Evidence map›Paper›PMID 39259243›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2024

Cladribine use trend in Latin America: the changes in patient profile impact in the drug effectiveness.

Berenice A Silva, Alejandra Heriz, Jeremías Ayerbe, Luciana Lázaro, Magdalena Casas, Pablo López, Verónica Tkachuk, María Eugenia Balbuena, Débora Nadur, Susana Liwacki and 20 more

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Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

30 authors.

Berenice A SilvaHospital Italiano de Buenos Aires, Sección Enfermedades Desmielinizantes, Buenos Aires, Argentina. berenice.silva@gmail.com.ORCID http://orcid.org/0000-0001-5866-2419
Alejandra HerizHospital Italiano de Buenos Aires, Sección Enfermedades Desmielinizantes, Buenos Aires, Argentina.
Jeremías AyerbeHospital Italiano de Buenos Aires, Sección Enfermedades Desmielinizantes, Buenos Aires, Argentina.
Luciana LázaroHospital Ramos Mejía, CABA, Hospital Italiano de Buenos Aires and Centro Universitario de Esclerosis Múltiple, Buenos Aires, Argentina.
Magdalena CasasHospital Ramos Mejía, CABA, Hospital Italiano de Buenos Aires and Centro Universitario de Esclerosis Múltiple, Buenos Aires, Argentina.
Pablo LópezHospital Alemán, Unidad de Neuroinmunología, Buenos Aires, Argentina.
Verónica TkachukHospital de Clínicas José de San Martín, Clínica de Enfermedades Desmielinizantes, Buenos Aires, Argentina.
María Eugenia BalbuenaHospital de Clínicas José de San Martín, Clínica de Enfermedades Desmielinizantes, Buenos Aires, Argentina.
Débora NadurHospital de Clínicas José de San Martín, Clínica de Enfermedades Desmielinizantes, Buenos Aires, Argentina.
Susana LiwackiHospital de Córdoba, Servicio de Neurología, Córdoba, Argentina.
Geraldine LueticInstituto de Neurociencias de Rosario, Rosario, Argentina.
Marcos BurgosHospital San Bernardo, Salta, Argentina.
Federico CasalesSanatorio de Los Arcos, Servicio de Neurología, Buenos Aires, Argentina.
Agustina PiedrabuenaSanatorio de Los Arcos, Servicio de Neurología, Buenos Aires, Argentina.
Edgar Carnero ContenttiHospital Alemán, Unidad de Neuroinmunología, Buenos Aires, Argentina.
Agustina ZárateSanatorio Allende, Córdoba, Argentina.
Gisela ZangaUA César Milstein, Buenos Aires, Argentina.
Judith SteinbergHospital Británico, Servicio de Neurología, Buenos Aires, Argentina.
Carolina MainellaHospital Español, Rosario, Argentina.
Darío TavoliniINECO Neurociencias, Rosario, Argentina.
Javier HrybHospital Durand, Consultorio de Neuroinmunología Clínica, Buenos Aires, Argentina.
Felisa LeguizamónHospital Álvarez, Buenos Aires, Argentina.
Fátima Pagani CassaráHospital Austral, Buenos Aires, Argentina.
Gustavo JoséHospital Padilla, Tucumán, Argentina.
Paula CarrizoHospital Padilla, Tucumán, Argentina.
Pedro NofalHospital de Clínicas Nuestra Señora del Carmen, San Miguel de Tucumán, Argentina.
Belén LuisHospital Güemes, Sección Enfermedades Desmielinizantes, Buenos Aires, Argentina.
Cecilia PitaHospital Ramos Mejía, CABA, Hospital Italiano de Buenos Aires and Centro Universitario de Esclerosis Múltiple, Buenos Aires, Argentina.
Jimena MíguezHospital Italiano de Buenos Aires, Sección Enfermedades Desmielinizantes, Buenos Aires, Argentina.
Ricardo AlonsoHospital Ramos Mejía, CABA, Hospital Italiano de Buenos Aires and Centro Universitario de Esclerosis Múltiple, Buenos Aires, Argentina.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCladribine was approved for Multiple Sclerosis (MS) in our country in 2018. A previous study by our group showed that its use among high efficacy therapies options has been increasing along the years.

objectiveto analyze the cladribine use trend across time since its approval.

methodA retrospective cohort study was performed. People with MS (pwMS) treated with cladribine were included. Two periods were defined: P1 = 2018 - 2020 and P2 = 2021 - 2023. A comparative analysis was carry out between P1 and P2 to assess the trend of use, clinical/demographic characteristics, and effectiveness.

resultsOne hundred ninety- seven people with MS (pwMS) were included, mean EDSS: 2.2 ± 3.08, 72.6% female, mean age: 35.2 ± 9 years, mean disease duration: 6.6 ± 5.6 years, mean time lapse under cladribine: 26.1 ± 12.4 months. Regarding patient profile, we found significant differences between P1 and P2 in the MS evolution (p = 0.001) and EDSS ( p = 0.018) prior to initiation of cladribine. In the individualized analysis by year, we found a decrease in relapse number in the year prior to starting cladribine (p = 0.02). A higher proportion of No Evidence of Disease Activity (NEDA) was found in patients treated at P2 compared to those treated at P1 (p < 0.001).

conclusionAn earlier use of cladribine achieved a significant increase in reaching NEDA. This learning curve in the use of cladribine allows a better identification of the candidate patient and influences the treatment effectiveness.

Indexed as

CladribineImmunosuppressive AgentsAdultFemaleHumansLatin AmericaMaleMiddle AgedMultiple SclerosisRetrospective StudiesTreatment OutcomeCladribineImmunosuppressive AgentsCladribineEffectivenessMultiple sclerosisPatient profileTreatmentUse trend

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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.