نبذة مختصرة : Background: In France, breast cancer is the most commonly diagnosed cancer and the leading cause of cancer-related death among women. For around one-third of women with hormone receptor-positive breast cancer, extending adjuvant endocrine therapy (AET) beyond the initial 5 years is now recommended to reduce the risk of recurrence and mortality. While weighing benefits against potential side effects is essential, little is known about how women seek information about extended AET or how they experience this extension.
Objective: This study aimed to explore, through online forums, women's unmet information needs, the factors influencing their decision-making around extended AET, and the needs and expectations they share throughout the treatment journey.
Methods: A qualitative content analysis was conducted using data from 5 French online forums over a 10-year period. We used a nonparticipant observational approach to identify relevant posts and gain a deeper understanding of forum dynamics related to extended AET. Data were collected in March 2025. After applying inclusion and exclusion criteria, 188 messages posted by 105 women were selected. A netnographic approach, derived from ethnography and suited to exploratory research, was used in conjunction with Braun and Clarke's 6-phase framework for thematic analysis, integrating both inductive (narrative-based) and deductive (literature-informed) approaches.
Results: Our findings showed that women turned to forums to seek information about extended AET from both medical and nonexpert sources. However, they often reported difficulties in interpreting complex or inconsistent information. Understanding and acceptance of treatment extension were influenced by the timing and manner of information disclosure. Three decision-making patterns were identified: (1) acceptance, (2) hesitation, and (3) refusal, which could shift over time, shaped by factors such as fear of recurrence, side effect experience and management, trust in treatment effectiveness, interactions with health care professionals, and life changes. Some women on extended AET shared resilient and encouraging experiences, providing reassurance and practical strategies for coping with side effects.
Conclusions: Online forums offer valuable insights into women's experiences, unmet information needs, uncertainties, and coping strategies surrounding extended AET, contributing to addressing a gap in knowledge on how women perceive and manage long-term treatment. Providing clear, accessible information and tailored communication tools, especially on benefit-risk balance and side effects management, at the time of prescription and at key points along the care pathway, may support informed decision-making, improve treatment adherence, maintain quality of life, and offer reassurance. With growing numbers of women in long-term treatment, enhanced coordination between primary care and hospital services, including follow-up by trained general practitioners and gynecologists in collaboration with cancer centers, may help ensure continuity of care and comprehensive support.
(© Geraldine Cazorla, Lorene Seguin, Magali Provansal, Sandrine De Montgolfier, Julien Mancini. Originally published in the Journal of Medical Internet Research (https://www.jmir.org).)
Processing Request
No Comments.