Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/23641
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dc.contributor.authorGlover, M-
dc.contributor.authorCaplin, M-
dc.contributor.authorLeeuwenkamp, OR-
dc.contributor.authorLongworth, L-
dc.date.accessioned2021-11-30T10:26:31Z-
dc.date.available2021-11-30T10:26:31Z-
dc.date.issued2021-11-09-
dc.identifier.citationGlover, M., Caplin, M., Leeuwenkamp, O.R. and Longworth, L. (2021) 'Use of [<sup>177</sup>Lu]Lu-DOTA-TATE in the treatment of gastroenteropancreatic neuroendocrine tumours: Results of a UK cost-effectiveness modelling study', European Journal of Cancer, Supplement, 16, pp. 14 - 23. doi: 10.1016/j.ejcsup.2021.06.003.en_US
dc.identifier.issn1359-6349-
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/23641-
dc.description.abstractCopyright © 2021 The Author(s). Aim: To evaluate the cost-effectiveness of [177Lu]Lu-DOTA-TATE versus relevant comparators for the treatment of neuroendocrine tumours located in the gastrointestinal tract (GI-NETs) and the pancreas (P-NETs). Materials and methods: A three-state partitioned survival model was developed to perform a cost-utility analysis of [177Lu]Lu-DOTA-TATE versus standard of care (high dose Octreotide LAR), everolimus and sunitinib. Effectiveness data for SoC, everolimus and sunitinib were obtained from published Kaplan–Meier survival curves. Given a lack of head-to-head effectiveness data, matching adjusted indirect comparisons (MAICs) were performed to population-adjust [177Lu]Lu-DOTA-TATE survival data based on prognostic factors and derive estimates of relative effectiveness. Health state utilities were estimated from real-world evidence. Drug acquisition costs were taken from nationally published sources (BNF, NICE), and administration costs were based on treatment protocols in [177Lu]Lu-DOTA-TATE studies, combined with nationally published unit costs (PSSRU, DoH reference costs). Incidence of adverse events were estimated using published sources. A discount rate of 3.5% was applied to both utilities and costs, and deterministic and probabilistic sensitivity analyses were performed. Costs were included from an NHS perspective and presented in 2017/18 GBP (and PPP Euros for base case). Results: In GI-NETs, the incremental cost-effectiveness ratio (ICER) of [177Lu]Lu-DOTA-TATE compared to SoC and everolimus was £26,528 (€27,672) and £24,145 (€25,186) per QALY, respectively. In P-NETs, the ICER of [177Lu]Lu-DOTA-TATE compared to SoC was £22,146 (€23,101) or £28,038 (€29,251) dependent on matched population, and £21,827 (€22,766) and £15,768 (€16,445) compared to everolimus and sunitinib, respectively. Conclusions: At a willingness to pay threshold of £30,000, [177Lu]Lu-DOTA-TATE is likely to be a cost-effective treatment option for GI-NET and P-NET patients versus relevant treatment comparators (NHS perspective).en_US
dc.description.sponsorshipAdvanced Accelerator Applications (AAA), a Novartis company.en_US
dc.format.extent14 - 23-
dc.format.mediumPrint-Electronic-
dc.language.isoen_USen_US
dc.rights© 2021 Published by Elsevier Ltd. This is an open access article under the CC BY-NC-NDlicense (https://creativecommons.org/licenses/by-nc-nd/4.0/)-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.subjectGastro-enteropancreatic neuroendocrine tumours (GEP-NETs)177en_US
dc.subject177-Lu-DOTA-octreotateen_US
dc.subject[177Lu]Lu-DOTA-TATEen_US
dc.subjectEverolimusen_US
dc.subjectSunitiniben_US
dc.subjectQuality-Adjusted Life Years (QALYs)en_US
dc.titleUse of [<sup>177</sup>Lu]Lu-DOTA-TATE in the treatment of gastroenteropancreatic neuroendocrine tumours: Results of a UK cost-effectiveness modelling studyen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.1016/j.ejcsup.2021.06.003-
dc.relation.isPartOfEuropean Journal of Cancer, Supplement-
pubs.publication-statusPublished-
pubs.volume16-
dc.identifier.eissn1878-1217-
Appears in Collections:Dept of Health Sciences Research Papers

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