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Real world study of trastuzumab(Zercepac) in the treatment of HER2 positive breast cancer

Real world study of trastuzumab(Zercepac) in the treatment of HER2 positive breast cancer

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100046223
Enrollment
Unknown
Registered
2021-05-11
Start date
2021-05-06
Completion date
Unknown
Last updated
2021-12-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

breast cancer

Interventions

Experimental Group:trastuzumab(Zercepac)

Sponsors

The First Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Female or male patients aged 18 and above; 2. HER2 positive (IHC 3+ and / or FISH+); 3. Patients who agree to voluntarily receive trastuzumab alone/in combination with other adjuvant therapies; 4. ECOG score is 0-1; 5. There is no serious heart, liver and kidney disease, liver and kidney function is normal in the past three weeks, CBC is normal, ECG is basically normal, and LVEF >= 50%; 6. Patients who agreed to participate in the study and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Pregnant woman or suckling period woman; 2. Expected survival is less than or equal to 3 months; 3. Mental illness or other conditions affecting patient compliance; 4. Congestive heart failure, or unstable angina pectoris, history of myocardial infarction within 6 months prior to study enrollment, uncontrolled hypertension considered by researchers, and high-risk, uncontrolled arrhythmias; 5. Uncontrolled acute infection; 6. Patients with allergic constitution and known/suspected allergy to any study drug; 7. Patients who participated in other intervention studies within 8 weeks; 8. The researchers consider that it is not suitable to participate in this experiment.

Design outcomes

Primary

MeasureTime frame
Progression-free survival;Disease-free survival;Complete pathologic remission rate;

Countries

China

Contacts

Public ContactPan Meifang

First Affiliated Hospital of Guangxi Medical University

57787677@qq.com+86 18577859909

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026