Evidence map›Paper›PMID 32544164›Full record

SynthesisPloS one2020

Reliability in long-term clinical studies of disease-modifying therapies for relapsing-remitting multiple sclerosis: A systematic review.

Rosa C Lucchetta, Letícia P Leonart, Marcus V M Gonçalves, Jefferson Becker, Roberto Pontarolo, Fernando Fernandez-Llimós, Astrid Wiens

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 33% of its field
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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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

7 authors at 4 institutions in 2 countries.

Rosa C LucchettaGraduate Program in Pharmaceutical Sciences, Federal University of Paraná, Curitiba, Brazil.ORCID 0000-0002-4004-1320
Letícia P LeonartGraduate Program in Pharmaceutical Sciences, Federal University of Paraná, Curitiba, Brazil.
Marcus V M GonçalvesUniversidade da região de Joinville (UNIVILLE), Joinville, Brazil.
Jefferson BeckerBrain Institute and School of Medicine, Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.
Roberto PontaroloGraduate Program in Pharmaceutical Sciences, Federal University of Paraná, Curitiba, Brazil.ORCID 0000-0002-7049-4363
Fernando Fernandez-LlimósLaboratory of Pharmacology, Department of Drug Sciences, Faculty of Pharmacy, University of Porto, Porto, Portugal.
Astrid WiensGraduate Program in Pharmaceutical Sciences, Federal University of Paraná, Curitiba, Brazil.
Universidade Federal do Paraná · BRPontifícia Universidade Católica do Rio Grande do Sul · BRUniversidade da Região de Joinville · BRUniversidade do Porto · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough relapsing-remitting multiple sclerosis (RRMS) has a chronic course, little information is known about the comparison between the disease-modifying therapies (DMT) for long-term outcomes. We aimed to conduct a systematic review of randomized clinical trial (RCT) extension and observational studies to examine the efficacy and safety of all available DMT for RRMS, compare the evidence with that derived from mid-term studies, and investigate whether the published long-term data are robust and reliable enough to inform clinical decision-making concerning RRMS treatment.

methodPubMed, Scopus, and manual searches were performed until October 2019. The clinical outcomes of long- and mid-term studies were compared. ROBINS-I was used to assess the methodological qualities of the long-term studies. PROSPERO number CRD42019123361.

resultsNineteen long-term studies (9,018 participants) were included in the systematic review. All studies presented serious or critical risks of bias that were mainly due to confounding, selection, and missing data biases. The annualised relapse rates (ARR) observed in the long-term studies are lower (better) than those from the mid-term studies for most treatments. The main reason for this ARR decrease could be a selection bias for good responders in the long-term studies, since many studies show a loss of patients between the mid- and long-term phases. The safety profiles depend on the study, follow-up, report, and outcome (i.e., discontinuation or number of patients with at least one serious adverse event).

conclusionThe currently available long-term data for patients with RRMS exhibit serious or critical risks of bias that preclude robust comparisons between long-term studies. High quality comparative observational studies with long-term follow-ups or RCT extensions with intention-to-treat analyses are needed to support clinical and regulatory practice. Until reliable long-term evidence is available, neurologists should continue to base their conduct on mid-term studies, patient`s experience and, most importantly, patient`s needs and predictor factors, according to personalized medicine.

Indexed as

Databases, FactualHumansMultiple Sclerosis, Relapsing-RemittingRandomized Controlled Trials as TopicRecurrenceTime FactorsTreatment Outcome

Identifiers

PMID32544164
PMCPMC7297314
OpenAlexW3034588488

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.