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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03047889
Other study ID # CH-BC-045
Secondary ID
Status Recruiting
Phase N/A
First received November 29, 2016
Last updated February 7, 2017
Start date April 2016
Est. completion date December 2017

Study information

Verified date February 2017
Source Chinese Academy of Medical Sciences
Contact Binghe Xu
Email syhiir@126.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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


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


Recruitment information / eligibility

Status Recruiting
Enrollment 4200
Est. completion date December 2017
Est. primary completion date April 2017
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 99 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
standard therapy
standard therapy for advanced/metastatic breast cancer

Locations

Country Name City State
China The 307th Hospital of Military Medical Sciences Beijing
China Sichuan Cancer Hospital and Institute Chengdu
China The First Affliated Hospital of Chongqing Medical University Chongqing
China FuZhou General Hospital of National Miltary Command Fuzhou
China Sun Yat-Sen University Cancer Center Guangzhou
China Harbin Medical University Cancer Hospital Harbin
China Henan Cancer Hospital Henan
China Hunan Cancer Hospital Hunan
China Jiangsu Provinces hospital Jiangsu
China Tumor Hospital of Yunnan Province Kunming
China Liaoning Cancer Hospital, Zhejiang Cancer Hospital Liaoning
China General Hospital of NingXia Medical University Ningxia
China Fudan University Shanghai Cancer Center Shanghai
China The First Hospital of China Medical University Shenyang
China Tianjin Medical University Cancer Institute & Hospital Tianjin
China Wuhan Union Hospital Wuhan
China The First Hospital of Xi'an Jiaotong University Xi'an
China Xinjiang Medical University Cancer Hospital Xinjiang
China FuJian Provincial Cancer Hospital Zhengzhou

Sponsors (1)

Lead Sponsor Collaborator
Chinese Academy of Medical Sciences

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Survival status at 3 years percentage of patients still alive at 3 years 3 years
Secondary PFS Progression-free survival of first line therapy 3 years
Secondary Survival status at 5 years percentage of patients still alive at 5 years 3 years
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