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| Return to: GILENYA (fingolimod, FTY720) | |
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| #Post#: 1794-------------------------------------------------- | |
| (Abst.) Switching from Tysabri to Gilenya within 6 weeks cuts re | |
| currence of MS disease activity | |
| By: agate Date: August 22, 2017, 9:52 am | |
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| From PubMed, August 22, 2017: | |
| [quote]Mult Scler. 2017 Aug 1:1352458517726381. | |
| Switching natalizumab to fingolimod within 6 weeks reduces | |
| recurrence of disease activity in MS patients | |
| Leurs CE1, van Kempen ZL1, Dekker I2, Balk LJ1, Wattjes MP3, | |
| Rispens T4, Uitdehaag BM1, Killestein J1. | |
| Author information | |
| 1 | |
| Department of Neurology, Neuroscience Amsterdam, VUmc MS Center | |
| Amsterdam, VU University Medical Center, Amsterdam, The | |
| Netherlands. | |
| 2 | |
| Department of Neurology, Neuroscience Amsterdam, VUmc MS Center | |
| Amsterdam, VU University Medical Center, Amsterdam, The | |
| Netherlands / Department of Radiology and Nuclear Medicine, | |
| Neuroscience Amsterdam, VUmc MS Center Amsterdam, VU University | |
| Medical Center, Amsterdam, The Netherlands. | |
| 3 | |
| Department of Radiology and Nuclear Medicine, Neuroscience | |
| Amsterdam, VUmc MS Center Amsterdam, VU University Medical | |
| Center, Amsterdam, The Netherlands. | |
| 4 | |
| Department of Immunology, Landsteiner Laboratory Sanquin | |
| Research, Amsterdam, The Netherlands. | |
| BACKGROUND: | |
| Natalizumab is an effective treatment in relapsing-remitting | |
| multiple sclerosis (MS). Mainly because of the risk of | |
| progressive multifocal leukoencephalopathy (PML), a substantial | |
| proportion of John Cunningham (JC) virus-positive patients | |
| switch to fingolimod. Previous reports show a clear benefit when | |
| the duration of a washout (WO) period of natalizumab is | |
| 0-3 months in comparison to longer WO periods. However, | |
| there is no consensus regarding the optimal duration of a WO | |
| period under 3 months. | |
| OBJECTIVE: | |
| We compared MS disease activity after different WO periods. In | |
| addition, we investigated several factors that possibly | |
| influence recurrence of disease activity, including serum | |
| natalizumab concentration and lymphocyte counts. | |
| METHODS: | |
| From a prospective observational cohort study of | |
| natalizumab-treated patients, we selected 52 patients who | |
| switched to fingolimod. We divided the patients in three groups | |
| (<6 weeks, 6-8 weeks, >8 weeks WO). Serum | |
| natalizumab concentration and lymphocyte count were assessed | |
| during and after natalizumab treatment. | |
| RESULTS: | |
| Patients with a WO period of >8 weeks had a significant | |
| higher recurrence of disease activity (odds ratio, 6.8; 95% | |
| confidence interval, 1.4-32.8) compared to patients with a WO | |
| period of <6 weeks. Serum natalizumab concentration and | |
| lymphocyte count did not predict recurrence of disease activity. | |
| INTERPRETATION: | |
| A short WO period decreases the risk of recurrence of disease | |
| activity. The possible impact of a short WO period on the risk | |
| of carry-over PML in JC virus-positive patients remains | |
| uncertain.[/quote] | |
| The abstract can be seen here | |
| https://www.ncbi.nlm.nih.gov/pubmed/28823223. | |
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