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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05834686
Other study ID # Breast-CTC-HER2
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2023
Est. completion date April 2025

Study information

Verified date April 2023
Source Beijing 302 Hospital
Contact Jinmei Zhou
Phone 01066947250
Email jinzhu2714@sina.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To evaluate the predictive and prognostic value of HER2 expression of circulating tumor cells in HER2-positive advanced breast cancer patients treated with ADC


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date April 2025
Est. primary completion date December 2024
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria: - Has pathologically documented breast cancer that: 1. Is unresectable or metastatic 2. has confirmed HER2-positive expression defined as IHC 2+/ISH+ or IHC 3+ 3. was previously treated with trastuzumab and taxane in the advanced setting or progressed within 6 months after neoadjuvant or adjuvant treatment involving a regimen including trastuzumab and taxane - Has adequate cardiac, bone marrow, renal, hepatic and blood clotting functions - Receives anti-HER2 ADC treatment - Life expectancy > 3 months - Evidence of measurable or evaluable disease (RECIST 1.1 criteria)in the 28 days before selection - ECOG =2 Exclusion Criteria: - Has uncontrolled or significant cardiovascular disease - Has history of (noninfectious) interstitial lung disease (ILD)/pneumonitis that required steroids, has current ILD/pneumonitis, or suspected ILD/pneumonitis that cannot be ruled out by imaging at screening - Has any medical history or condition that per protocol or in the opinion of the investigator is inappropriate for the study

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
HER2 expression of circulating tumor cells
Detect HER2 expression of circulating tumor cells dynamically during ADC-based treatment in HER2-positive ABC

Locations

Country Name City State
China The Fifth Medical Center of PLA General Hospital Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Beijing 302 Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Progression free survival(PFS) PFS was defined as the time from the start of treatment to either the first documented disease progression or death from any cause 3 years
Secondary Objective response rate (ORR) ORR was defined as the proportion of patients with a complete response or a partial response 2years
Secondary Overall survival(OS) OS was defined as the time from the start of treatment to death from any cause 5 years
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