upon accuracy of the medical charts.
Lower discontinuation rates were observed at sites that were very likely, versus sites that were not very likely, to have an HCP, in addition to or in lieu of the prescriber, counseling patients, providing specific details about GI events, recommending taking DMF with food, or recommending using symptomatic therapy. Therefore, providing this type of specific guidance to patients may be most helpful to reducing discontinuations due to GI events. Of note, only a small percentage of patients were recorded actually using symptomatic therapy or having a modified dose titration schedule in the patient-level chart data. Due to inherent limitations in the study design, this value may be under-reported because the majority of symptomatic therapies are over-the-counter therapies or because dose titration instructions may have been given verbally to some patients and not recorded in the medical chart data. Additionally, this study did not demonstrate that use of written information as a counseling strategy was effective at reducing site-level discontinuation rates. It is speculated that written counseling may have been offered instead of (rather than a supplement to) oral counseling. Other studies have shown written forms of counseling may be an effective part of the DMF GI management strategy [15, 19].
The EFFECT study observed varying discontinuation rates among the different regions. Potential reasons for the observed variations in discontinuation rates include differences in regional practices of implementing GI management strategies and variation in years of experience in prescribing DMF. As part of a post hoc analysis, it was observed that the incidence of GI adverse events in Region 1 [29% (129/451)] versus combined Region 2/3 [24% (87/358)] were similar in this study, yet discontinuation rates were strikingly different in Region 1 [7% (32/451)] versus combined Region 2/3 [3% (12/358)]. Consistent with the analysis for the entire population, similar patterns of lower discontinuation rates for patients initiating therapy in more recent years were also observed when stratified by region. One hypothesis for the difference in discontinuation rates despite a similar incidence of AEs is that the management and mitigation strategies implemented by these regions drive the differences in discontinuations due to GI AEs associated with DMF treatment. Another hypothesis is that limited access to a wider range of MS treatment alternatives in particular countries may result in lower discontinuation rates irrespective of side effects. Other inherent country differences that may influence patient tolerability to DMF and willingness to tolerate side effects, such as diet, availability of over-the-counter symptomatic therapies, exercise, meal timing, and cultural norms that discourage the reporting of side effects, should be noted as well, as supported by other real-world studies from several countries that have reported differences in overall and GI-related discontinuation rates [12, 13, 18, 20].
In summary, DMF is efficacious for the treatment of RRMS, and oral administration is a convenient dosing form for patients. However, for patients to optimize the efficacy benefits of DMF they must overcome potential initial tolerability hurdles, including DMF-related GI AEs. GI counseling and management strategies implemented early in the treatment course may be critically important in driving patients to reach this goal.

Conclusions

The results of this study suggest that the use of a variety of GI counseling and management strategies may improve persistence on DMF therapy and increase the likelihood that patients can optimize the efficacy benefits of long-term DMF treatment.

Acknowledgements

The authors wish to thank the patients who participated in this study, which allowed this research to be possible.

Funding

This study was sponsored by Biogen (Cambridge, MA, USA). All authors had full access to all of the data in this study and take complete responsibility for the integrity of the data and accuracy of the data analysis. Biogen funded the article processing charges.

Medical Writing, Editorial, and Other Assistance

Writing and editorial support for the preparation of this manuscript was provided by Excel Scientific Solutions (Southport, CT, USA). Funding was provided by Biogen.

Authorship

All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published.

Disclosures

Jinny Min was a contractor for Biogen at the time of study analysis and is currently an employee of Rhythm Pharmaceuticals. Stanley Cohan has received consulting fees from advisory boards and from steering committees for Biogen, Genzyme, and Novartis; speaker fees from Acorda, Biogen, Genentech-Roche, Novartis, and Sanofi-Genzyme; research grants from Biogen, Genentech-Roche, MedDay, Novartis, and Sanofi-Genzyme, and speakers bureau for Biogen, Genentech-Roche, and Sanofi-Genzyme. Enrique Alvarez has received consulting fees from Actelion, Biogen, Celgene, EMD Serono, Genentech, Genzyme, Novartis, and TG Pharmaceuticals; research funding from Acorda, Biogen, Genentech, Novartis, and the Rocky Mountain MS Center. Jacob Sloane has received consulting fees from Biogen, Genentech, Genzyme, and Teva; research grants from Biogen and Genzyme. J. Theodore Phillips has received consulting or speaking fees from Acorda, Biogen, Genzyme, and TG Pharmaceuticals. Anneke van der Walt has received consulting fees from advisory boards for Genzyme, Merck, and Novartis; travel honoraria from Biogen, Merck, Novartis, and Teva. Fang Fang is an employee of Cytel Inc. Irene Koulinska is an employee of and holds stock/stock options in Biogen. Catherine Miller is an employee of and holds stock/stock options in Biogen. Andrew Chan has received compensation for activities with Actelion, Almirall, Bayer HealthCare, Biogen, Celgene, Genzyme, Merck, Novartis, Roche, Sanofi-Aventis, and Teva Neuroscience, all for university research funds; research support from Biogen, Genzyme, and UCB.

Compliance with Ethics Guidelines

The protocol was approved by the relevant Institutional Review Board for each study site. All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. Informed consent was obtained from all individual participants included in the study. The study was conducted in accordance with the Declaration of Helsinki, International Conference on Harmonization—Good Clinical Practice, and all applicable laws and regulations. A waiver of informed consent, based on non-personally identifiable retrospective data collection and minimal risk, was at the discretion of the individual Institutional Review Boards or Ethics Committees for each site. When required, participants provided written informed consent before study enrollment.

Data Availability

The datasets used and/or analyzed during the current study are available from the corresponding author upon reasonable request.

Open Access

This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://​creativecommons.​org/​licenses/​by-nc/​4.​0/​), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
Anhänge

Electronic supplementary material

Below is the link to the electronic supplementary material.
Literatur
1.
Zurück zum Zitat Giannetti P, Niccolini NR. BG-12 and its potential for the prevention of relapse in multiple sclerosis. Degener Neurol Neuromuscul Dis. 2012;10:119. Giannetti P, Niccolini NR. BG-12 and its potential for the prevention of relapse in multiple sclerosis. Degener Neurol Neuromuscul Dis. 2012;10:119.
2.
Zurück zum Zitat Edwards KRPN, Rogge M, Sheikh S, Zhu B. A pharmacokinetic study of delayed-release dimethyl fumarate to evaluate cerebrospinal fluid penetration in patients with secondary progressive multiple sclerosis. Mult Scler. 2016;22[Supp 3]:784–5. Edwards KRPN, Rogge M, Sheikh S, Zhu B. A pharmacokinetic study of delayed-release dimethyl fumarate to evaluate cerebrospinal fluid penetration in patients with secondary progressive multiple sclerosis. Mult Scler. 2016;22[Supp 3]:784–5.
3.
Zurück zum Zitat Brennan MS, Matos MF, Li B, et al. Dimethyl fumarate and monoethyl fumarate exhibit differential effects on KEAP1, NRF2 activation, and glutathione depletion in vitro. PLoS One. 2015;10(3):e0120254.CrossRef Brennan MS, Matos MF, Li B, et al. Dimethyl fumarate and monoethyl fumarate exhibit differential effects on KEAP1, NRF2 activation, and glutathione depletion in vitro. PLoS One. 2015;10(3):e0120254.CrossRef
4.
Zurück zum Zitat Fox RJ, Miller DH, Phillips JT, et al. Placebo-controlled phase 3 study of oral BG-12 or glatiramer in multiple sclerosis. N Engl J Med. 2012;367(12):1087–97.CrossRef Fox RJ, Miller DH, Phillips JT, et al. Placebo-controlled phase 3 study of oral BG-12 or glatiramer in multiple sclerosis. N Engl J Med. 2012;367(12):1087–97.CrossRef
5.
Zurück zum Zitat Gold R, Arnold DL, Bar-Or A, et al. Long-term effects of delayed-release dimethyl fumarate in multiple sclerosis: interim analysis of ENDORSE, a randomized extension study. Mult Scler. 2017;23(2):253–65.CrossRef Gold R, Arnold DL, Bar-Or A, et al. Long-term effects of delayed-release dimethyl fumarate in multiple sclerosis: interim analysis of ENDORSE, a randomized extension study. Mult Scler. 2017;23(2):253–65.CrossRef
6.
Zurück zum Zitat Gold R, Kappos L, Arnold DL, et al. Placebo-controlled phase 3 study of oral BG-12 for relapsing multiple sclerosis. N Engl J Med. 2012;367(12):1098–107.CrossRef Gold R, Kappos L, Arnold DL, et al. Placebo-controlled phase 3 study of oral BG-12 for relapsing multiple sclerosis. N Engl J Med. 2012;367(12):1098–107.CrossRef
7.
Zurück zum Zitat Phillips JT, Selmaj K, Gold R, et al. Clinical significance of gastrointestinal and flushing events in patients with multiple sclerosis treated with delayed-release dimethyl fumarate. Int J MS Care. 2015;17(5):236–43.CrossRef Phillips JT, Selmaj K, Gold R, et al. Clinical significance of gastrointestinal and flushing events in patients with multiple sclerosis treated with delayed-release dimethyl fumarate. Int J MS Care. 2015;17(5):236–43.CrossRef
8.
Zurück zum Zitat Fox EJ, Vasquez A, Grainger W, et al. Gastrointestinal tolerability of delayed-release dimethyl fumarate in a multicenter, open-label study of patients with relapsing forms of multiple sclerosis (MANAGE). Int J MS Care. 2016;18(1):9–18.CrossRef Fox EJ, Vasquez A, Grainger W, et al. Gastrointestinal tolerability of delayed-release dimethyl fumarate in a multicenter, open-label study of patients with relapsing forms of multiple sclerosis (MANAGE). Int J MS Care. 2016;18(1):9–18.CrossRef
9.
Zurück zum Zitat Livingston T, Fay M, Iyer R, Wells W, Pill MW. Quantifying differences in health care consumption for the management of multiple sclerosis within privately and publicly insured health care programs. J Manag Care Spec Pharm. 2016;22(12):1385–91.PubMed Livingston T, Fay M, Iyer R, Wells W, Pill MW. Quantifying differences in health care consumption for the management of multiple sclerosis within privately and publicly insured health care programs. J Manag Care Spec Pharm. 2016;22(12):1385–91.PubMed
10.
Zurück zum Zitat Phillips JT, Erwin AA, Agrella S, et al. Consensus management of gastrointestinal events associated with delayed-release dimethyl fumarate: a Delphi study. Neurol Ther. 2015;4(2):137–46.CrossRef Phillips JT, Erwin AA, Agrella S, et al. Consensus management of gastrointestinal events associated with delayed-release dimethyl fumarate: a Delphi study. Neurol Ther. 2015;4(2):137–46.CrossRef
11.
Zurück zum Zitat Phillips J, Agrella S, Fox RJ. Dimethyl fumarate: a review of efficacy and practical management strategies for common adverse events in patients with multiple sclerosis. Int J MS Care. 2017;19(2):74–83.CrossRef Phillips J, Agrella S, Fox RJ. Dimethyl fumarate: a review of efficacy and practical management strategies for common adverse events in patients with multiple sclerosis. Int J MS Care. 2017;19(2):74–83.CrossRef
12.
Zurück zum Zitat Ontaneda D, Vollmer B, Sillau S, et al. Comparative efficacy and discontinuation of fingolimod and dimethyl fumarate in two large academic medical centers. Neurology. 2016;86[Suppl 16]:P3.109. Ontaneda D, Vollmer B, Sillau S, et al. Comparative efficacy and discontinuation of fingolimod and dimethyl fumarate in two large academic medical centers. Neurology. 2016;86[Suppl 16]:P3.109.
13.
Zurück zum Zitat Vu N, Bradshaw M, Moses H, Sriram S, Pawate S. Efficacy and tolerability of fingolimod, dimethyl fumarate, and teriflunomide in patients with multiple sclerosis: real world experience from a single center. Neurology. 2016;86[Suppl 16]:P6168. Vu N, Bradshaw M, Moses H, Sriram S, Pawate S. Efficacy and tolerability of fingolimod, dimethyl fumarate, and teriflunomide in patients with multiple sclerosis: real world experience from a single center. Neurology. 2016;86[Suppl 16]:P6168.
14.
Zurück zum Zitat Biogen. Data on file. Biogen: Cambridge, MA Biogen. Data on file. Biogen: Cambridge, MA
15.
Zurück zum Zitat Begus-Nahrmann Y, Niemczyk G, Schmid B, Mäurer M. The potential of individualized patient coaching to optimize treatment with delayed-release dimethyl fumarate: a retrospective analysis of patients with multiple sclerosis treated in a real-world setting. Mult Scler. 2016;22[Suppl 3]:636. Begus-Nahrmann Y, Niemczyk G, Schmid B, Mäurer M. The potential of individualized patient coaching to optimize treatment with delayed-release dimethyl fumarate: a retrospective analysis of patients with multiple sclerosis treated in a real-world setting. Mult Scler. 2016;22[Suppl 3]:636.
17.
Zurück zum Zitat Polman CH, Reingold SC, Banwell B, et al. Diagnostic criteria for multiple sclerosis: 2010 revisions to the McDonald criteria. Ann Neurol. 2011;69(2):292–302.CrossRef Polman CH, Reingold SC, Banwell B, et al. Diagnostic criteria for multiple sclerosis: 2010 revisions to the McDonald criteria. Ann Neurol. 2011;69(2):292–302.CrossRef
18.
Zurück zum Zitat Gold R, Schlegel E, Elias-Hamp B, et al. Incidence and mitigation of gastrointestinal events in patients with relapsing-remitting Multiple Sclerosis receiving delayed-release dimethyl fumarate—a German phase IV study (TOLERATE). Ther Adv Neurol Disord. 2018;11:1756286418768775.CrossRef Gold R, Schlegel E, Elias-Hamp B, et al. Incidence and mitigation of gastrointestinal events in patients with relapsing-remitting Multiple Sclerosis receiving delayed-release dimethyl fumarate—a German phase IV study (TOLERATE). Ther Adv Neurol Disord. 2018;11:1756286418768775.CrossRef
19.
Zurück zum Zitat Sammarco C, Laing L, Minetti J, Desanctis C, Herbert J. Strategies to reduce adverse events related to oral dimethyl fumarate. Mult Scler. 2014;20[Suppl 1]:206. Sammarco C, Laing L, Minetti J, Desanctis C, Herbert J. Strategies to reduce adverse events related to oral dimethyl fumarate. Mult Scler. 2014;20[Suppl 1]:206.
20.
Zurück zum Zitat Vorobeychik G, Potts J, Smith M, Vlaicu M. A retrospective analysis of discontinuation rates and reasons for discontinuation in multiple sclerosis patients treated with delayed-release dimethyl fumarate (Biogen ONE Support Program). Mult Scler. 2016;22[Suppl 3]:301–2. Vorobeychik G, Potts J, Smith M, Vlaicu M. A retrospective analysis of discontinuation rates and reasons for discontinuation in multiple sclerosis patients treated with delayed-release dimethyl fumarate (Biogen ONE Support Program). Mult Scler. 2016;22[Suppl 3]:301–2.
Metadaten
Titel
Real-World Characterization of Dimethyl Fumarate-Related Gastrointestinal Events in Multiple Sclerosis: Management Strategies to Improve Persistence on Treatment and Patient Outcomes
verfasst von
Jinny Min
Stanley Cohan
Enrique Alvarez
Jacob Sloane
J. Theodore Phillips
Anneke van der Walt
Irene Koulinska
Fang Fang
Catherine Miller
Andrew Chan
Publikationsdatum
31.01.2019
Verlag
Springer Healthcare
Erschienen in
Neurology and Therapy / Ausgabe 1/2019
Print ISSN: 2193-8253
Elektronische ISSN: 2193-6536
DOI
https://doi.org/10.1007/s40120-019-0127-2

Weitere Artikel der Ausgabe 1/2019

Neurology and Therapy 1/2019 Zur Ausgabe

Leitlinien kompakt für die Neurologie

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Schützt Olivenöl vor dem Tod durch Demenz?

10.05.2024 Morbus Alzheimer Nachrichten

Konsumieren Menschen täglich 7 Gramm Olivenöl, ist ihr Risiko, an einer Demenz zu sterben, um mehr als ein Vierten reduziert – und dies weitgehend unabhängig von ihrer sonstigen Ernährung. Dafür sprechen Auswertungen zweier großer US-Studien.

Bluttest erkennt Parkinson schon zehn Jahre vor der Diagnose

10.05.2024 Parkinson-Krankheit Nachrichten

Ein Bluttest kann abnorm aggregiertes Alpha-Synuclein bei einigen Menschen schon zehn Jahre vor Beginn der motorischen Parkinsonsymptome nachweisen. Mit einem solchen Test lassen sich möglicherweise Prodromalstadien erfassen und die Betroffenen früher behandeln.

Darf man die Behandlung eines Neonazis ablehnen?

08.05.2024 Gesellschaft Nachrichten

In einer Leseranfrage in der Zeitschrift Journal of the American Academy of Dermatology möchte ein anonymer Dermatologe bzw. eine anonyme Dermatologin wissen, ob er oder sie einen Patienten behandeln muss, der eine rassistische Tätowierung trägt.

Wartezeit nicht kürzer, aber Arbeit flexibler

Psychotherapie Medizin aktuell

Fünf Jahren nach der Neugestaltung der Psychotherapie-Richtlinie wurden jetzt die Effekte der vorgenommenen Änderungen ausgewertet. Das Hauptziel der Novellierung war eine kürzere Wartezeit auf Therapieplätze. Dieses Ziel wurde nicht erreicht, es gab jedoch positive Auswirkungen auf andere Bereiche.

Update Neurologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.