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Conference Paper: Cost-effectiveness analysis of additional abiraterone for hormone-sensitive metastatic prostatic cancer treated with androgen deprivation therapy (ADT)

TitleCost-effectiveness analysis of additional abiraterone for hormone-sensitive metastatic prostatic cancer treated with androgen deprivation therapy (ADT)
Authors
Issue Date2017
PublisherOxford University Press. The Journal's web site is located at http://annonc.oxfordjournals.org/
Citation
European Society for Medical Oncology (ESMO) Asia Congress, Singapore, 17–19 November 2017. In Annals of Oncology, 2017, v. 28 n. Suppl. 10, p. x77, abstract no. 261O How to Cite?
AbstractBackground: The recent LATITUDE trial showed that Abiraterone plus Prednisolone (AP) combined with androgen deprivation therapy (ADT) significantly improved overall survival of patients with hormone-sensitive metastatic prostatic cancer. We conducted a study aims to evaluate whether AP plus ADT is a cost-effective strategy from Hong Kong perspective. Methods: The current cost-effectiveness analysis (CEA) considered the reported efficacy of AP in the large-scale randomized clinical trial (LATITUDE) that recruited 1,917 patients of advanced prostate cancer, among which 1,002 had metastatic disease. Using a deterministic Markov model with probabilistic sensitivity analysis (PSA) for accounting parameter uncertainty, AP plus ADT was compared with ADT-alone in patients with metastases across a 20-year time horizon. Quality-adjusted life-year (QALY) and incremental cost-effectiveness ratio (ICER) were applied as the primary outcomes. The study took Hong Kong’s societal perspective and the WHO’s recommendation of 3 times the local gross domestic product (GDP) per capita (USD$43,530/HKD$339,531 in 2016) was used as the threshold of cost-effectiveness. Results: The ICER of adding AP on top of ADT was USD$183,003 (median, 95% central range [CR] USD$148,780-235,632; approximately HKD$1,427,425, CR HKD$1,160,480-1,837,926) per QALY gained. Referring to the WHO’s recommended cost-effective threshold, AP plus ADT was not a cost-effective strategy compared with the current ADT-alone standard care strategy. The combined strategy of AP plus ADT, however, would be cost-effective if the cost of AP were reduced to USD$3,116 (median, approximately HKD$24,304) per cycle, which is around 72% of its current price in Hong Kong public hospital. Conclusions: Despite the survival benefit and that Hong Kong is well-developed with high global ranking in GDP per capita, adding AP to ADT is not recommended as a cost-effective treatment in metastatic hormone sensitive prostatic cancer in Hong Kong setting.
Persistent Identifierhttp://hdl.handle.net/10722/256464
ISSN
2023 Impact Factor: 56.7
2023 SCImago Journal Rankings: 13.942
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChiang, CL-
dc.contributor.authorChoi, CW-
dc.contributor.authorMui, WH-
dc.contributor.authorSo, TH-
dc.date.accessioned2018-07-20T06:35:05Z-
dc.date.available2018-07-20T06:35:05Z-
dc.date.issued2017-
dc.identifier.citationEuropean Society for Medical Oncology (ESMO) Asia Congress, Singapore, 17–19 November 2017. In Annals of Oncology, 2017, v. 28 n. Suppl. 10, p. x77, abstract no. 261O-
dc.identifier.issn0923-7534-
dc.identifier.urihttp://hdl.handle.net/10722/256464-
dc.description.abstractBackground: The recent LATITUDE trial showed that Abiraterone plus Prednisolone (AP) combined with androgen deprivation therapy (ADT) significantly improved overall survival of patients with hormone-sensitive metastatic prostatic cancer. We conducted a study aims to evaluate whether AP plus ADT is a cost-effective strategy from Hong Kong perspective. Methods: The current cost-effectiveness analysis (CEA) considered the reported efficacy of AP in the large-scale randomized clinical trial (LATITUDE) that recruited 1,917 patients of advanced prostate cancer, among which 1,002 had metastatic disease. Using a deterministic Markov model with probabilistic sensitivity analysis (PSA) for accounting parameter uncertainty, AP plus ADT was compared with ADT-alone in patients with metastases across a 20-year time horizon. Quality-adjusted life-year (QALY) and incremental cost-effectiveness ratio (ICER) were applied as the primary outcomes. The study took Hong Kong’s societal perspective and the WHO’s recommendation of 3 times the local gross domestic product (GDP) per capita (USD$43,530/HKD$339,531 in 2016) was used as the threshold of cost-effectiveness. Results: The ICER of adding AP on top of ADT was USD$183,003 (median, 95% central range [CR] USD$148,780-235,632; approximately HKD$1,427,425, CR HKD$1,160,480-1,837,926) per QALY gained. Referring to the WHO’s recommended cost-effective threshold, AP plus ADT was not a cost-effective strategy compared with the current ADT-alone standard care strategy. The combined strategy of AP plus ADT, however, would be cost-effective if the cost of AP were reduced to USD$3,116 (median, approximately HKD$24,304) per cycle, which is around 72% of its current price in Hong Kong public hospital. Conclusions: Despite the survival benefit and that Hong Kong is well-developed with high global ranking in GDP per capita, adding AP to ADT is not recommended as a cost-effective treatment in metastatic hormone sensitive prostatic cancer in Hong Kong setting.-
dc.languageeng-
dc.publisherOxford University Press. The Journal's web site is located at http://annonc.oxfordjournals.org/-
dc.relation.ispartofEuropean Society for Medical Oncology (ESMO) Asia Congress, 2017-
dc.relation.ispartofAnnals of Oncology-
dc.titleCost-effectiveness analysis of additional abiraterone for hormone-sensitive metastatic prostatic cancer treated with androgen deprivation therapy (ADT)-
dc.typeConference_Paper-
dc.identifier.emailChiang, CL: chiangcl@hku.hk-
dc.identifier.emailChoi, CW: hcchoi@hku.hk-
dc.identifier.emailSo, TH: sth495@hku.hk-
dc.identifier.authorityChiang, CL=rp02241-
dc.identifier.authoritySo, TH=rp01981-
dc.description.natureabstract-
dc.identifier.doi10.1093/annonc/mdx662-
dc.identifier.hkuros286201-
dc.identifier.hkuros303696-
dc.identifier.volume28-
dc.identifier.issueSuppl. 10-
dc.identifier.spagex77, abstract no. 261O-
dc.identifier.epagex77, abstract no. 261O-
dc.identifier.isiWOS:000425626900270-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl0923-7534-

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