Alternating Cystoscopy with Bladder EpiCheck

Bladder cancer NMIBC surveillance cost model urinary markers

Journal

Bladder cancer (Amsterdam, Netherlands)
ISSN: 2352-3735
Titre abrégé: Bladder Cancer
Pays: Netherlands
ID NLM: 101668567

Informations de publication

Date de publication:
2021
Historique:
received: 22 03 2021
accepted: 15 05 2021
medline: 31 8 2021
pubmed: 31 8 2021
entrez: 12 7 2024
Statut: epublish

Résumé

Bladder cancer surveillance is invasive, intensive and costly. Patients with low grade intermediate risk non-muscle invasive bladder cancer (NMIBC) are at high risk of recurrence. The objective of this model is to compare the cost of a strategy to alternate surveillance with cystoscopy and a urine marker, Bladder EpiCheck, to standard surveillance. A decision tree model was built using TreeAge Pro Healthcare to compare standard surveillance (Standard) with a modified surveillance incorporating Bladder EpiCheck. The model was based on 2 years of surveillance. Outcomes were obtained from literature. Costs were obtained from US and 9 European countries. Sensitivity analyses were performed. The efficacy of the model was equivalent in terms of recurrence for each arm with median recurrence rate of 22%. When setting marker price at 200 local currency, the marker arm was less expensive in the USA, Netherlands, Switzerland, Belgium, Italy, Austria and UK by 154€ to 329£ per patient, for a 2-year period. Cost was higher in France, Spain, and Germany by 33-103€. Cost parity was achieved with marker price between 148€ and $421. Marker cost and specificity have the greatest impact on the overall model cost. A strategy alternating the urine marker Bladder EpiCheck with cystoscopy in the surveillance of patients with low grade intermediate risk bladder cancer is cost equivalent in the US and European countries when the marker is priced 148€ -$421, as a result of the marker's high specificity (86%). Prospective studies will be necessary to validate these findings.

Sections du résumé

BACKGROUND BACKGROUND
Bladder cancer surveillance is invasive, intensive and costly. Patients with low grade intermediate risk non-muscle invasive bladder cancer (NMIBC) are at high risk of recurrence.
OBJECTIVE OBJECTIVE
The objective of this model is to compare the cost of a strategy to alternate surveillance with cystoscopy and a urine marker, Bladder EpiCheck, to standard surveillance.
METHODS METHODS
A decision tree model was built using TreeAge Pro Healthcare to compare standard surveillance (Standard) with a modified surveillance incorporating Bladder EpiCheck. The model was based on 2 years of surveillance. Outcomes were obtained from literature. Costs were obtained from US and 9 European countries. Sensitivity analyses were performed.
RESULTS RESULTS
The efficacy of the model was equivalent in terms of recurrence for each arm with median recurrence rate of 22%. When setting marker price at 200 local currency, the marker arm was less expensive in the USA, Netherlands, Switzerland, Belgium, Italy, Austria and UK by 154€ to 329£ per patient, for a 2-year period. Cost was higher in France, Spain, and Germany by 33-103€. Cost parity was achieved with marker price between 148€ and $421. Marker cost and specificity have the greatest impact on the overall model cost.
CONCLUSIONS CONCLUSIONS
A strategy alternating the urine marker Bladder EpiCheck with cystoscopy in the surveillance of patients with low grade intermediate risk bladder cancer is cost equivalent in the US and European countries when the marker is priced 148€ -$421, as a result of the marker's high specificity (86%). Prospective studies will be necessary to validate these findings.

Identifiants

pubmed: 38993615
doi: 10.3233/BLC-211528
pii: BLC211528
pmc: PMC11181831
doi:

Types de publication

Journal Article

Langues

eng

Pagination

307-315

Informations de copyright

© 2021 – The authors. Published by IOS Press.

Déclaration de conflit d'intérêts

All authors are consultants for Nucleix Ltd (YL, GG, MM, JM, HM, FP, CP, MR, CS, SS, AW)

Auteurs

Yair Lotan (Y)

Department of Urology, UT Southwestern Medical Center, Dallas, TX, USA.

Georgios Gakis (G)

Department of Urology and Paediatric Urology, University Hospital of Würzburg, Würzburg, Germany.

Matteo Manfredi (M)

Department of Urology - University of Turin, San Luigi Gonzaga Hospital, Orbassano (TO), Italy.

Juan Morote (J)

Department of Urology, Vall d'Hebron University Hospital, Universitat Autònoma de Barcelona, Barcelona, Spain.

Hugh Mostafid (H)

Department of Urology, Royal Surrey County Hospital, Egerton Road, Guildford, Surrey, UK.

Francesco Porpiglia (F)

Department of Urology - University of Turin, San Luigi Gonzaga Hospital, Orbassano (TO), Italy.

Cedric Poyet (C)

Department of Urology, University Hospital Zürich, University of Zürich, Zürich, Switzerland.

Morgan Roupret (M)

Sorbonne University, GRC n°5, PREDICTIVE ONCO-URO, AP-HP, Urology, Pitié-Salpetriere Hospital, Paris, France.

Claude Schulman (C)

Clinic E. Cavell and University of Brussels, Brussels, Belgium.

Shahrokh F Shariat (SF)

Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Institute for Urology and Reproductive Health, I.M. Sechenov First Moscow State Medical University, Moscow, Russia.
European Association of Urology Research Foundation, Arnhem, The Netherlands.

Johannes Alfred Witjes (JA)

Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

Classifications MeSH