Early follow-up of outpatients with oral anticancer therapy in the ONCORAL multidisciplinary community-hospital program

Author:

Lattard Claire1,Herledan Chloé12,Reverdy Thibaut3,Antherieu Gabriel4,Caffin Anne-Gaelle1,Cerfon Marie-Anne1,Maire Magali1,Rivat Marine1,France Stéphanie1,Ghesquières Hervé4,You Benoit23ORCID,Freyer Gilles23,Ranchon Florence12ORCID,Rioufol Catherine12ORCID

Affiliation:

1. Hospices Civils de Lyon, Groupement Hospitalier Sud, Unité de Pharmacie Clinique Oncologique , 69495 Pierre-Bénite , France

2. Université Lyon 1, EA 3738, CICLY , Lyon, 69921 OULLINS Cedex ,  France

3. Hospices Civils de Lyon, Groupement Hospitalier Sud, Unité d’Oncologie médicale , 69495 Pierre-Bénite , France

4. Hospices Civils de Lyon, Groupement Hospitalier Sud, Unité d’hématologie , 69495 Pierre-Bénite , France

Abstract

Abstract Background Healthcare professionals are faced with the new challenges of preventing and managing drug-related problems (DRPs) with oral anticancer therapy (OAT): side-effects, drug–drug interactions (DDIs), non-adherence, or medication errors. This study aims to assess the impact of ONCORAL, a real-life multidisciplinary care plan for cancer patients based on community and hospital follow-up, for the first OAT cycle. Methods A prospective cohort study was conducted between October 1, 2021 and October 1, 2022 including all outpatients starting OAT treatment. During the first OAT cycle, the program consists of 6 weekly scheduled face-to-face or phone consultations to prevent and manage DRPs. Nurse and pharmacist interventions (NPIs) are realized to optimize treatments (primary outcomes). Secondary outcomes included the relative dose intensity (RDI) of the first cycle. Results A total of 562 NPIs were performed by the ONCORAL team: that is, 87.1% of the 209 patients included, for a mean of 3.1 ± 2.2 NPIs/patient. NPIs-concerned DRPs detected by the nurse and pharmacist (346, 61.6%), symptoms and/or adverse effects reported as PROs by the patient or family (138, 24.6%), or pathway issues (78, 13.9%). Seventy-three DDIs were detected and managed during medication review, in a quarter of patients (n = 54/209), leading to the discontinuation of a daily concomitant medication in 30 cases. The mean RDI at the end of the first cycle, calculated for 209 patients, was 83.1 ± 23.9% (17.56-144.23). Conclusion In these ambulatory cancer patients, the interest in tailored monitoring of DRPs as a whole, including the prevention and management of drug interactions in addition to symptoms and adverse effects, is highlighted.

Publisher

Oxford University Press (OUP)

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