Evidence map›Paper›PMID 32056129›Full record

ReviewNeurology and therapy2020

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

Mohamed AlJumah, Mona Marwan Alkhawajah, Shireen Qureshi, Ibtisam Al-Thubaiti, Omar Ayoub, Saeed A Bohlega, Areej Bushnag, Edward Cupler, Abdulkader Daif, Ahmed El Boghdady and 6 more

Abstract readReview
In one paragraph

Review in Neurology and therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Article
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  4. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Mohamed AlJumahKing Fahad Medical City, Ministry of Health, Riyadh, Kingdom of Saudi Arabia. jumahm@gmail.com.
Mona Marwan AlkhawajahKing Faisal Specialist Hospital and Research Center, Riyadh, Kingdom of Saudi Arabia.
Shireen QureshiJohns Hopkins Aramco Healthcare, Dhahran, Kingdom of Saudi Arabia.
Ibtisam Al-ThubaitiKing Fahad Military Medical Complex, Dhahran, Kingdom of Saudi Arabia.
Omar AyoubKing Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.
Saeed A BohlegaKing Faisal Specialist Hospital and Research Center, Riyadh, Kingdom of Saudi Arabia.
Areej BushnagInternational Medical Center, Jeddah, Kingdom of Saudi Arabia.
Edward CuplerKing Faisal Specialist Hospital and Research Center, Jeddah, Kingdom of Saudi Arabia.
Abdulkader DaifKing Khaled University Hospital, Riyadh, Kingdom of Saudi Arabia.
Ahmed El BoghdadyMerck KGaA, Darmstadt, Germany.
Ahmed HassanKing Faisal Specialist Hospital and Research Center, Jeddah, Kingdom of Saudi Arabia.
Yaser Al MalikKing Saud Bin Abdulaziz University for Health Sciences (KSBU-HS), King Abdulaziz Medical City, Riyadh, Kingdom of Saudi Arabia.
Jameelah SaeediKing Abdullah Bin Abdulaziz University Hospital, KAAUH, Riyadh, Kingdom of Saudi Arabia.
Fawzia Al-ShamranyImam Abdulrahman Bin Faisal University, Riyadh, Kingdom of Saudi Arabia.
Eslam ShoshaKing Khaled Hospital, Al-Majmaah, Kingdom of Saudi Arabia.
Peter RieckmannBamberg Hospital and University of Erlangen, Bamberg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Cladribine tabletsDisease-modifying drugsImmune reconstitution therapyRelapsing–remitting multiple sclerosis

Identifiers

PMID32056129
PMCPMC7229040

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.