Multiple Sklerose
Studienlage · Detail Kohortenstudie · Multiple Sklerose · 2016

Long-Term Data of Efficacy, Safety, and Tolerability in a Real-Life Setting of THC/CBD Oromucosal Spray-Treated Multiple Sclerosis Patients.

Klarer Nutzen GRADE Niedrig 22 Zitate
Stichproben = 102 Pat.
Dauer40 Wochen
EndpunktNRS
Verblindungn.a.
DesignKohortenstudie
Cannabinoidkombination
THC:CBD1:1
Applikationoromukosal
Kernaussage

Signifikante Reduktion der Spastizität (NRS-Score um 2,5 ± 1,2 Punkte, P < 0,0001) sowie Verbesserung von Schmerz und Blasenfunktion.

Zusammenfassung

Real-World-Daten n=102 MS-Patienten mit THC/CBD-Spray über 40 Wochen; mittlere Tagesdosis 6,5±1,6 Sprühstöße. NRS-Spastizität sank um 2,5±1,2 Punkte (p<0,0001). Zusatzeffekte: NRS-Schmerzreduktion (n=58, p=0,011) und IPSS-Blasenfunktions-Verbesserung (n=46, p=0,001). Adverse Events 40,2%, Abbruchrate 36,2%.

P
PopulationErwachsene mit Multipler Sklerose und Spastik, n=102, italienische Postmarketing-Kohorte
I
InterventionTHC/CBD oromukosales Spray, durchschnittlich 6,5 ± 1,6 Sprühstöße/Tag als Add-on-Therapie
O
OutcomeMittlere NRS-Spastik-Reduktion um 2,5 ± 1,2 Punkte (p<0,0001); signifikante Verbesserung für Schmerz (p=0,011) und Blasendysfunktion/IPSS (p=0,001); 36,2% Therapieabbrüche; AE-Inzidenz 40,2%
Vertrauen in die Evidenz
Niedrig

Zweite von vier GRADE-Stufen, die Effektschätzung ist begrenzt verlässlich.

Qualitätsprofil
Größe
Verblindung
Effektstärke Klarer Nutzen
Zitate / Jahr
Autoren
Paolicelli D, Direnzo V, Manni A, D'Onghia M, Tortorella C, Zoccolella S, Di Lecce V, Iaffaldano A, Trojano M
DOI 10.1002/jcph.670
Design: Kohortenstudie
Teilen
Abstract
Delta-9-tetrahydrocannabinol (THC)/cannabidiol (CBD) oromucosal spray was approved as add-on therapy for spasticity in patients with multiple sclerosis (MS). We show our 40-week postmarketing experience regarding efficacy and safety of THC/CBD spray in an Italian cohort of 102 MS patients. Patients were evaluated using the Expanded Disability Status Scale (EDSS) score, the Numerical Rating Scale (NRS) for spasticity, the Ambulation Index (AI), and Timed 25-Foot Walk (T25-FW) at the beginning of treatment and then every 3 months. After 4 weeks, if a clinically significant improvement in spasticity (at least 20% of baseline NRS score) was not seen, administration of the drug was stopped. In our cohort, patients received an average of 6.5 +/- 1.6 sprays each day. The mean reduction to the NRS spasticity score was 2.5 +/- 1.2 points (P < .0001). Thirty-seven patients (36.2%) discontinued the treatment. The incidence of adverse events (AEs) was 40.2%. Fifty-eight patients (56.9%) were also assessed using the NRS for pain, and 46 patients (45.1%) with bladder dysfunction were assessed for the IPSS (International Prostatic Symptoms Score) score, showing a significant improvement in these scales (P = .011 and P = .001, respectively). In conclusion, treatment with THC/CBD spray appears to be a valid answer to some of the unmet needs in MS patients, such as spasticity and other refractory-to-treatment symptoms.

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