Understanding the Patient Journey: Barriers, Facilitators, and Expectations in Joining a Chemotherapy De-escalation Trial Among Premenopausal Patients with Breast Cancer

Background: De-escalation trials aim to balance clinical outcomes and quality of life (QoL), especially for premenopausal women with early breast cancer (BC), who often experience a greater treatment burden affecting their physical and psychosocial wellbeing.We sought to understand their patient journey-barriers, facilitators, and expectations-when joining de-escalation trials to inform patient-centered design and implementation.Methods: OPTIMA-YOUNG, an EU-co-funded international trial, investigates a genomic assay-guided approach to de-escalate chemotherapy in premenopausal patients with early-stage hormone receptor (HR)+ BC.A Co-creation Board of patients and healthcare professionals (HCPs) ensured stakeholder involvement throughout the trial.Focus groups (FGs) explored decision-making, needs, and QoL priorities related to joining a de-escalation clinical trial.Discussions were recorded, transcribed, anonymized, and analyzed using MAXQDA software.Results: The three FGs included 20 participants (11 patients, 9 HCPs) from 14 countries.Three themes emerged: 1) emotional and cognitive responses to BC diagnosis/treatment; 2) environmental, HCP, and social influences on choices; 3) coping with side effects and QoL challenges.Barriers to joining a de-escalation trial included limited emotional support at diagnosis, cross-country variations in shared decisionmaking, poor communication on long-term side effects, fear of recurrence, and HCPs' tendency to overtreat younger patients.Developing training for patients and HCPs was seen essential for improving communication, shared decision-making skills, and enhancing symptom management and QoL.Conclusions: This pre-implementation study identified factors at the patient, HCP, and system levels that, if addressed, could improve the trial experience.Insights helped refine the OPTIMA-YOUNG protocol and implementation plan and may inform future deescalation trials.

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Journal
The Breast
Published
2026-03-01
DOI
https://doi.org/10.1016/j.breast.2026.104770
Primary Topic
Breast Cancer Treatment Studies
Type
article
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article

Understanding the Patient Journey: Barriers, Facilitators, and Expectations in Joining a Chemotherapy De-escalation Trial Among Premenopausal Patients with Breast Cancer

Iain R. Macpherson, Isabelle Merckaert, Petya Zyumbileva, Maria Alice Franzoi et al.
The Breast
Breast Cancer Treatment Studies
article

Understanding the Patient Journey: Barriers, Facilitators, and Expectations in Joining a Chemotherapy De-escalation Trial Among Premenopausal Patients with Breast Cancer

Iain R. Macpherson, Isabelle Merckaert, Petya Zyumbileva, Maria Alice Franzoi, Maria Dutarte, Enrico Tricanico, Aure Vanhecke, Tanja Spanic, Elise Martin, Emma Gillanders, Sarra El-Abed, Marzia Zambon, Janet Dunn, Carmela Caballero, Ines Vaz-Luis
article en

Abstract

Background: De-escalation trials aim to balance clinical outcomes and quality of life (QoL), especially for premenopausal women with early breast cancer (BC), who often experience a greater treatment burden affecting their physical and psychosocial wellbeing.We sought to understand their patient journey-barriers, facilitators, and expectations-when joining de-escalation trials to inform patient-centered design and implementation.Methods: OPTIMA-YOUNG, an EU-co-funded international trial, investigates a genomic assay-guided approach to de-escalate chemotherapy in premenopausal patients with early-stage hormone receptor (HR)+ BC.A Co-creation Board of patients and healthcare professionals (HCPs) ensured stakeholder involvement throughout the trial.Focus groups (FGs) explored decision-making, needs, and QoL priorities related to joining a de-escalation clinical trial.Discussions were recorded, transcribed, anonymized, and analyzed using MAXQDA software.Results: The three FGs included 20 participants (11 patients, 9 HCPs) from 14 countries.Three themes emerged: 1) emotional and cognitive responses to BC diagnosis/treatment; 2) environmental, HCP, and social influences on choices; 3) coping with side effects and QoL challenges.Barriers to joining a de-escalation trial included limited emotional support at diagnosis, cross-country variations in shared decisionmaking, poor communication on long-term side effects, fear of recurrence, and HCPs' tendency to overtreat younger patients.Developing training for patients and HCPs was seen essential for improving communication, shared decision-making skills, and enhancing symptom management and QoL.Conclusions: This pre-implementation study identified factors at the patient, HCP, and system levels that, if addressed, could improve the trial experience.Insights helped refine the OPTIMA-YOUNG protocol and implementation plan and may inform future deescalation trials.

The Breast
Inserm (FR), Université Paris-Saclay (FR), Alma Mater Europaea (SI), Institut Jules Bordet (BE), Institut Gustave Roussy (FR), Breast International Group (BE), University of Warwick (GB), Laboratoire Pluridisciplinaire de Recherche en Ingénierie des Systèmes, Mécanique et Energétique (FR), Centre de recherche en Epidémiologie et Santé des Populations (FR), UniCancer Group (FR), Europa Donna (IT), The Patients Association (GB), Charité - Universitätsmedizin Berlin (DE), University of Glasgow (GB)
Good health and well-being
Openalex Percentile: Top 9%
Breast Cancer Treatment Studies
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