» Articles » PMID: 38367968

Cost-effectiveness of the ONCORAL Multidisciplinary Programme for the Management of Outpatients Taking Oral Anticancer Agents at Risk of Drug-related Event: Protocol for a Pragmatic Randomised Controlled Study

Overview
Journal BMJ Open
Specialty General Medicine
Date 2024 Feb 17
PMID 38367968
Authors
Affiliations
Soon will be listed here.
Abstract

Introduction: The development of oral anticancer agents (OAA) has profoundly changed cancer care, leading patients to manage their chemotherapy treatment on an outpatient basis. The prevention of iatrogenic effects of OAA remains a major concern, especially since their side effects are not less serious than those of intravenous chemotherapy. The ONCORAL programme was set up to secure the management of OAA in cancer patients followed at the Lyon University Hospital. This multidisciplinary programme involves hospital pharmacists, nurses, oncologists, and haematologists, as well as community health professionals. Given the economic stakes that this programme entails for the health system, a medico-economic study was designed.

Methods And Analysis: This is a prospective controlled study, with individual open-label randomisation. A total of 216 outpatients treated with OAA and at risk of developing a drug-related iatrogenic event, will be randomised (2:1) to undergo follow-up in the ONCORAL programme or usual care. The primary outcome will be the estimation of the incremental cost-effectiveness ratio (difference in total costs per quality adjusted life years gained) at 12 months between the two groups. The secondary outcomes will be evaluation of OAA management consequences (relative-dose intensity, adherence, adverse drug events, drug-drug interactions, and proven medication errors), evaluation of overall survival and cancer-related quality of life, and patient-reported outcomes in relation to the treatment. A budget impact analysis will be implemented. Patient and health professional satisfaction regarding the ONCORAL programme will be measured.

Ethics And Dissemination: Approval to conduct this study was obtained from an Ethics Committee () in October 2019, and from the French data protection agency (), according to the French Law. Trial results will be disseminated at clinical conferences and published in peer-reviewed journals.

Trial Registration: NCT03660670.

References
1.
Ruiz M, Pardo A, Rejas J, Soto J, Villasante F, Aranguren J . Development and validation of the "Treatment Satisfaction with Medicines Questionnaire" (SATMED-Q). Value Health. 2008; 11(5):913-26. DOI: 10.1111/j.1524-4733.2008.00323.x. View

2.
Liu S, Kurzrock R . Understanding Toxicities of Targeted Agents: Implications for Anti-tumor Activity and Management. Semin Oncol. 2015; 42(6):863-75. DOI: 10.1053/j.seminoncol.2015.09.032. View

3.
Liu G, Franssen E, Fitch M, Warner E . Patient preferences for oral versus intravenous palliative chemotherapy. J Clin Oncol. 1997; 15(1):110-5. DOI: 10.1200/JCO.1997.15.1.110. View

4.
Sidani S, Doran D . Development and Validation of a Self-Care Ability Measure. Can J Nurs Res. 2018; 46(1):11-25. DOI: 10.1177/084456211404600103. View

5.
ONeill V, Twelves C . Oral cancer treatment: developments in chemotherapy and beyond. Br J Cancer. 2002; 87(9):933-7. PMC: 2364332. DOI: 10.1038/sj.bjc.6600591. View