Breast Cancer Clinical Trial
Official title:
The French E3N Prospective Cohort Study (Etude Epidémiologique auprès de Femmes de la Mutuelle Générale de l'Education Nationale)
The French E3N cohort was initiated in 1990 to investigate the risk factors associated with
cancer and other major non-communicable diseases in women.
The participants were insured through a national health system that primarily covered
teachers, and were enrolled from 1990 after returning baseline self-administered
questionnaires and providing informed consent. The cohort comprised nearly 100 000 women with
baseline ages ranging from 40 to 65 years.
Follow-up questionnaires were sent approximately every 2-3 years after the baseline and
addressed general and lifestyle characteristics together with medical events (cancer,
cardiovascular diseases, diabetes, depression, fractures and asthma, among others). The
follow-up questionnaire response rate remained stable at approximately 80%.
A biological material bank was generated and included blood samples collected from 25 000
women and saliva samples from an additional 47 000 women.
Ageing among the E3N cohort provided the opportunity to investigate factors related to
agerelated diseases and conditions as well as disease survival.
Who is in the cohort? In June 1990, a questionnaire was sent to 500 000 women who had been
born between 1925 and 1950 and were insured by the Mutuelle Générale de l'Education Nationale
(MGEN), a national health insurance plan that primarily covers teachers. The questionnaire
was sent along with a leaflet explaining that an Inserm research team was launching a study
of cancer risk factors and that participation would require filling in questionnaires every
2-3 years as well as the submission of a signed consent form providing permission to obtain
information about each participant's vital status, address changes and medical expense
reimbursements from the insurance plan. Nearly 100 000 women volunteered.
How often have they been followed-up? Until now, nine follow-up questionnaires have been sent
every 2-3 years from the baseline. Approximately half of the answers were obtained after the
first mailing. Two reminders were sent thereafter. The questionnaires were accompanied with
newsletters that informed participants about the major results obtained to date. The
participation rate remained high (77-92% according to the questionnaires) and the lost to
follow-up rate was minimal because of the ability to trace non-respondents through their
insurance plan files. The questionnaires were accurately filled in, with few missing or
unacceptable answers.
What has been measured? To date, 11 self-administered questionnaires have been sent. The
collected data are sociodemographic factors, anthropometric measurements, reproductive
factors, hormonal treatments, health behaviour and lifestyle. Each follow-up questionnaire
also recorded the participant's health status. The questionnaires are available at www.e3n.fr
.
The questionnaires are anonymous and identified with an identification number and pin code
that can be rapidly scanned to identify the respondents. The questionnaires are optically
scanned and all answers are checked on screen. The scanned images are saved to allow data
entry at a later time, including information regarding the addresses of medical doctors (18
000 to date) or drug names (pre-listed to avoid errors). The longitudinal data (repeats of
identical questions for the purpose of updating information about topics such as menopause or
smoking) are routinely homogenized. Several validation studies (e.g. dietary and
anthropometrical data studies) have been performed and have revealed very satisfactory
results.
Self-reported cases of cancer are validated and coded after reviewing the pathology reports
obtained from medical practitioners, and nearly 90% of all cancer cases are histologically
confirmed. Other diseases are also validated (e.g. diabetes, myocardial infarction, stroke,
Parkinson disease) by requesting additional information about the participants (e.g.
glycosylated haemoglobin levels, fracture-related circumstances, drug names) and sending
questionnaires to medical doctors.
Additionally, a biological material bank was generated. Blood samples were initially
collected from 1994-99. The participation rate among the invited participants was
approximately 40%; this yielded approximately 25 000 blood samples that were each separated
into 28 aliquots (e.g. plasma, serum, leukocytes, erythrocytes). Plastic straws were used to
store each participant's samples in liquid nitrogen containers. The bio-repositories are
located at the IARC (Lyon) and the EFS (Etablissement Français du Sang, Annemasse). Since
2004, approximately 10 case-control studies have been conducted (approximately 1 800 cases
and 3 500 controls) with regard to the measurements of various biomarkers (e.g. fatty acids,
calcium, vitamin D, vitamin B, cholesterol and C-reactive protein). A metabolomics study is
currently ongoing.
From 2009-11, saliva samples (Oragene, DNA Genotek, Kanata, ON, Canada) were requested from
68 242 living women and were obtained from 47 000 women (participation rate, 69%). Salivary
DNA has been extracted and has been used for genotyping in two case-control studies
(approximately 2 500 cases and 850 controls) since December 2010.
The research team is currently planning to set up a tumour tissue bank and will begin with
the collection of breast cancer tissues.
What has it found? The E3N cohort has produced a spectrum of results regarding the complex
roles played by nutrition, hormonal factors, physical activity, anthropometric
characteristics and other major lifestyle-related factors with respect to various diseases.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT04681911 -
Inetetamab Combined With Pyrotinib and Chemotherapy in the Treatment of HER2 Positive Metastatic Breast Cancer
|
Phase 2 | |
Terminated |
NCT04066790 -
Pyrotinib or Trastuzumab Plus Nab-paclitaxel as Neoadjuvant Therapy in HER2-positive Breast Cancer
|
Phase 2 | |
Completed |
NCT04890327 -
Web-based Family History Tool
|
N/A | |
Completed |
NCT03591848 -
Pilot Study of a Web-based Decision Aid for Young Women With Breast Cancer, During the Proposal for Preservation of Fertility
|
N/A | |
Recruiting |
NCT03954197 -
Evaluation of Priming Before in Vitro Maturation for Fertility Preservation in Breast Cancer Patients
|
N/A | |
Terminated |
NCT02202746 -
A Study to Assess the Safety and Efficacy of the VEGFR-FGFR-PDGFR Inhibitor, Lucitanib, Given to Patients With Metastatic Breast Cancer
|
Phase 2 | |
Active, not recruiting |
NCT01472094 -
The Hurria Older PatiEnts (HOPE) With Breast Cancer Study
|
||
Completed |
NCT06049446 -
Combining CEM and Magnetic Seed Localization of Non-Palpable Breast Tumors
|
||
Withdrawn |
NCT06057636 -
Hypnosis for Pain in Black Women With Advanced Breast Cancer: A Feasibility Study
|
N/A | |
Recruiting |
NCT05560334 -
A Single-Arm, Open, Exploratory Clinical Study of Pemigatinib in the Treatment of HER2-negative Advanced Breast Cancer Patients With FGFR Alterations
|
Phase 2 | |
Active, not recruiting |
NCT05501769 -
ARV-471 in Combination With Everolimus for the Treatment of Advanced or Metastatic ER+, HER2- Breast Cancer
|
Phase 1 | |
Recruiting |
NCT04631835 -
Phase I Study of the HS-10352 in Patients With Advanced Breast Cancer
|
Phase 1 | |
Completed |
NCT04307407 -
Exercise in Breast Cancer Survivors
|
N/A | |
Recruiting |
NCT03544762 -
Correlation of 16α-[18F]Fluoro-17β-estradiol PET Imaging With ESR1 Mutation
|
Phase 3 | |
Terminated |
NCT02482389 -
Study of Preoperative Boost Radiotherapy
|
N/A | |
Enrolling by invitation |
NCT00068003 -
Harvesting Cells for Experimental Cancer Treatments
|
||
Completed |
NCT00226967 -
Stress, Diurnal Cortisol, and Breast Cancer Survival
|
||
Recruiting |
NCT06019325 -
Rhomboid Intercostal Plane Block on Chronic Pain Incidence and Acute Pain Scores After Mastectomy
|
N/A | |
Recruiting |
NCT06037954 -
A Study of Mental Health Care in People With Cancer
|
N/A | |
Recruiting |
NCT06006390 -
CEA Targeting Chimeric Antigen Receptor T Lymphocytes (CAR-T) in the Treatment of CEA Positive Advanced Solid Tumors
|
Phase 1/Phase 2 |