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Conference Paper: Cost-effectiveness analysis of additional abiraterone for hormone-sensitive metastatic prostatic cancer treated with androgen deprivation therapy (ADT)
Title | Cost-effectiveness analysis of additional abiraterone for hormone-sensitive metastatic prostatic cancer treated with androgen deprivation therapy (ADT) |
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Authors | |
Issue Date | 2017 |
Publisher | Oxford 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? |
Abstract | Background: 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 Identifier | http://hdl.handle.net/10722/256464 |
ISSN | 2023 Impact Factor: 56.7 2023 SCImago Journal Rankings: 13.942 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Chiang, CL | - |
dc.contributor.author | Choi, CW | - |
dc.contributor.author | Mui, WH | - |
dc.contributor.author | So, TH | - |
dc.date.accessioned | 2018-07-20T06:35:05Z | - |
dc.date.available | 2018-07-20T06:35:05Z | - |
dc.date.issued | 2017 | - |
dc.identifier.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 | - |
dc.identifier.issn | 0923-7534 | - |
dc.identifier.uri | http://hdl.handle.net/10722/256464 | - |
dc.description.abstract | Background: 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.language | eng | - |
dc.publisher | Oxford University Press. The Journal's web site is located at http://annonc.oxfordjournals.org/ | - |
dc.relation.ispartof | European Society for Medical Oncology (ESMO) Asia Congress, 2017 | - |
dc.relation.ispartof | Annals of Oncology | - |
dc.title | Cost-effectiveness analysis of additional abiraterone for hormone-sensitive metastatic prostatic cancer treated with androgen deprivation therapy (ADT) | - |
dc.type | Conference_Paper | - |
dc.identifier.email | Chiang, CL: chiangcl@hku.hk | - |
dc.identifier.email | Choi, CW: hcchoi@hku.hk | - |
dc.identifier.email | So, TH: sth495@hku.hk | - |
dc.identifier.authority | Chiang, CL=rp02241 | - |
dc.identifier.authority | So, TH=rp01981 | - |
dc.description.nature | abstract | - |
dc.identifier.doi | 10.1093/annonc/mdx662 | - |
dc.identifier.hkuros | 286201 | - |
dc.identifier.hkuros | 303696 | - |
dc.identifier.volume | 28 | - |
dc.identifier.issue | Suppl. 10 | - |
dc.identifier.spage | x77, abstract no. 261O | - |
dc.identifier.epage | x77, abstract no. 261O | - |
dc.identifier.isi | WOS:000425626900270 | - |
dc.publisher.place | United Kingdom | - |
dc.identifier.issnl | 0923-7534 | - |