Evidence map›Paper›PMID 42665347›Full record

ArticleBMJ open2026

Health-system burden of higher-risk myelodysplastic syndromes in England: a literature-based micro-cost analysis.

Joab Williamson, Emma J Searle, Elina Louramo, Ralph Hughes, Petri Bono, Vijay S Gc

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Article in BMJ open, 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

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Joab WilliamsonFaron Pharmaceuticals Oy, Turku, Southwest Finland, Finland joab.williamson@faron.com.ORCID 0000-0002-8306-1559
Emma J SearleThe Christie NHS Foundation Trust, Manchester, UK.
Elina LouramoFaron Pharmaceuticals Oy, Turku, Southwest Finland, Finland.
Ralph HughesFaron Pharmaceuticals Oy, Turku, Southwest Finland, Finland.
Petri BonoFaron Pharmaceuticals Oy, Turku, Southwest Finland, Finland.ORCID 0000-0003-3963-0416
Vijay S GcCentre for Health Economics, University of York, York, UK.ORCID 0000-0003-0365-2605

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo quantify the per-patient-per-month (PPPM) cost for each phase of care in higher-risk myelodysplastic syndromes (HR-MDS) and the overall cost of a base-case (illustrative) non-curative management pathway followed by a patient with HR-MDS in England.

designWe conducted a retrospective, literature-based, micro-costing analysis from the National Health Service (NHS) England provider perspective using published sources and publicly available price lists. No individual-patient data were used. Based on literature, a base-case management pathway followed by a patient with HR-MDS was defined as a diagnostic work-up at month 0, 12 cycles of azacitidine (given for 7 days in each 28-day cycle), 5 months of post-hypomethylating agent (HMA) failure supportive care and 1 month of terminal care.

settingHealthcare resource utilisation was analysed for adults with HR-MDS who received first-line azacitidine in routine practice if cycle-level or phase-level transfusion and admission rates were reported in the literature. Patients who required allogeneic haematopoietic stem cell transplantation or whose HR-MDS transformed to acute myeloid leukaemia were excluded because the diagnostic and/or therapeutic pathways differ. Unit costs for 2024/2025 were taken from published English national sources and an English trust tariff.

resultsPPPM costs were £8721.58 during active azacitidine therapy, £5399.58 after HMA failure and £12 554.58 for hospital-dominant terminal care; a one-off diagnostic work-up with genomics cost £2710 to £2810. The total cost for the base-case management pathway was £146 921 per patient. An alternative pathway excluding genomic testing and assuming hospice-dominant terminal care reduced the total cost to approximately £136 840 to £140 990, depending on whether the lower or upper bound of hospice bed-day costs is applied.

conclusionsThe direct NHS-provider cost burden of this non-curative HR-MDS management pathway is concentrated in azacitidine acquisition and administration during active treatment, transfusions and admissions after HMA failure and setting-dependent costs at the end of life. The total cost for the illustrative management pathway followed by a patient with HR-MDS (£146 921) is of a similar order to the estimate in the National Institute for Health and Care Excellence technology appraisal for azacitidine uprated to £124 848 for 2024/2025. This comparison is provided for context only and should not be interpreted as validation of the present model, given differences in population, model structure, treatment duration and price year. The phase-specific PPPM estimates can inform, subject to local validation and scenario testing, UK budget-impact analyses, service planning and future economic models.

Indexed as

Health Care CostsMyelodysplastic SyndromesAntimetabolites, AntineoplasticAzacitidineCost-Benefit AnalysisCosts and Cost AnalysisEnglandHumansRetrospective StudiesState MedicineAntimetabolites, AntineoplasticAzacitidineHealth economicsLeukaemiaPrimary CarePublic Hospitals

Identifiers

PMID42665347
PMCPMC13536089

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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.