Evaluation of Study and Patient Characteristics of Clinical Studies in Primary Progressive Multiple Sclerosis: A Systematic Review.

<h4>Background</h4>So far, clinical studies in primary progressive MS (PPMS) have failed to meet their primary efficacy endpoints. To some extent this might be attributable to the choice of assessments or to the selection of the study population.<h4>Objective</h4>The aim of t...

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Main Authors: T Ziemssen, S Rauer, C Stadelmann, T Henze, J Koehler, I-K Penner, M Lang, D Poehlau, M Baier-Ebert, H Schieb, S Meuth
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0138243
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author T Ziemssen
S Rauer
C Stadelmann
T Henze
J Koehler
I-K Penner
M Lang
D Poehlau
M Baier-Ebert
H Schieb
S Meuth
author_facet T Ziemssen
S Rauer
C Stadelmann
T Henze
J Koehler
I-K Penner
M Lang
D Poehlau
M Baier-Ebert
H Schieb
S Meuth
author_sort T Ziemssen
collection DOAJ
description <h4>Background</h4>So far, clinical studies in primary progressive MS (PPMS) have failed to meet their primary efficacy endpoints. To some extent this might be attributable to the choice of assessments or to the selection of the study population.<h4>Objective</h4>The aim of this study was to identify outcome influencing factors by analyzing the design and methods of previous randomized studies in PPMS patients without restriction to intervention or comparator.<h4>Methods</h4>A systematic literature search was conducted in MEDLINE, EMBASE, BIOSIS and the COCHRANE Central Register of Controlled Trials (inception to February 2015). Keywords included PPMS, primary progressive multiple sclerosis and chronic progressive multiple sclerosis. Randomized, controlled trials of at least one year's duration were selected if they included only patients with PPMS or if they reported sufficient PPMS subgroup data. No restrictions with respect to intervention or comparator were applied. Study quality was assessed by a biometrics expert. Relevant baseline characteristics and outcomes were extracted and compared.<h4>Results</h4>Of 52 PPMS studies identified, four were selected. Inclusion criteria were notably different among studies with respect to both the definition of PPMS and the requirements for the presence of disability progression at enrolment. Differences between the study populations included the baseline lesion load, pretreatment status and disease duration. The rate of disease progression may also be an important factor, as all but one of the studies included a large proportion of patients with a low progression rate. In addition, the endpoints specified could not detect progression adequately.<h4>Conclusion</h4>Optimal PPMS study methods involve appropriate patient selection, especially regarding the PPMS phenotype and progression rate. Functional composite endpoints might be more sensitive than single endpoints in capturing progression.
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spelling doaj-art-308eba5138fa4a8b83ff21f5bfdfdaec2025-08-20T03:49:56ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01109e013824310.1371/journal.pone.0138243Evaluation of Study and Patient Characteristics of Clinical Studies in Primary Progressive Multiple Sclerosis: A Systematic Review.T ZiemssenS RauerC StadelmannT HenzeJ KoehlerI-K PennerM LangD PoehlauM Baier-EbertH SchiebS Meuth<h4>Background</h4>So far, clinical studies in primary progressive MS (PPMS) have failed to meet their primary efficacy endpoints. To some extent this might be attributable to the choice of assessments or to the selection of the study population.<h4>Objective</h4>The aim of this study was to identify outcome influencing factors by analyzing the design and methods of previous randomized studies in PPMS patients without restriction to intervention or comparator.<h4>Methods</h4>A systematic literature search was conducted in MEDLINE, EMBASE, BIOSIS and the COCHRANE Central Register of Controlled Trials (inception to February 2015). Keywords included PPMS, primary progressive multiple sclerosis and chronic progressive multiple sclerosis. Randomized, controlled trials of at least one year's duration were selected if they included only patients with PPMS or if they reported sufficient PPMS subgroup data. No restrictions with respect to intervention or comparator were applied. Study quality was assessed by a biometrics expert. Relevant baseline characteristics and outcomes were extracted and compared.<h4>Results</h4>Of 52 PPMS studies identified, four were selected. Inclusion criteria were notably different among studies with respect to both the definition of PPMS and the requirements for the presence of disability progression at enrolment. Differences between the study populations included the baseline lesion load, pretreatment status and disease duration. The rate of disease progression may also be an important factor, as all but one of the studies included a large proportion of patients with a low progression rate. In addition, the endpoints specified could not detect progression adequately.<h4>Conclusion</h4>Optimal PPMS study methods involve appropriate patient selection, especially regarding the PPMS phenotype and progression rate. Functional composite endpoints might be more sensitive than single endpoints in capturing progression.https://doi.org/10.1371/journal.pone.0138243
spellingShingle T Ziemssen
S Rauer
C Stadelmann
T Henze
J Koehler
I-K Penner
M Lang
D Poehlau
M Baier-Ebert
H Schieb
S Meuth
Evaluation of Study and Patient Characteristics of Clinical Studies in Primary Progressive Multiple Sclerosis: A Systematic Review.
PLoS ONE
title Evaluation of Study and Patient Characteristics of Clinical Studies in Primary Progressive Multiple Sclerosis: A Systematic Review.
title_full Evaluation of Study and Patient Characteristics of Clinical Studies in Primary Progressive Multiple Sclerosis: A Systematic Review.
title_fullStr Evaluation of Study and Patient Characteristics of Clinical Studies in Primary Progressive Multiple Sclerosis: A Systematic Review.
title_full_unstemmed Evaluation of Study and Patient Characteristics of Clinical Studies in Primary Progressive Multiple Sclerosis: A Systematic Review.
title_short Evaluation of Study and Patient Characteristics of Clinical Studies in Primary Progressive Multiple Sclerosis: A Systematic Review.
title_sort evaluation of study and patient characteristics of clinical studies in primary progressive multiple sclerosis a systematic review
url https://doi.org/10.1371/journal.pone.0138243
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