The Association of Hormonal Intake and Demographic Factors With Breast Cancer Risk. An Egyptian Case-controlled Study

NewGiza University

Status: Unknown

Conditions: Observational Study

Treatments: Drug: Dydrogesterone Tablets, Norethisterone acetate, Ethinyl estradiol, Drospirenone and ethinyl estradiol

Study type: Observational

Funder types: Other

Identifiers

NCT05135013

NewGiza University Protocol 1

Details and patient eligibility

About

The aim of the current study is to investigate the association between hormonal intake, occupational and demographic factors, and the risk of breast cancer (BC) among Egyptian females.

Full description

Methodology Design. A case-controlled study.

Setting. Breast cancer clinic and breast cancer screening unit at clinical oncology department, Ain Shams University hospital

Participants.

All cases who will be screened from the BC clinic and the BC screening unit will be assessed for eligibility according to the following inclusion & exclusion criteria:

Inclusion criteria

Age > 18 and < 70

Exclusion criteria

• Diagnosed with other concurrent malignancies.
• A prior history of another cancer.

Eligible candidates will be stratified as cases or matched controls as follows:

1. Cases (100) are those eligible patients who were diagnosed with histopathologically confirmed breast cancer and were during the past 2 years to 2021 (2019-2020).
2. Matched controls (100) are those participants presenting to the screening clinic and were not diagnosed with breast cancer during the past 2 years to 2021 (2019-2020). Candidates are to be of same range of age (+/-3 years); and similar visiting period (+/-2 months). All controls were confirmed as having no diagnosis of breast cancer, with negative findings on physical breast examination, and breast sono-mammographic screening.

Ethical consideration. The protocol will be approved by the ethical committee of NGU and the Clinical Oncology department ASU. The study will be registered at clinicaltrials.gov

Methods.

Data collection for both groups will be done through reviewing of the participants' medical records retrospectively Data collection will include the following data:

• Demographic data: name, age, sex, residence

• Anthropometric data: height, weight, waist & hip circumference & waist to hip ratio and BMI calculation

• Female & menopausal status, age at menarche

• Medical history & comorbidity (CVS, DM 1 or 2, HTN)

• Family history of other cancers, diabetes

• Occupational history

• Social history: smoking, recreational drug use, marital status, nulliparity/multi-parity and lactation

• Dietary habits and diet composition

• Lifestyle habits and degree of regular activity (sedentary, active, etc.)

• History of hormonal use as follows:

  1. Reason for hormonal use: contraception, fertility promotion, PCOS
  2. Duration of hormonal use
  3. Type of hormonal drug used: dose, hormone type, route of administration

• Breast cancer classification:

  1. • Type of pathology - 2- Molecular classification (ER, PR, Her2 receptors status) 3- Staging of BC.

Statistical analysis The frequency distribution of the parameters will be assessed. Parametric data will be presented as mean & standard deviation, while non parametric data will be presented as median & IQR. All data will be analyzed using the appropriate statistical test. Proportions will be presented using number & proportion and will be assessed by the Chi square.

Multiple logistic regression analysis will be used to calculate odds ratios (OR) and corresponding 95% confidence intervals (CI) for the various studied factors in relation to breast cancer occurrence & subtypes.

Moreover, the effect of the combined significant factors to the risk of breast cancer development will be evaluated.

Enrollment: 200 estimated patients

Sex: Female

Ages: 18 to 70 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Age > 18 and < 70

Exclusion criteria

• Diagnosed with other concurrent malignancies.
• A prior history of another cancer.

Trial design

200 participants in 2 patient groups

Cases

Description:

1.Cases (100) are those eligible patients who were diagnosed with histopathologically confirmed breast cancer and were during the past 2 years to 2021 (2019-2020).

Treatment:

Drug: Dydrogesterone Tablets, Norethisterone acetate, Ethinyl estradiol, Drospirenone and ethinyl estradiol

Matched Controls

Description:

2. Matched controls (100) are those participants presenting to the screening clinic and were not diagnosed with breast cancer during the past 2 years to 2021 (2019-2020). Candidates are to be of same range of age (+/-3 years); and similar visiting period (+/-2 months). All controls were confirmed as having no diagnosis of breast cancer, with negative findings on physical breast examination, and breast sono-mammographic screening.

Treatment:

Drug: Dydrogesterone Tablets, Norethisterone acetate, Ethinyl estradiol, Drospirenone and ethinyl estradiol