Related Experiment Video
Updated: May 28, 2026

Evaluating the Effectiveness of Cancer Drug Sensitization In Vitro and In Vivo
Published on: February 6, 2015
Development and Evaluation of a Web-Based App for Adverse Effect Management in Breast Cancer Patients Treated with
Julie Lemieux1, Isabelle Côté1, Martine Lemay1
1Centre des Maladies du Sein, CHU de Québec-Université Laval, Quebec City, QC G1S 4L8, Canada.
Abstract:
This pilot study (NCT05743686) evaluated the feasibility of a web-based application enabling patients with breast cancer (BC) receiving oral therapy to self-report and manage treatment-related adverse effects (AEs). Patients were enrolled between January and August 2023. Historical controls were used for comparison. Participants used the web-app to self-report AEs daily for 13 weeks, completed the PRO-CTCAE weekly, and completed a questionnaire assessing psychosocial precursor factors associated with treatment adherence. Some patients and healthcare professionals participated in semi-structured interviews. The study included 28 participants and 185 historical controls. Compared with controls, participants had fewer interactions with hospital pharmacists (0 [0-1] vs. 0 [0-7], p = 0.04), with no significant differences in the number of visits, hospitalizations, or modifications to treatment. Concordance between AEs reported via the web-app and PRO-CTCAE was 66.2%. No statistically significant changes were observed in psychosocial precursor factors of treatment adherence following the intervention (all p > 0.05). The qualitative data underscored the generally positive reception of the web-based application among both patients and healthcare professionals. In conclusion, in this small mixed-methods pilot study, monitoring oral cancer therapy-related adverse effects using the web-app was feasible and acceptable, and was associated with a lower frequency of telephone contacts with hospital pharmacists compared with historical usual care. These preliminary findings are exploratory and warrant confirmation in larger, prospectively designed studies.
Related Concept Videos
Therapeutic Drug Monitoring: Affecting Factors
Pharmacovigilance
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
Bioavailability Study Design: Healthy Subjects Versus Patients