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Patients' Preferences for Adjuvant Endocrine Therapy in Early Breast Cancer

Evaluation of Endocrine Therapy and Patients Preferences in Early Breast Cancer - Patients' Preferences for Adjuvant Endocrine Therapy in Early Breast Cancer.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03939156
Acronym
ELENA
Enrollment
450
Registered
2019-05-06
Start date
2018-06-05
Completion date
2023-12-31
Last updated
2023-06-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer, Endocrine Breast Diseases

Keywords

adjuvant endocrine therapy, patient's preferences

Brief summary

Preference studies reveal how individuals trade-off the potential benefits, harms and inconveniences of a treatment by determining the minimum benefits they judge sufficient to make the treatment worthwhile. They are especially relevant to adjuvant therapies where individuals must weigh up modest survival benefits only realized in time by no recurrence of their cancer with side effects predominantly experienced whilst on the treatment. Previously it was reported, for example, that over 50% of women who had adjuvant chemotherapy for early breast cancer judged a 1% improvement in 5 year survival rates sufficient to make it worthwhile. Larger survival benefits were required for longer duration adjuvant hormonal therapy where over 50% of women required at least 5% improvement in 5 year survival rates to make it worthwhile.

Detailed description

The endocrine therapy is generally proposed to all patients with endocrine positive early breast cancer to reduce the risk of recurrence and death. Moreover several data support that the prolongation of hormonal therapy (i.e. 10 years of hormonal treatment) is associated with statistical improved outcome. In order to achieve the benefit related to hormonal therapy all women have to be treated despite the fact that the data and analyses are unable to differentiate as to whether a small prolongation in survival accrues to all women treated or a few patients survive who would otherwise have died. Moreover the hormonal therapy is associated with side effects that may impact the quality of life of the patients. Patients are more likely to accept treatment on the basis of presented relative rather than absolute risks and so the question arises as to whether unrealistic improvements in outcome are expected by patients. The interviews with patients in the proposed trial will elicit the expected gains both in terms of survival and life years and will be able to assess the proportion of patients who considered an improvement of realistic size was sufficient to justify the treatment and the prolongation of the treatment. Several studies showed that choices are guided by the personal attitude to react and adapt to traumatic events, individual resilience. It is important therefore to consider also the influence of these factors on the patients' treatment preferences. For this reason, besides the elicitation of preferences, resilience and reaction to traumatic events will be assessed thorough validated questionnaires.

Interventions

Completion of questionnaires at the time of study entry

Sponsors

European Institute of Oncology
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Women candidate to adjuvant hormonal therapy for breast cancer before the start of therapy * Women who are receiving hormonal therapy (within 1 year from beginning) * Women who are receiving hormonal therapy (who had receive at least 4 or 5 or 6 years of hormonal therapy) * Patients who underwent to radical surgery for breast cancer * Patients who have received neoadjuvant or adjuvant chemotherapy are also eligible * Hormonal receptors positive breast cancer (ER and or PgR \>1%) * Sufficient literacy in Italian to complete the questionnaires.

Exclusion criteria

* Patients who had received at least 1 year and no more than 3 years of hormonal therapy * Patients who are receiving hormonal therapy (who had receive 7 years or more of hormonal therapy)

Design outcomes

Primary

MeasureTime frameDescription
Percentage of risk reduction needed to consider endocrine therapy worthwhile1 weekRisk reduction will be evaluated in the 40% and 20% 5 years risk scenarios
Number of years gain needed to consider ET worthwhile1 weekProlonged survival time gain will be evaluated in the 5-yr and 15-yr survival scenarios

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026