Skip to main content
Clinical Trials/NCT03047889
NCT03047889
Unknown
Not Applicable

A Nation-wide Multicenter Clinical Epidemiologic Study of Chinese Females With Advanced Breast

Chinese Academy of Medical Sciences19 sites in 1 country4,200 target enrollmentApril 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Advanced Breast Cancer
Sponsor
Chinese Academy of Medical Sciences
Enrollment
4200
Locations
19
Primary Endpoint
Survival status at 3 years
Last Updated
9 years ago

Overview

Brief Summary

To study the epidemiological trends and characteristics for advanced breast cancer patients, to analyze these trends and report the results

Detailed Description

In this study, the investigators conducted a hospital-based retrospective clinical study, recruiting female advanced breast cancer patients from 14 tertiary hospitals at 7 classic geographic regions, to study the clinical epidemiologic characteristics of advanced breast cancer and the current standard of clinical diagnosis and treatment in order to provide references for standardized treatment therapy, and to improve the quality of life and prolong survival time. To study the epidemiological trends and characteristics for advanced BC patients, to analyze these trends and report the results. To learn about the current treatment therapy for advanced BC patients in different areas in China.To provide references for standardized treatment therapy, to improve the quality of patients' life and to prolong the survival time for the advanced BC patients.To assess the different treatment therapies for advanced BC with consideration of economic cost-effectiveness

Registry
clinicaltrials.gov
Start Date
April 2016
End Date
December 2017
Last Updated
9 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Binghe Xu

Professor

Chinese Academy of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • diagnosed as advanced breast cancer during Jan1st,2012-Dec31st,2014
  • complete with surgical pathology data, auxiliary treatment, there is a clear recurrence, transfer time, place, transfer of recurrence after treatment, and curative effect evaluation details.In any age, ethnic group cases.

Exclusion Criteria

  • no available medical record

Outcomes

Primary Outcomes

Survival status at 3 years

Time Frame: 3 years

percentage of patients still alive at 3 years

Secondary Outcomes

  • PFS(3 years)
  • Survival status at 5 years(3 years)

Study Sites (19)

Loading locations...

Similar Trials