search
Back to results

Quality of Life and Psychological Vulnerability in Patients With RH+ Metastatic Breast Cancer (EPOCA)

Primary Purpose

Metastatic Breast Cancer, Positive Hormonal Receptors

Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Quality of life in metastatic BC
Sponsored by
Institut Cancerologie de l'Ouest
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Metastatic Breast Cancer focused on measuring Quality of Life, Psychological vulnerability

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Histologically confirmed diagnosis of invasive breast cancer (=infiltrant). NB: Mixed histologies are allowed
  2. Adult women (≥ 18 years),
  3. Positive hormonal receptors (Estrogen receptors and/or Progesterone receptors ≥10%) and HER2 negative
  4. Patient in need of a 1st metastatic treatment line NB: Patients may have received prior treatment for their cancer, but not for their metastatic disease.
  5. Performance status ≤ 1 (world health organization)
  6. Patients affiliated to a Social Security,
  7. Obtaining the patient's signed written consent

Exclusion Criteria:

  1. Patient with non-metastatic breast cancer,
  2. man
  3. Negative hormonal receptors or HER2 positive
  4. Psychiatric history with specialist diagnosis
  5. Pregnant or nursing patient
  6. Patients who cannot be followed regularly for psychological reasons (cognitive problems preventing completion of questionnaires), or because of geographical remoteness.
  7. Person deprived of liberty or adult under guardianship

Sites / Locations

  • Ico Angers
  • Ico Nantes

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

quality of life in metastatic BC

Arm Description

Patients benefit from a longitudinal follow-up determined according to the treatments. Each type of treatment has its own schedule based on medical consultation times. At each change of treatment, from chemotherapy to hormone therapy or vice versa, the assessment times are determined according to the nature of the treatment. The rhythm of the evaluation visits will therefore be defined by the doctor, according to the habits of the centre. The evaluation times used to collect the questionnaires (QLQ-C30, BR23, PDS, STAI, BDI II).

Outcomes

Primary Outcome Measures

Change from baseline quality of life during breast cancer treatment
quality of life assessed using QLQ-C30 Questionnaire
Change from baseline psychological vulnerability during breast cancer treatment
Psychological vulnerability assessed using STAI questionnaire
Change from baseline quality of life during breast cancer treatment
quality of life assessed using BR23 Questionnaire
Change from baseline psychological vulnerability during breast cancer treatment
Psychological vulnerability assessed using Psychological distress scale. The scale represents a means of assessing the psychological state of patients. The scale measures 10 cm. The patients will have to put a cross on the line at the place which corresponds best to their psychological state of the past week. 0 indicates no distress and 10 very important distress.
Change from baseline psychological vulnerability during breast cancer treatment
Psychological vulnerability assessed using BDI-II questionnaire

Secondary Outcome Measures

number of therapeutic class treatment prescribed during breast cancer treatment
The therapeutic strategy is modified in case of progression: chemotherapy and/or hormonotherapy. This change in treatment can affect the quality of life and psychological vulnerability of patients. The number of therapeutic classes prescribed in this way will make it possible to describe their impact over time on patients' quality of life and psychological vulnerability.

Full Information

First Posted
August 8, 2018
Last Updated
December 26, 2022
Sponsor
Institut Cancerologie de l'Ouest
search

1. Study Identification

Unique Protocol Identification Number
NCT03636776
Brief Title
Quality of Life and Psychological Vulnerability in Patients With RH+ Metastatic Breast Cancer
Acronym
EPOCA
Official Title
Prospective Study to Assess Quality of Life and Psychological Vulnerability in Patients With Metastatic Breast Cancer RH+
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Terminated
Why Stopped
The sponsor has set up a secondary competitive study concerning the same population and whose secondary objectives are the same as those of the EPOCA study with the same endpoints.
Study Start Date
December 29, 2016 (Actual)
Primary Completion Date
January 11, 2022 (Actual)
Study Completion Date
January 11, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institut Cancerologie de l'Ouest

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Metastatic breast cancer (MBC) is a dark prognostic disease with survival at 5 years of less than 20% and a median survival of 24 to 30 months after diagnosis of metastasis. Thus, metastatic diagnosis can be expected to have a different impact on the quality of life of patients in early and advanced stages. However, MBC benefits from therapeutics that improve patients' quality of life and even improve overall survival. The main objectives of this prospective study are : to evaluate the evolution over time of the quality of life of patients treated for positive hormonal receptors (RH+) metastatic breast cancer, according to the therapeutic class ; to evaluate the psychological vulnerability of these patients since the announcement of their metastatic diagnosis and during their treatments. Finally, when interviewing oncologists, to know the factors involved in a treatment change decision process for the same patient.
Detailed Description
Studying quality of life over time in patients followed for metastatic breast cancer will identify when a person may feel most vulnerable in their experience of the disease and treatment. A specific and adapted support can thus be set up throughout the disease, from the diagnosis and during the different phases of treatment. Patients will benefit from a longitudinal follow-up determined according to the treatments. For example : Chemotherapy : After the first assessment time at 1 month from diagnosis, patients receiving chemotherapy treatment are seen every 3 months. Hormone therapy : After the first assessment time at 1 month from diagnosis, patients receiving hormone therapy are seen every 2 months. Each type of treatment has its own schedule based on medical consultation times. At each change of treatment, from chemotherapy to hormone therapy or vice versa, the assessment times are determined according to the nature of the treatment. The rhythm of the evaluation visits will therefore be defined by the doctor, according to the habits of the centre. Patients will complete an end of study visit 3 years after inclusion Quality of Life and Psychological vulnerability will be assessed through questionnaires : QLQ-C30 explores 5 functional scales (physical, social, psychological, cognitive functioning, daily activities) and 1 scale of health status and overall quality of life. It allows a detailed analysis of symptoms related to the disease and its treatment (fatigue, nausea/vomiting, pain, dyspnea, loss of appetite, sleep disturbance, constipation and diarrhea) as well as the financial impact for the patient. BR23 : specific questionnaire for breast cancer validated in French Psychological distress scale (PDS) State Trait Anxiety Inventory (STAI) : Assesses the feelings of apprehension, tension, nervousness and worry that the subject feels at the time of the anxiogenic or endangerment situation. This questionnaire is therefore an indicator of transient changes in anxiety caused by aversive or therapeutic situations. Beck Depression Inventory (BDI II) : assesses the severity of depression.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metastatic Breast Cancer, Positive Hormonal Receptors
Keywords
Quality of Life, Psychological vulnerability

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
quality of life in metastatic BC
Arm Type
Experimental
Arm Description
Patients benefit from a longitudinal follow-up determined according to the treatments. Each type of treatment has its own schedule based on medical consultation times. At each change of treatment, from chemotherapy to hormone therapy or vice versa, the assessment times are determined according to the nature of the treatment. The rhythm of the evaluation visits will therefore be defined by the doctor, according to the habits of the centre. The evaluation times used to collect the questionnaires (QLQ-C30, BR23, PDS, STAI, BDI II).
Intervention Type
Other
Intervention Name(s)
Quality of life in metastatic BC
Intervention Description
1 month after metastatic stage diagnosis, patients complete their 1st therapeutic sequence evaluation visit (T1) within the recommended standard time frames. If the disease remains stable or if a response to treatment is observed then patients continue their follow-up in the same therapeutic sequence (T1). If progression occurs, treatment is modified and patients move on to the next therapeutic sequence (T2). And so on as many times as necessary. Before each evaluation visit with investigator, patients complete the questionnaires QLQ-C30, BR23, STAI, BDI II
Primary Outcome Measure Information:
Title
Change from baseline quality of life during breast cancer treatment
Description
quality of life assessed using QLQ-C30 Questionnaire
Time Frame
3 years
Title
Change from baseline psychological vulnerability during breast cancer treatment
Description
Psychological vulnerability assessed using STAI questionnaire
Time Frame
3 years
Title
Change from baseline quality of life during breast cancer treatment
Description
quality of life assessed using BR23 Questionnaire
Time Frame
3 years
Title
Change from baseline psychological vulnerability during breast cancer treatment
Description
Psychological vulnerability assessed using Psychological distress scale. The scale represents a means of assessing the psychological state of patients. The scale measures 10 cm. The patients will have to put a cross on the line at the place which corresponds best to their psychological state of the past week. 0 indicates no distress and 10 very important distress.
Time Frame
3 years
Title
Change from baseline psychological vulnerability during breast cancer treatment
Description
Psychological vulnerability assessed using BDI-II questionnaire
Time Frame
3 years
Secondary Outcome Measure Information:
Title
number of therapeutic class treatment prescribed during breast cancer treatment
Description
The therapeutic strategy is modified in case of progression: chemotherapy and/or hormonotherapy. This change in treatment can affect the quality of life and psychological vulnerability of patients. The number of therapeutic classes prescribed in this way will make it possible to describe their impact over time on patients' quality of life and psychological vulnerability.
Time Frame
3 years

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically confirmed diagnosis of invasive breast cancer (=infiltrant). NB: Mixed histologies are allowed Adult women (≥ 18 years), Positive hormonal receptors (Estrogen receptors and/or Progesterone receptors ≥10%) and HER2 negative Patient in need of a 1st metastatic treatment line NB: Patients may have received prior treatment for their cancer, but not for their metastatic disease. Performance status ≤ 1 (world health organization) Patients affiliated to a Social Security, Obtaining the patient's signed written consent Exclusion Criteria: Patient with non-metastatic breast cancer, man Negative hormonal receptors or HER2 positive Psychiatric history with specialist diagnosis Pregnant or nursing patient Patients who cannot be followed regularly for psychological reasons (cognitive problems preventing completion of questionnaires), or because of geographical remoteness. Person deprived of liberty or adult under guardianship
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
MARIO CAMPONE, MD
Organizational Affiliation
ICO NANTES
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ico Angers
City
Angers
ZIP/Postal Code
49055
Country
France
Facility Name
Ico Nantes
City
Saint Herblain
ZIP/Postal Code
44805
Country
France

12. IPD Sharing Statement

Learn more about this trial

Quality of Life and Psychological Vulnerability in Patients With RH+ Metastatic Breast Cancer

We'll reach out to this number within 24 hrs