Author:
Tong Allison,Oberbauer Rainer,Bellini Maria Irene,Budde Klemens,Caskey Fergus J.,Dobbels Fabienne,Pengel Liset,Rostaing Lionel,Schneeberger Stefan,Naesens Maarten
Abstract
Patient-reported outcomes (PROs) that assess individuals’ perceptions of life participation, medication adherence, disease symptoms, and therapy side effects are extremely relevant in the context of kidney transplantation. All PROs are potentially suitable as primary or secondary endpoints in interventional trials that aim to improve outcomes for transplant recipients. Using PRO measures (PROMs) in clinical trials facilitates assessment of the patient’s perspective of their health, but few measures have been developed and evaluated in kidney transplant recipients; robust methodologies, which use validated instruments and established frameworks for reporting, are essential. Establishing a core PROM for life participation in kidney transplant recipients is a critically important need, which is being developed and validated by the Standardized Outcomes in Nephrology (SONG)-Tx Initiative. Measures involving electronic medication packaging and smart technologies are gaining traction for monitoring adherence, and could provide more robust information than questionnaires, interviews, and scales. This article summarizes information on PROs and PROMs that was included in a Broad Scientific Advice request on clinical trial design and endpoints in kidney transplantation. This request was submitted to the European Medicines Agency (EMA) by the European Society for Organ Transplantation in 2016. Following modifications, the EMA provided its recommendations in late 2020.
Reference72 articles.
1. Role of Patient-Reported Outcomes and Other Efficacy Endpoints in the Drug Approval Process in Europe (2008-2012);Bansal;J. Epidemiol Global Health,2015
2. EMEA/CHMP/EWP/139391/2004. Reflection Paper on the Regulatory Guidance for the Use of Health-Related Quality of Life (HRQL) Measures in the Evaluation of Medicinal Products2022
3. Guidance for Industry: Patient-Reported Outcome Measures: Use in Medical Product Development to Support Labeling Claims: Draft Guidance;Health Qual Life Outcomes,2006
4. The SPIRIT-PRO Group. Guidelines for Inclusion of Patient-Reported Outcomes in Clinical Trial Protocols: The SPIRIT-PRO Extension;Calvert;JAMA,2018
5. Guideline on Clinical Investigation of Medicinal Products for the Treatment of Rheumatoid Arthritis (CPMP/EWP/556/95)2022
Cited by
17 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献