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dc.date.accessioned2022-10-28T15:45:28Z
dc.date.available2022-10-28T15:45:28Z
dc.date.created2022-09-28T11:26:20Z
dc.date.issued2022
dc.identifier.citationRee, Anne Hansen Mælandsmo, Gunhild Mari Flatmark, Kjersti Russnes, Hege Elisabeth Giercksky Casteneda, Monica Gomez Aas, Eline . Cost-effectiveness of molecularly matched off-label therapies for end-stage cancer–the MetAction precision medicine study. Acta Oncologica. 2022, 61(8), 955-962
dc.identifier.urihttp://hdl.handle.net/10852/97406
dc.description.abstractBackground Precision cancer medicine (PCM), frequently used for the expensive and often modestly efficacious off-label treatment with medications matched to the tumour genome of end-stage cancer, challenges healthcare resources. We compared the health effects, costs and cost-effectiveness of our MetAction PCM study with corresponding data from comparator populations given best supportive care (BSC) in two external randomised controlled trials. Methods We designed three partitioned survival models to evaluate the healthcare costs and quality-adjusted life years (QALYs) as the main outcomes. Cost-effectiveness was calculated as the incremental cost-effectiveness ratio (ICER) of PCM relative to BSC with an annual willingness-to-pay (WTP) threshold of EUR 56,384 (NOK 605,000). One-way and probabilistic sensitivity analyses addressed uncertainty. Results We estimated total healthcare costs (relating to next-generation sequencing (NGS) equipment and personnel wages, molecularly matched medications to the patients with an actionable tumour target and follow-up of the responding patients) and the health outcomes for the MetAction patients versus costs (relating to estimated hospital admission) and outcomes for the BSC cases. The ICERs for incremental QALYs were twice or more as high as the WTP threshold and relatively insensitive to cost decrease of the NGS procedures, while reduction of medication prices would contribute significantly towards a cost-effective PCM strategy. Conclusions The models suggested that the high ICERs of PCM were driven by costs of the NGS diagnostics and molecularly matched medications, with a likelihood for the strategy to be cost-effective defying WTP constraints. Reducing drug expenses to half the list price would likely result in an ICER at the WTP threshold. This can be an incentive for a public-private partnership for sharing drug costs in PCM, exemplified by ongoing European initiatives.
dc.languageEN
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleCost-effectiveness of molecularly matched off-label therapies for end-stage cancer–the MetAction precision medicine study
dc.title.alternativeENEngelskEnglishCost-effectiveness of molecularly matched off-label therapies for end-stage cancer–the MetAction precision medicine study
dc.typeJournal article
dc.creator.authorRee, Anne Hansen
dc.creator.authorMælandsmo, Gunhild Mari
dc.creator.authorFlatmark, Kjersti
dc.creator.authorRussnes, Hege Elisabeth Giercksky
dc.creator.authorCasteneda, Monica Gomez
dc.creator.authorAas, Eline
cristin.unitcode185,53,82,0
cristin.unitnameKlinikk for indremedisin og lab fag
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin2056276
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Acta Oncologica&rft.volume=61&rft.spage=955&rft.date=2022
dc.identifier.jtitleActa Oncologica
dc.identifier.volume61
dc.identifier.issue8
dc.identifier.startpage955
dc.identifier.endpage962
dc.identifier.doihttps://doi.org/10.1080/0284186X.2022.2098053
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn0284-186X
dc.type.versionPublishedVersion
dc.relation.projectNFR/296114


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