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dc.contributor.authorCrathorne, Louise
dc.contributor.authorHuxley, N
dc.contributor.authorHaasova, Marcela
dc.contributor.authorSnowsill, T
dc.contributor.authorJones-Hughes, T
dc.contributor.authorHoyle, M
dc.contributor.authorBriscoe, Simon
dc.contributor.authorCoelho, H
dc.contributor.authorLong, Linda
dc.contributor.authorMedina-Lara, A
dc.contributor.authorMujica-Mota, Ruben
dc.contributor.authorNapier, Mark
dc.contributor.authorHyde, C
dc.date.accessioned2016-02-19T09:43:24Z
dc.date.issued2016-02
dc.description.abstractBackground: Anaemia is a common side-effect of cancer treatments and can lead to a reduction in quality of life. Erythropoiesis-stimulating agents (ESAs) are licensed for use in conjunction with red blood cell transfusions (RBCTs) to improve cancer treatment-induced anaemia (CIA). Methods: The clinical effectiveness review followed principles published by NHS CRD. Randomised controlled trials (RCTs), or systematic reviews of RCTs, of ESAs (epoetin or darbepoetin) for treating people with CIA were eligible for inclusion in the review. Comparators were best supportive care (BSC), placebo, or other ESA. Anaemia- and malignancy-related outcomes, health-related quality of life (HRQoL), and adverse events (AEs) were evaluated. Where appropriate, data were pooled using meta-analysis. An empirical health economic model was developed comparing ESA treatment to no ESA treatment. The model has two components: one evaluating short-term costs and QALYs (while patients are anaemic); and one evaluating long-term QALYs. Costs and benefits were discounted at 3.5% pa. Probabilistic and univariate deterministic sensitivity analyses were performed. Results: Twenty-three studies assessing ESAs within their licensed indication (based on start dose administered) were included. None of the RCTs were completely aligned with current EU licenses. Results suggest that there is clinical benefit from ESAs for anaemia-related outcomes. Data suggest improvement in HRQoL scores. The impact of ESAs on AEs and survival remains highly uncertain; although point estimates are lower confidence intervals are wide and not statistically significant. Base case incremental cost-effectiveness ratios (ICERs) for ESA treatment versus no ESA treatment ranged from £19,429–£35,018 per quality-adjusted life year (QALY) gained, but sensitivity and scenario analyses demonstrate considerable uncertainty in these ICERs, including the possibility of overall health disbenefit. All ICERs were sensitive to survival and cost. Conclusions: ESAs could be cost-effective when used closer to licence but there is considerable uncertainty mainly due to unknown impacts on overall survival.en_GB
dc.identifier.citationHTA - 12/42/01en_GB
dc.identifier.urihttp://hdl.handle.net/10871/19955
dc.language.isoenen_GB
dc.publisherNIHR Health Technology Assessment Programmeen_GB
dc.relation.urlhttp://www.nets.nihr.ac.uk/projects/hta/124201en_GB
dc.subjecthealth technology assessmenten_GB
dc.subjectsystematic reviewen_GB
dc.subjecterythropoiesis-stimulating agentsen_GB
dc.subjectcancer-treatment induced anaemiaen_GB
dc.subjectcost effectivenessen_GB
dc.subjectquality-adjusted life yearsen_GB
dc.subjectUKen_GB
dc.subjectNational Institute for Health and Care Excellenceen_GB
dc.subjectclinical effectivenessen_GB
dc.subjectepoetin alfaen_GB
dc.subjectepoetin betaen_GB
dc.subjectepoetin thetaen_GB
dc.subjectepoetin zetaen_GB
dc.subjectepoetinen_GB
dc.subjecterythropoetinen_GB
dc.titleThe effectiveness and cost-effectiveness of erythropoiesis-stimulating agents (epoetin and darbepoetin) for treating cancer-treatment induced anaemia (including review of TA142): a systematic review and economic modelen_GB
dc.typeReporten_GB
dc.date.available2016-02-19T09:43:24Z
dc.identifier.issn1366-5278
exeter.place-of-publicationUnited Kingdom
dc.identifier.journalHealth Technology Assessmenten_GB


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