Evidence map›Paper›PMID 42828703›Full record

ArticleNeurology and therapy2026

Horizon Scanning of Multiple Sclerosis Expenditure in Italy (2025-2029): Updated Insights from the Oracle Model.

Diego Centonze, Massimiliano Calabrese, Eleonora Cocco, Roberta Di Turi, Andrea Marcellusi, Andrea Marinozzi, Maria Vittoria Azzi, Alessandro Carrera, Francesca Donnaloja, Francesco Patti and 1 more

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Article in Neurology and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

11 authors.

Diego CentonzeDepartment of Systems Medicine, Tor Vergata University, Rome, Italy.
Massimiliano CalabreseDepartment of Neuroscience, Biomedicine and Movements, University of Verona, Verona, Italy.
Eleonora CoccoDipartimento Di Scienze Mediche E Sanità Pubblica, Centro Regionale Sclerosi Multipla, ASSL Cagliari, ATS Sardegna, Università Di Cagliari, Cagliari, Italy.
Roberta Di TuriDipartimento Dei Servizi, Hospital Pharmacy, ASL Roma 3, Rome, Italy.
Andrea MarcellusiDepartment of Pharmaceutical Science (DISFARM), University of Milan, Milan, Italy.
Andrea MarinozziUnità Operativa Complessa Di Farmacia Ospedaliera, Ospedale Giuseppe Mazzini, Teramo, Italy.
Maria Vittoria AzziSanofi S.r.l., Milan, Italy.
Alessandro CarreraIQVIA Solutions Italy S.r.l., Milan, Italy.
Francesca DonnalojaIQVIA Solutions Italy S.r.l., Milan, Italy. francesca.donnaloja@iqvia.com.ORCID http://orcid.org/0000-0001-9927-309X
Francesco PattiDepartment of Medical and Surgical Sciences and Advanced Technologies, GF Ingrassia, University of Catania, IQVIA Solutions Italy S.r.l., Via Fabio Filzi 29, 20124, Catania, MI, Italy.
Oracle 3.0 study group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMultiple sclerosis (MS) is a chronic and progressively disabling neurological disease associated with a substantial clinical and socioeconomic burden. The introduction of an increasing number of new innovative therapies has further intensified concerns regarding the long-term sustainability for the Italian National Healthcare Service (NHS). Despite substantial therapeutic progress in MS management, with several treatments available for most MS patient populations, no definitive cure is currently available, and a critical therapeutic gap persists for non-relapsing secondary progressive MS (NR-SPMS), for which no approved treatments are specifically indicated. The objective of the present research is to estimate the Italian NHS expenditure for MS disease-modifying therapies (DMTs) between 2025 and 2029.

methodsBuilding on a published horizon-scanning model (i.e., Oracle), this study updates projections of expenditure and treatment patterns for MS DMTs through 2029, integrating clinical inputs (i.e., treated patients, patient shares for each reimbursed therapy) with economic inputs (i.e., annual therapy costs). Assumptions and input data were derived from IQVIA® proprietary databases and informed by clinical and pharmacoeconomic expert inputs. Results were validated in a multi-stakeholder roundtable.

resultsThis study shows that the number of treated patients is projected to rise to about 77,000 by 2029, i.e., approximately + 10% from 2024. Traditional platform therapies are projected to decrease by more than ten percentage points between 2024 and 2029, reflecting a shift toward high-efficacy and innovative therapies. New options include Bruton's tyrosine kinase (BTK) inhibitors (e.g., tolebrutinib, fenebrutinib, remibrutinib), projected to reach approximately 16% patient share within 3 years of first launch.

conclusionDespite higher patient volumes and new launches, total DMT expenditure is expected to decline from €784 million in 2024 to €622 million in 2029, mainly driven by losses of exclusivity and price renegotiations. Results support the sustainability of the NHS and the reallocation of resources toward innovation, including innovative therapies for currently underserved populations such as NR-SPMS.

Indexed as

BTKiDMTsForecastHorizon scanning modelItalian National Healthcare Service expenditureMultiple sclerosisNR-SPMS

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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.