ECTRIMS eLearning

Estimating the long-term effect of drugs in multiple sclerosis
Author(s): ,
C Cordioli
Affiliations:
Multiple Sclerosis Centre, Spedali Civili, Montichiari
,
S Rasia
Affiliations:
Multiple Sclerosis Centre, Spedali Civili, Montichiari
,
F Gallo
Affiliations:
Section of Biostatistics, Department of Health Sciences (DISSAL), University of Genoa, Genova, Italy
,
R Capra
Affiliations:
Multiple Sclerosis Centre, Spedali Civili, Montichiari
M.P Sormani
Affiliations:
Section of Biostatistics, Department of Health Sciences (DISSAL), University of Genoa, Genova, Italy
ECTRIMS Learn. Cordioli C. 09/15/16; 146140; P299
Cinzia Cordioli
Cinzia Cordioli
Contributions
Abstract

Abstract: P299

Type: Poster

Abstract Category: Clinical aspects of MS - Natural course

Background: In multiple sclerosis (MS) there is no certainty to what extent the short-term effects of drugs translate into long-term benefits for patients. Observational studies devoted to clarify this issue are affected by selection bias: treated and untreated patients are different and their difference is likely related to prognosis.

Goals
: To evaluate whether the introduction of therapies changed the MS prognosis, assessing the age at which patients diagnosed in different periods (pre and post therapies approval) reached EDSS milestones, with no comparisons of treated and untreated patients.

Methods: We retrospectively analysed a large dataset of MS outpatients evaluated at the MS Centre of Montichiari (Brescia, Italy) between 1985 and 2013, with an initial RRMS course and age at diagnosis 18-60 years. Age at which patients reached EDSS 6 was compared according to year of diagnosis (grouping patients diagnosed in 1980-1990, 1991-1995, 1996-2000, 2001-2005, 2006-2010, 2011+), by a Cox model adjusted for mean age at diagnosis and EDSS visits frequency.

Results: 1324 RRMS patients were included. The average age at onset was 32.4 years (SD= 9.6, range =13-59 years) and the average age at diagnosis was 35.6 years (SD= 10.0, 18-60 years). The age at diagnosis increased from 32 to 37 years (p< 0.001) in more recent years. Patients diagnosed in more recent periods reached EDSS=6 at higher age: taking patients diagnosed before 1990 as a reference, the probability to reach EDSS=6 was similar in patients diagnosed in the period 1991-1995 (HR=1.09), it was reduced by 15% in patients diagnosed in 1996-2000 (HR=0.85, p=0.44), by 37% in patients diagnosed in 2001-2005 (HR=0.63, p=0.05), by 46% in patients diagnosed in 2006-2010 (HR=0.54, p< 0.02). The proportion of patients diagnosed before 2000 who reached EDSS=6 at the age of 50 years was 27% and 15% after 2000 (p< 0.001).

Conclusions: A clear modification of MS course is observed after 2000, with 4 years delay since 1996 (introduction of first DMTs in Italy), when the proportion of patients steadily treated was increasing. A second leap coincides with the introduction of second-line treatments (natalizumab, fingolimod).

Disclosure:

Cinzia Cordioli: consulting fees from Merk-Serono;

Sarah Rasia: nothing to disclose;

Ruggero Capra: received consulting fees from Novartis, Biogen and lecture fees and/or travel grants from Novartis, BiogenIdec, Genzyme and Sanofi-Aventis.

Maria Pia Sormani: received personal compensation for consulting services and for speaking activities from Novartis, Roche, Genzyme, Merck Serono, Teva, Synthon and Biogen Idec;

Fabio Gallo: nothing to disclose.

Abstract: P299

Type: Poster

Abstract Category: Clinical aspects of MS - Natural course

Background: In multiple sclerosis (MS) there is no certainty to what extent the short-term effects of drugs translate into long-term benefits for patients. Observational studies devoted to clarify this issue are affected by selection bias: treated and untreated patients are different and their difference is likely related to prognosis.

Goals
: To evaluate whether the introduction of therapies changed the MS prognosis, assessing the age at which patients diagnosed in different periods (pre and post therapies approval) reached EDSS milestones, with no comparisons of treated and untreated patients.

Methods: We retrospectively analysed a large dataset of MS outpatients evaluated at the MS Centre of Montichiari (Brescia, Italy) between 1985 and 2013, with an initial RRMS course and age at diagnosis 18-60 years. Age at which patients reached EDSS 6 was compared according to year of diagnosis (grouping patients diagnosed in 1980-1990, 1991-1995, 1996-2000, 2001-2005, 2006-2010, 2011+), by a Cox model adjusted for mean age at diagnosis and EDSS visits frequency.

Results: 1324 RRMS patients were included. The average age at onset was 32.4 years (SD= 9.6, range =13-59 years) and the average age at diagnosis was 35.6 years (SD= 10.0, 18-60 years). The age at diagnosis increased from 32 to 37 years (p< 0.001) in more recent years. Patients diagnosed in more recent periods reached EDSS=6 at higher age: taking patients diagnosed before 1990 as a reference, the probability to reach EDSS=6 was similar in patients diagnosed in the period 1991-1995 (HR=1.09), it was reduced by 15% in patients diagnosed in 1996-2000 (HR=0.85, p=0.44), by 37% in patients diagnosed in 2001-2005 (HR=0.63, p=0.05), by 46% in patients diagnosed in 2006-2010 (HR=0.54, p< 0.02). The proportion of patients diagnosed before 2000 who reached EDSS=6 at the age of 50 years was 27% and 15% after 2000 (p< 0.001).

Conclusions: A clear modification of MS course is observed after 2000, with 4 years delay since 1996 (introduction of first DMTs in Italy), when the proportion of patients steadily treated was increasing. A second leap coincides with the introduction of second-line treatments (natalizumab, fingolimod).

Disclosure:

Cinzia Cordioli: consulting fees from Merk-Serono;

Sarah Rasia: nothing to disclose;

Ruggero Capra: received consulting fees from Novartis, Biogen and lecture fees and/or travel grants from Novartis, BiogenIdec, Genzyme and Sanofi-Aventis.

Maria Pia Sormani: received personal compensation for consulting services and for speaking activities from Novartis, Roche, Genzyme, Merck Serono, Teva, Synthon and Biogen Idec;

Fabio Gallo: nothing to disclose.

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