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Cladribine: Off-label disease modification for people with multiple sclerosis in resource-poor settings?

BACKGROUND: A considerable number of people with multiple sclerosis (pwMS) live in low- and middle-income countries (LMIC), where lack of resource adversely affects access to effective disease-modifying treatment. OBJECTIVE: The objective of this commentary is to propose a useful cost-effective dise...

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Autores principales: Mao, Zhifeng, Álvarez-Gonzalez, César, De Trane, Stefania, Yildiz, Ozlem, Albor, Christo, Doctor, Gabriel, Soon, Derek, Pepper, George, Turner, Benjamin P, Marta, Monica, Mathews, Joela, Giovannoni, Gavin, Baker, David, Schmierer, Klaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6077935/
https://www.ncbi.nlm.nih.gov/pubmed/30090639
http://dx.doi.org/10.1177/2055217318783767
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author Mao, Zhifeng
Álvarez-Gonzalez, César
De Trane, Stefania
Yildiz, Ozlem
Albor, Christo
Doctor, Gabriel
Soon, Derek
Pepper, George
Turner, Benjamin P
Marta, Monica
Mathews, Joela
Giovannoni, Gavin
Baker, David
Schmierer, Klaus
author_facet Mao, Zhifeng
Álvarez-Gonzalez, César
De Trane, Stefania
Yildiz, Ozlem
Albor, Christo
Doctor, Gabriel
Soon, Derek
Pepper, George
Turner, Benjamin P
Marta, Monica
Mathews, Joela
Giovannoni, Gavin
Baker, David
Schmierer, Klaus
author_sort Mao, Zhifeng
collection PubMed
description BACKGROUND: A considerable number of people with multiple sclerosis (pwMS) live in low- and middle-income countries (LMIC), where lack of resource adversely affects access to effective disease-modifying treatment. OBJECTIVE: The objective of this commentary is to propose a useful cost-effective disease-modifying treatment option for pwMS in LMIC with potential high efficacy and high convenience to the pwMS and treating physician. Viewpoint: We propose using generic 2-chloro-2’-deoxyadenosine (cladribine), a small molecule licensed for treatment of people with hairy cell leukaemia, as a solution of this significant equity imbalance. Cladribine has been shown in phase II and III trials to be a highly effective disease-modifying treatment for pwMS, and its adverse effect profile is comparable with any DMT currently licensed in high-income economies where an oral preparation has recently been licensed by the European Medicines Agency. CONCLUSION: Our viewpoint takes into account experience we have gathered over the past three years in the use of generic cladribine to treat pwMS. Whilst here we focus on MS, there is significant potential for use of cladribine in other conditions that could benefit from its mechanism of action.
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spelling pubmed-60779352018-08-08 Cladribine: Off-label disease modification for people with multiple sclerosis in resource-poor settings? Mao, Zhifeng Álvarez-Gonzalez, César De Trane, Stefania Yildiz, Ozlem Albor, Christo Doctor, Gabriel Soon, Derek Pepper, George Turner, Benjamin P Marta, Monica Mathews, Joela Giovannoni, Gavin Baker, David Schmierer, Klaus Mult Scler J Exp Transl Clin Commentary BACKGROUND: A considerable number of people with multiple sclerosis (pwMS) live in low- and middle-income countries (LMIC), where lack of resource adversely affects access to effective disease-modifying treatment. OBJECTIVE: The objective of this commentary is to propose a useful cost-effective disease-modifying treatment option for pwMS in LMIC with potential high efficacy and high convenience to the pwMS and treating physician. Viewpoint: We propose using generic 2-chloro-2’-deoxyadenosine (cladribine), a small molecule licensed for treatment of people with hairy cell leukaemia, as a solution of this significant equity imbalance. Cladribine has been shown in phase II and III trials to be a highly effective disease-modifying treatment for pwMS, and its adverse effect profile is comparable with any DMT currently licensed in high-income economies where an oral preparation has recently been licensed by the European Medicines Agency. CONCLUSION: Our viewpoint takes into account experience we have gathered over the past three years in the use of generic cladribine to treat pwMS. Whilst here we focus on MS, there is significant potential for use of cladribine in other conditions that could benefit from its mechanism of action. SAGE Publications 2018-06-26 /pmc/articles/PMC6077935/ /pubmed/30090639 http://dx.doi.org/10.1177/2055217318783767 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Commentary
Mao, Zhifeng
Álvarez-Gonzalez, César
De Trane, Stefania
Yildiz, Ozlem
Albor, Christo
Doctor, Gabriel
Soon, Derek
Pepper, George
Turner, Benjamin P
Marta, Monica
Mathews, Joela
Giovannoni, Gavin
Baker, David
Schmierer, Klaus
Cladribine: Off-label disease modification for people with multiple sclerosis in resource-poor settings?
title Cladribine: Off-label disease modification for people with multiple sclerosis in resource-poor settings?
title_full Cladribine: Off-label disease modification for people with multiple sclerosis in resource-poor settings?
title_fullStr Cladribine: Off-label disease modification for people with multiple sclerosis in resource-poor settings?
title_full_unstemmed Cladribine: Off-label disease modification for people with multiple sclerosis in resource-poor settings?
title_short Cladribine: Off-label disease modification for people with multiple sclerosis in resource-poor settings?
title_sort cladribine: off-label disease modification for people with multiple sclerosis in resource-poor settings?
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6077935/
https://www.ncbi.nlm.nih.gov/pubmed/30090639
http://dx.doi.org/10.1177/2055217318783767
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