Nabiximols is an effective treatment for spasticity in MS. However, treatment discontinuation over-time might occur and predictors of sustained treatment persistence over long-term follow-up in real-world settings are highly needed. We aim at evaluating baseline predictors of treatment persistence on Nabiximols. This is a retrospective real-world study including MS patients treated with Nabiximols. At baseline (Nabiximols prescription), we evaluated disability using the EDSS, and cognitive function using the Brief International Cognitive Assessment for Multiple Sclerosis (BICAMS). Nabiximols discontinuation was evaluated after 4 weeks of treatment ("titration phase''), and over the follow-up ("treatment phase"). We included 396 MS patients (228 females and 168 males). After 4 weeks (titration phase), 266 MS patients (67.2%) were considered persistent on treatment, while 130 patients dropped out. After 19 ± 21 months (treatment phase), 136 out of 266 MS patients (51.1%) were still on treatment, whereas 130 patients dropped at follow-up. Higher EDSS and cognitive impairment predicted treatment discontinuation at follow-up (p = 0.04 and p = 0.005, respectively). In conclusion, higher physical and cognitive disability predicted Nabiximols treatment discontinuation over 2 years in MS patients suffering from spasticity. Nabiximols should be started earlier to decrease the likelihood of treatment discontinuation over time.

Predictors of Nabiximols (Sativex®) discontinuation over long-term follow-up: a real-life study / Carotenuto, Antonio; Costabile, Teresa; De Lucia, Mario; Moccia, Marcello; Falco, Fabrizia; Petruzzo, Martina; De Angelis, Marcello; Russo, Cinzia Valeria; Saccà, Francesco; Lanzillo, Roberta; Brescia Morra, Vincenzo. - In: JOURNAL OF NEUROLOGY. - ISSN 0340-5354. - (2020). [10.1007/s00415-020-09739-x]

Predictors of Nabiximols (Sativex®) discontinuation over long-term follow-up: a real-life study

Carotenuto, Antonio;Costabile, Teresa;Moccia, Marcello;Falco, Fabrizia;Petruzzo, Martina;De Angelis, Marcello;Russo, Cinzia Valeria;Saccà, Francesco;Lanzillo, Roberta;Brescia Morra, Vincenzo
2020

Abstract

Nabiximols is an effective treatment for spasticity in MS. However, treatment discontinuation over-time might occur and predictors of sustained treatment persistence over long-term follow-up in real-world settings are highly needed. We aim at evaluating baseline predictors of treatment persistence on Nabiximols. This is a retrospective real-world study including MS patients treated with Nabiximols. At baseline (Nabiximols prescription), we evaluated disability using the EDSS, and cognitive function using the Brief International Cognitive Assessment for Multiple Sclerosis (BICAMS). Nabiximols discontinuation was evaluated after 4 weeks of treatment ("titration phase''), and over the follow-up ("treatment phase"). We included 396 MS patients (228 females and 168 males). After 4 weeks (titration phase), 266 MS patients (67.2%) were considered persistent on treatment, while 130 patients dropped out. After 19 ± 21 months (treatment phase), 136 out of 266 MS patients (51.1%) were still on treatment, whereas 130 patients dropped at follow-up. Higher EDSS and cognitive impairment predicted treatment discontinuation at follow-up (p = 0.04 and p = 0.005, respectively). In conclusion, higher physical and cognitive disability predicted Nabiximols treatment discontinuation over 2 years in MS patients suffering from spasticity. Nabiximols should be started earlier to decrease the likelihood of treatment discontinuation over time.
2020
Predictors of Nabiximols (Sativex®) discontinuation over long-term follow-up: a real-life study / Carotenuto, Antonio; Costabile, Teresa; De Lucia, Mario; Moccia, Marcello; Falco, Fabrizia; Petruzzo, Martina; De Angelis, Marcello; Russo, Cinzia Valeria; Saccà, Francesco; Lanzillo, Roberta; Brescia Morra, Vincenzo. - In: JOURNAL OF NEUROLOGY. - ISSN 0340-5354. - (2020). [10.1007/s00415-020-09739-x]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/804419
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