Abstract 2165P
Background
Monitoring symptoms and toxicities through the use of electronic objects (electronic patient-reported outcomes, ePRO) has been shown to improve overall survival and quality of life in several clinical trials in oncology. We intended to investigate the use of ePRO in France in 2022.
Methods
An electronic form was sent to pharmacists in 416 cancer departments. Data were collected from October 2022 to December 2022. Pharmacists were asked about their use of ePRO, funding, potential improvements, and barriers to implementation.
Results
We obtained a participation rate of 25% (114/416 cancer departments, 2 were excluded due to misunderstanding). Only 13% (n=15) use ePRO.
ePRO users mentioned potential improvements in the technology : implementation of the ePRO platform directly into the patient record and a desire to improve communication between professionals (n=5). Difficulties they encountered were mainly interoperability, which affects efficiency (n=5), and lack of human resources (n=3).
Of the 97 who do not use ePRO, 42% (n=41) are unaware of the existence of ePRO. 67% (n=65) of them would like to implement ePRO and hospital implementation is planned in 28% (n=27) of cancer departments. They describe possible difficulties due to lack of time to check patients' answers (74%, n=72), lack of human resources (67%, n=65), lack of financial resources (n=6, 6%), and digital literacy in elderly patients (5%, n=5).
Conclusions
A majority of cancer departments showed interest into ePROs. Two categories of improvements were identified : human resources to help with deployment, and better software to improve interoperability. The reimbursement of electronic monitoring starting in 2023 in France will encourage its incorporation in routine practice.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
2184TiP - Extensive cardiovascular characterization and follow-up of patients receiving immune checkpoint inhibitors: A prospective multicenter study
Presenter: Danielle Delombaerde
Session: Poster session 07
2185TiP - Belgian FORX trial: FOod interventions to Reduce immunotherapy toXicity
Presenter: Marthe Verhaert
Session: Poster session 07
2186P - KN046 in patients with thymic carcinoma: A prospective, single-arm, multi-centre, phase II study
Presenter: Wentao Fang
Session: Poster session 07
2187P - Efficacy and safety of gemcitabine as maintenance treatment in unresectable malignant pleural mesothelioma: A phase II randomized study
Presenter: Mohamed Emam Sobeih
Session: Poster session 07
2188P - First-line combination of toripalimab and chemotherapy in advanced thymic carcinoma: A prospective, single-arm, phase II trial
Presenter: hui'yang shi
Session: Poster session 07
2189P - Combining SBRT with GM-CSF and Peg-IFNα to induce abscopal effects in previously treated patients with stage IV thymic tumors
Presenter: Boyan Wang
Session: Poster session 07
2190P - First-line atezolizumab in combination with platinum etoposide in patients with metastatic lung large cell neuroendocrine carcinoma (LCNEC)
Presenter: Georgios Evangelou
Session: Poster session 07
2191P - Real-world outcomes of patients with malignant pleural mesothelioma (MPM) treated with combination nivolumab and ipilimumab in the first- or later line setting
Presenter: Sabine Schmid
Session: Poster session 07
2192P - Quality of life (QoL) of patients (pts) with advanced malignant pleural mesothelioma (aMPM) treated in a real-world setting
Presenter: Abhenil Mittal
Session: Poster session 07
2193P - Real-world evidence of the impact of immunotherapy (IT) on overall survival (OS) of patients (p) with malignant pleural mesothelioma (MPM) adjusted for tumor histology
Presenter: Susana Cedres Perez
Session: Poster session 07