Literature DB >> 27256016

Cost-effectiveness of zoledronic acid and strontium-89 as bone protecting treatments in addition to chemotherapy in patients with metastatic castrate-refractory prostate cancer: results from the TRAPEZE trial (ISRCTN 12808747).

Lazaros Andronis1, Ilias Goranitis1, Sarah Pirrie2, Ann Pope2, Darren Barton2, Stuart Collins3, Adam Daunton4, Duncan McLaren5, Joe M O'Sullivan6, Chris Parker7, Emilio Porfiri4, John Staffurth8, Andrew Stanley9, James Wylie10, Sharon Beesley11, Alison Birtle12, Janet E Brown13, Prabir Chakraborti14, Syed A Hussain15, J Martin Russell16, Lucinda J Billingham2, Nicholas D James4.   

Abstract

OBJECTIVE: To evaluate the cost-effectiveness of adding zoledronic acid or strontium-89 to standard docetaxel chemotherapy for patients with castrate-refractory prostate cancer (CRPC). PATIENTS AND METHODS: Data on resource use and quality of life for 707 patients collected prospectively in the TRAPEZE 2 × 2 factorial randomised trial (ISRCTN 12808747) were used to assess the cost-effectiveness of i) zoledronic acid versus no zoledronic acid (ZA vs. no ZA), and ii) strontium-89 versus no strontium-89 (Sr89 vs. no Sr89). Costs were estimated from the perspective of the National Health Service in the UK and included expenditures for trial treatments, concomitant medications, and use of related hospital and primary care services. Quality-adjusted life-years (QALYs) were calculated according to patients' responses to the generic EuroQol EQ-5D-3L instrument, which evaluates health status. Results are expressed as incremental cost-effectiveness ratios (ICERs) and cost-effectiveness acceptability curves.
RESULTS: The per-patient cost for ZA was £12 667, £251 higher than the equivalent cost in the no ZA group. Patients in the ZA group had on average 0.03 QALYs more than their counterparts in no ZA group. The ICER for this comparison was £8 005. Sr89 was associated with a cost of £13 230, £1365 higher than no Sr89, and a gain of 0.08 QALYs compared to no Sr89. The ICER for Sr89 was £16 884. The probabilities of ZA and Sr89 being cost-effective were 0.64 and 0.60, respectively.
CONCLUSIONS: The addition of bone-targeting treatments to standard chemotherapy led to a small improvement in QALYs for a modest increase in cost (or cost-savings). ZA and Sr89 resulted in ICERs below conventional willingness-to-pay per QALY thresholds, suggesting that their addition to chemotherapy may represent a cost-effective use of resources.
© 2016 The Authors BJU International published by John Wiley & Sons Ltd on behalf of BJU International.

Entities:  

Keywords:  Sr89; bone protecting treatments; castrate-refractory prostate cancer; cost-effectiveness analysis; quality of life; zoledronic acid

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Substances:

Year:  2016        PMID: 27256016     DOI: 10.1111/bju.13549

Source DB:  PubMed          Journal:  BJU Int        ISSN: 1464-4096            Impact factor:   5.588


  5 in total

Review 1.  Treatments for Metastatic Prostate Cancer (mPC): A Review of Costing Evidence.

Authors:  Jan Norum; Carsten Nieder
Journal:  Pharmacoeconomics       Date:  2017-12       Impact factor: 4.981

Review 2.  Bisphosphonates for advanced prostate cancer.

Authors:  Sascha Macherey; Ina Monsef; Franziska Jahn; Karin Jordan; Kwok Keung Yuen; Axel Heidenreich; Nicole Skoetz
Journal:  Cochrane Database Syst Rev       Date:  2017-12-26

3.  Cost-Effectiveness of Treatments for the Management of Bone Metastases: A Systematic Literature Review.

Authors:  Lazaros Andronis; Ilias Goranitis; Sue Bayliss; Rui Duarte
Journal:  Pharmacoeconomics       Date:  2018-03       Impact factor: 4.981

4.  Bisphosphonates or RANK-ligand-inhibitors for men with prostate cancer and bone metastases: a network meta-analysis.

Authors:  Tina Jakob; Yonas Mehari Tesfamariam; Sascha Macherey; Kathrin Kuhr; Anne Adams; Ina Monsef; Axel Heidenreich; Nicole Skoetz
Journal:  Cochrane Database Syst Rev       Date:  2020-12-03

5.  Cost-effectiveness analyses and cost analyses in castration-resistant prostate cancer: A systematic review.

Authors:  Thomas Grochtdreis; Hans-Helmut König; Alexander Dobruschkin; Gunhild von Amsberg; Judith Dams
Journal:  PLoS One       Date:  2018-12-05       Impact factor: 3.240

  5 in total

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