Cost-effectiveness of Pembrolizumab for Patients with Advanced, Unresectable, or Metastatic Urothelial Cancer Ineligible for Cisplatin-based Therapy.


Journal

European urology oncology
ISSN: 2588-9311
Titre abrégé: Eur Urol Oncol
Pays: Netherlands
ID NLM: 101724904

Informations de publication

Date de publication:
09 2019
Historique:
received: 14 05 2018
revised: 12 09 2018
accepted: 19 09 2018
pubmed: 15 8 2019
medline: 20 6 2020
entrez: 15 8 2019
Statut: ppublish

Résumé

There is an unmet need for effective therapies for patients with advanced or metastatic urothelial cancer who cannot tolerate cisplatin-based chemotherapy. Cisplatin-ineligible patients experience a high frequency of adverse events from the most commonly used standard of care treatment, carboplatin plus gemcitabine, or alternative treatment with gemcitabine monotherapy. Pembrolizumab is a potent, highly selective humanised monoclonal antibody that releases checkpoint inhibition of the immune response system, and provides a new alternative for these patients. To assess the cost-effectiveness of pembrolizumab for first-line treatment of urothelial carcinoma ineligible for cisplatin-based therapy in patients with strongly PD-L1-positive tumours in Sweden. Parametric survival curves were fitted to overall survival, progression-free survival, and time on treatment data from KEYNOTE-052 to extrapolate clinical outcomes. A simulated treatment comparison and a network meta-analysis were conducted to estimate the comparative efficacy of pembrolizumab versus carboplatin plus gemcitabine and gemcitabine monotherapy. EQ-5D data from KEYNOTE-052 were used to estimate utility, while resource use and cost inputs were estimated using Swedish regional pricing lists and clinician opinion. The model reported costs, life years, and quality-adjusted life years (QALYs), and results were tested using deterministic and probabilistic sensitivity analysis. We estimated that pembrolizumab would improve survival by 2.11 and 2.16 years and increase QALYs by 1.71 and 1.75 compared to carboplatin plus gemcitabine and gemcitabine monotherapy, respectively. Pembrolizumab was associated with a cost increase of €90520 versus carboplatin plus gemcitabine and €95055 versus gemcitabine, with corresponding incremental cost-effectiveness ratios of €53055/QALY and €54415/QALY. At a willingness-to-pay threshold of €100000/QALY, pembrolizumab is a cost-effective treatment versus carboplatin plus gemcitabine and versus gemcitabine. This is the first analysis to show that pembrolizumab is a cost-effective option for first-line treatment of cisplatin-ineligible patients with locally advanced or metastatic urothelial carcinoma in Sweden.

Sections du résumé

BACKGROUND
There is an unmet need for effective therapies for patients with advanced or metastatic urothelial cancer who cannot tolerate cisplatin-based chemotherapy. Cisplatin-ineligible patients experience a high frequency of adverse events from the most commonly used standard of care treatment, carboplatin plus gemcitabine, or alternative treatment with gemcitabine monotherapy. Pembrolizumab is a potent, highly selective humanised monoclonal antibody that releases checkpoint inhibition of the immune response system, and provides a new alternative for these patients.
OBJECTIVE
To assess the cost-effectiveness of pembrolizumab for first-line treatment of urothelial carcinoma ineligible for cisplatin-based therapy in patients with strongly PD-L1-positive tumours in Sweden.
DESIGN, SETTING, AND PARTICIPANTS
Parametric survival curves were fitted to overall survival, progression-free survival, and time on treatment data from KEYNOTE-052 to extrapolate clinical outcomes. A simulated treatment comparison and a network meta-analysis were conducted to estimate the comparative efficacy of pembrolizumab versus carboplatin plus gemcitabine and gemcitabine monotherapy. EQ-5D data from KEYNOTE-052 were used to estimate utility, while resource use and cost inputs were estimated using Swedish regional pricing lists and clinician opinion.
OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS
The model reported costs, life years, and quality-adjusted life years (QALYs), and results were tested using deterministic and probabilistic sensitivity analysis.
RESULTS AND LIMITATIONS
We estimated that pembrolizumab would improve survival by 2.11 and 2.16 years and increase QALYs by 1.71 and 1.75 compared to carboplatin plus gemcitabine and gemcitabine monotherapy, respectively. Pembrolizumab was associated with a cost increase of €90520 versus carboplatin plus gemcitabine and €95055 versus gemcitabine, with corresponding incremental cost-effectiveness ratios of €53055/QALY and €54415/QALY.
CONCLUSIONS
At a willingness-to-pay threshold of €100000/QALY, pembrolizumab is a cost-effective treatment versus carboplatin plus gemcitabine and versus gemcitabine.
PATIENT SUMMARY
This is the first analysis to show that pembrolizumab is a cost-effective option for first-line treatment of cisplatin-ineligible patients with locally advanced or metastatic urothelial carcinoma in Sweden.

Identifiants

pubmed: 31412011
pii: S2588-9311(18)30169-X
doi: 10.1016/j.euo.2018.09.009
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Antineoplastic Agents, Immunological 0
B7-H1 Antigen 0
CD274 protein, human 0
Deoxycytidine 0W860991D6
Carboplatin BG3F62OND5
pembrolizumab DPT0O3T46P
Cisplatin Q20Q21Q62J
Gemcitabine 0

Types de publication

Comparative Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

565-571

Informations de copyright

Copyright © 2018 Merck Sharp & Dohme Corp and The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

Karl Patterson (K)

BresMed Health Solutions, Sheffield, UK.

Vimalanand Prabhu (V)

Center for Observational & Real-world Evidence, Merck & Co. Inc., Kenilworth, NJ, USA.

Ruifeng Xu (R)

Center for Observational & Real-world Evidence, Merck & Co. Inc., Kenilworth, NJ, USA.

Haojie Li (H)

Center for Observational & Real-world Evidence, Merck & Co. Inc., Kenilworth, NJ, USA.

Yang Meng (Y)

BresMed Health Solutions, Sheffield, UK.

Natalie Zarabi (N)

MSD, Stockholm, Sweden.

Yichen Zhong (Y)

Center for Observational & Real-world Evidence, Merck & Co. Inc., Kenilworth, NJ, USA. Electronic address: yichen.zhong@merck.com.

Rachael Batteson (R)

BresMed Health Solutions, Sheffield, UK.

James Pellissier (J)

Center for Observational & Real-world Evidence, Merck & Co. Inc., Kenilworth, NJ, USA.

Stephen Keefe (S)

Center for Observational & Real-world Evidence, Merck & Co. Inc., Kenilworth, NJ, USA.

Petros Grivas (P)

Department of Medicine, Division of Oncology, University of Washington, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.

Ronald de Wit (R)

Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

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Classifications MeSH