Patient-reported Outcome Measurement and Reporting for Patients with Advanced Renal Cell Carcinoma: A Systematic Literature Review.


Journal

European urology
ISSN: 1873-7560
Titre abrégé: Eur Urol
Pays: Switzerland
ID NLM: 7512719

Informations de publication

Date de publication:
10 2023
Historique:
received: 31 03 2023
revised: 31 05 2023
accepted: 17 07 2023
medline: 18 9 2023
pubmed: 8 8 2023
entrez: 7 8 2023
Statut: ppublish

Résumé

In the oncology setting, patient-reported outcome measures (PROMs) provide important data that help to ensure patient-relevant endpoints are captured and reported. Use of this information for treatment decision-making by clinicians and patients in real-world settings is facilitated by consistent and transparent reporting of trial methods. To identify and compare PROMs used in advanced renal cell carcinoma (RCC) trials in terms of the rationale for the choice of measure, endpoint hierarchy (primary, secondary, exploratory), assessment time points, statistical methods, and statistical metrics for interpretation. A systematic literature review via searches of four online databases (2016-2021) and recent conference abstracts (2019-2021) identified 2616 articles, of which 33 were included in the review according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. Among the 33 clinical studies included, 19 different PROMs were identified: three kidney cancer-specific scales, two cancer-specific scales, two generic scales, and 12 symptom-specific scales. The endpoint hierarchy for patient reported outcome (PRO) assessment was reported in 42% of the studies; one study included PROs as a primary endpoint. Reporting of time points, minimal important differences, and statistical analyses was highly heterogeneous. A diverse range of PROMs have been included in clinical studies for patients with advanced/metastatic RCC. Prespecified analyses for PRO assessments were generally not stated, while analytical methods and reporting varied. An improvement in alignment across studies would better inform regulatory, market-access, reimbursement, and clinical decision-making to improve patient care. We reviewed how the impact of cancer therapies on health outcomes from the patient's point of view is being measured in clinical trials for kidney cancer. The techniques and reporting varied across trials. Standardisation of how these data are captured and reported may improve care and decision-making for patients with kidney cancer.

Identifiants

pubmed: 37550153
pii: S0302-2838(23)02971-8
doi: 10.1016/j.eururo.2023.07.006
pii:
doi:

Types de publication

Systematic Review Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

406-417

Informations de copyright

Copyright © 2023 European Association of Urology. Published by Elsevier B.V. All rights reserved.

Auteurs

Robert J Motzer (RJ)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA. Electronic address: motzerr@mskcc.org.

Pratik P Rane (PP)

Merck. & Co. Inc., Rahway, NJ, USA.

Todd L Saretsky (TL)

Merck. & Co. Inc., Rahway, NJ, USA.

Deepshikha Pawar (D)

Health Economics and Outcomes Research, Parexel, Mohali, India.

Allison Martin Nguyen (A)

Merck. & Co. Inc., Rahway, NJ, USA.

Murali Sundaram (M)

Merck. & Co. Inc., Rahway, NJ, USA.

Joseph Burgents (J)

Merck. & Co. Inc., Rahway, NJ, USA.

Rishabh Pandey (R)

Health Economics and Outcomes Research, Parexel, Bangalore, India.

Katja Rudell (K)

COA Science, Epidemiology and RW Sciences, Parexel, London, UK.

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Classifications MeSH