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Experience of the Patient Treated With Trastuzumab (Herceptin ®) as Adjuvant for Breast Cancer

Experience of the Patient Treated With Trastuzumab (Herceptin ®) as Adjuvant for Breast Cancer: Fatigue and Quality of Life During and Waning of Treatment, Psychosocial Aspects (Environment, Work)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01400438
Acronym
HER-ception
Enrollment
70
Registered
2011-07-22
Start date
2011-07-31
Completion date
2015-09-30
Last updated
2016-07-21

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

Conditions

Breast Cancer

Keywords

Herceptin, Breast cancer, Quality of life, fatigue

Brief summary

Many studies have been devoted to the quality of life of patients during adjuvant chemotherapy for breast cancer by highlighting fatigue, psychological distress and impact on the immediate environment (spouse, children) during this difficult time for women. Curiously, no study to date has been submitted or published about how women with a one-year treatment extra Herceptin ® live this period in terms of quality of life, in terms of psychological impact for themselves and their families. The investigators have no more data on how often they return to work during this treatment or on the psycho-social parameters which underpin them. It therefore seemed interesting to give a spotlight on this particular period in these women HER2 + by comparing a patient population of same age receiving the same adjuvant but with no Herceptin ®.

Interventions

OTHERquestionnaires

delivery of questionnaires and self-psychological interview

Sponsors

Centre Francois Baclesse
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Masking
NONE

Eligibility

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

Inclusion criteria

* Women aged over 18 * Invasive breast carcinoma confirmed histologically * Non-metastatic cancer * Surgery of the primary tumor performed (mastectomy or lumpectomy) and associated with an audit axillary (sentinel node and / or axillary dissection) * Patient should receive their last course of adjuvant chemotherapy (3 FEC and 3 Taxotere) * Patients not receiving the third course of Taxotere because of toxicities may be included in the fifth course of chemotherapy is the second of Taxotere * For the group Herceptin ®: HER2 overexpression without contraindication to treatment administration * For the control group: no indication for Herceptin ® * Radiation therapy and / or adjuvant hormonal therapy allowed * Free and informed consent signed

Exclusion criteria

* Women under 18 or over 60 years * Histology other than adenocarcinoma * Metastatic Breast Cancer * Chemotherapy neoadjuvant * Surgery of the primary tumor unrealized * Lack of adjuvant chemotherapy with Taxotere 3 FEC and 3 * Patients with a history of malignancy within 5 years, outside of a basal cell cancer or cancer of the cervix treated and cured * Patient under guardianship or unable to give informed consent, * Pregnant or lactating * Patient unable to undergo a medical for geographical, social or psychopathological

Design outcomes

Primary

MeasureTime frameDescription
score of fatigueat 9 monthsThe main objective of this study is to evaluate the score of fatigue in patients with HER2 overexpressing breast cancer and for whom Herceptin ® treatment is prescribed, compared with a population of patients treated with the same age the same chemotherapy without Herceptin ®.

Secondary

MeasureTime frameDescription
Assess the quality of life3, 6, 9 and 12 monthsAssess the quality of life of patients treated for breast cancer with surgery followed by adjuvant chemotherapy (+/-hormonotherapy) associated with treatment with Herceptin ®, compared with patients of similar age treated with the same chemotherapy without Herceptin ®
Impact of Herceptin ® in the professional livesat 3, 6 ,9 and 12 monthsAssess the impact of Herceptin ® in the professional lives of patients, compared to patients not treated with Herceptin ®. Evaluation done by a specific questionnaire on professional lives, a scoring will be determined.
quantitative and qualitative psychological impact of Herceptin ®at 3 monthsAssess the quantitative and qualitative psychological impact of Herceptin ® in patients so treated, compared to patients not treated with Herceptin ®. Evaluation done by specific questionnaires, a scoring will be determined.
a qualitative sociological analysis among spouses of patientsat 6 monthsConduct a qualitative sociological analysis among spouses of patients treated with Herceptin ®. An interview with a sociologist will be done and characteristic sociologic of patients will be described.

Countries

France

Outcome results

None listed

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