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Clinical Trials/NCT03543072
NCT03543072
Unknown
Not Applicable

A Prospective Observational Study About Adjuvant or Neoadjuvant Chemotherapy Related Adverse Effects in Postmenopausal Women With Breast Cancer

Sun Yat-sen University1 site in 1 country2,000 target enrollmentJune 15, 2018

Overview

Phase
Not Applicable
Intervention
Bisphosphonates
Conditions
Breast Cancer
Sponsor
Sun Yat-sen University
Enrollment
2000
Locations
1
Primary Endpoint
The rate of osteoporosis
Last Updated
7 years ago

Overview

Brief Summary

Breast cancer is one of the most common malignant tumor in women. About 69.75% of breast cancer women patients in China are over 45 years old. It is a multicenter prospective observational study. We collect the basic information, medical history, chemotherapy-related adverse reactions, and the results of blood lipid and bone density test before, during and after adjuvant or neoadjuvant chemotherapy. The purpose of the study is to investigate the risk factors for hyperlipidemia, cardiovascular disease, and osteoporosis in postmenopausal breast cancer patients before and after chemotherapy, and to assess the risk of future arteriosclerotic cardiovascular disease and osteoporotic fractures. In addition, the collected information of the subjects are analyzed to provide suggestions for the relevant prevention strategy.

Detailed Description

Breast cancer is one of the most common malignant tumor in women. About 69.75% of breast cancer women patients in China are over 45 years old. Chemotherapy is one of the important treatments for breast cancer, but it brings a series of adverse effects, especially increasing the risk of hyperlipidemia, cardiovascular disease and osteoporosis in postmenopausal women. It is a multicenter prospective observational study. The postmenopausal breast cancer women patients who are planning adjuvant or neoadjuvant chemotherapy are enrolled in the study after signing the informed consent form and passing the screening. We collect the basic information, medical history, chemotherapy-related adverse reactions, and the results of blood lipid and bone density test before, during and after chemotherapy. The purpose of the study is to investigate the risk factors for hyperlipidemia, cardiovascular disease, and osteoporosis in postmenopausal breast cancer patients before and after chemotherapy, and to assess the risk of future arteriosclerotic cardiovascular disease and osteoporotic fractures in this population.In addition, the collected information of the subjects are analyzed to provide suggestions for the relevant prevention strategy.

Registry
clinicaltrials.gov
Start Date
June 15, 2018
End Date
June 15, 2023
Last Updated
7 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Sun Yat-sen University
Responsible Party
Principal Investigator
Principal Investigator

wang shusen

Professor

Sun Yat-sen University

Eligibility Criteria

Inclusion Criteria

  • Informed consent form has been signed.
  • Breast cancer patients whose age is ≥ 18 years old and have been diagnosed by histological examination.
  • Postmenopausal women who are defined by any of the following:
  • Previous bilateral oophorectomy;
  • Age ≥ 60 years old;
  • Age \<60 years old, menopause at least 12 months, and follicle stimulating hormone \[FSH\] and estradiol levels in the postmenopausal range.
  • Plan for adjuvant or neoadjuvant chemotherapy.

Exclusion Criteria

  • Those who have already received adjuvant or neoadjuvant chemotherapy.
  • Those who have chemotherapy contraindications.
  • Those who have any mental condition that prevents the understanding of the contents of this study and can't provide the complete information required.

Arms & Interventions

exposure group

exposed to some factors

Intervention: Bisphosphonates

Outcomes

Primary Outcomes

The rate of osteoporosis

Time Frame: 5 years

According to the result of bone mineral density

Secondary Outcomes

  • The risk of osteoporotic fracture(5 years)

Study Sites (1)

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