Cladribine Tablets and Relapsing-Remitting Multiple Sclerosis: A Pragmatic, Narrative Review of What Physicians Need to Know.

Cladribine tablets Disease-modifying drugs Immune reconstitution therapy Relapsing–remitting multiple sclerosis

Journal

Neurology and therapy
ISSN: 2193-8253
Titre abrégé: Neurol Ther
Pays: New Zealand
ID NLM: 101637818

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 25 11 2019
pubmed: 15 2 2020
medline: 15 2 2020
entrez: 15 2 2020
Statut: ppublish

Résumé

Immune reconstitution therapy (IRT) is an emerging management concept for multiple sclerosis, whereby a short course of treatment provides long-lasting suppression of disease activity. "Cladribine tablets 10 mg" refers to a total cumulative dose of cladribine given over 2 years (henceforth referred to as cladribine tablets 3.5 mg/kg); it is a relatively new treatment option that is hypothesised to act as an IRT acting preferentially on the adaptive immune system. A randomised, 2-year, placebo-controlled trial (CLARITY) showed that treatment with cladribine tablets reduced indices of disease activity (relapses, lesions on magnetic resonance images, disability progression) and that this effect outlasted the pharmacologic effect of the treatment on the immune system (mainly a reduction in circulating B and T cells, with little effect on components of the innate immune system such as monocytes). CLARITY Extension, a 2-year extension to this trial, demonstrated durable efficacy, also in patients who received the standard 2-year course of cladribine tablets 3.5 mg/kg and were re-randomised to placebo for a further 2 years. Relative risk reductions for relapse rate with cladribine tablets 3.5 mg/kg were similar for patients with or without prior high disease activity. Reductions in disability progression with cladribine tablets 3.5 mg/kg were higher in patients with prior high relapse rates with or without prior treatment non-response. In this review, we describe the therapeutic profile of cladribine tablets 3.5 mg/kg and provide practical information on initiating this treatment option in the most appropriate patients.

Identifiants

pubmed: 32056129
doi: 10.1007/s40120-020-00177-5
pii: 10.1007/s40120-020-00177-5
pmc: PMC7229040
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

11-23

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Auteurs

Mohamed AlJumah (M)

King Fahad Medical City, Ministry of Health, Riyadh, Kingdom of Saudi Arabia. jumahm@gmail.com.

Mona Marwan Alkhawajah (MM)

King Faisal Specialist Hospital and Research Center, Riyadh, Kingdom of Saudi Arabia.

Shireen Qureshi (S)

Johns Hopkins Aramco Healthcare, Dhahran, Kingdom of Saudi Arabia.

Ibtisam Al-Thubaiti (I)

King Fahad Military Medical Complex, Dhahran, Kingdom of Saudi Arabia.

Omar Ayoub (O)

King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.

Saeed A Bohlega (SA)

King Faisal Specialist Hospital and Research Center, Riyadh, Kingdom of Saudi Arabia.

Areej Bushnag (A)

International Medical Center, Jeddah, Kingdom of Saudi Arabia.

Edward Cupler (E)

King Faisal Specialist Hospital and Research Center, Jeddah, Kingdom of Saudi Arabia.

Abdulkader Daif (A)

King Khaled University Hospital, Riyadh, Kingdom of Saudi Arabia.

Ahmed El Boghdady (A)

Merck KGaA, Darmstadt, Germany.

Ahmed Hassan (A)

King Faisal Specialist Hospital and Research Center, Jeddah, Kingdom of Saudi Arabia.

Yaser Al Malik (Y)

King Saud Bin Abdulaziz University for Health Sciences (KSBU-HS), King Abdulaziz Medical City, Riyadh, Kingdom of Saudi Arabia.

Jameelah Saeedi (J)

King Abdullah Bin Abdulaziz University Hospital, KAAUH, Riyadh, Kingdom of Saudi Arabia.

Fawzia Al-Shamrany (F)

Imam Abdulrahman Bin Faisal University, Riyadh, Kingdom of Saudi Arabia.

Eslam Shosha (E)

King Khaled Hospital, Al-Majmaah, Kingdom of Saudi Arabia.

Peter Rieckmann (P)

Bamberg Hospital and University of Erlangen, Bamberg, Germany.

Classifications MeSH