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Dynamic monitoring of serum adenosine to predict the efficacy and prognosis of trastuzumab in patients with HER2-positive metastatic breast cancer

Dynamic monitoring of serum adenosine to predict the efficacy and prognosis of trastuzumab in patients with HER2-positive metastatic breast cancer

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100052290
Enrollment
Unknown
Registered
2021-10-24
Start date
2022-01-01
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Breast cancer

Interventions

Gold Standard:Clinical outcome
Index test:serum&#32

Sponsors

Jiangsu Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Female patients with metastatic breast cancer (MBC) admitted to our hospital from January 2021 to December 2023; 2. The patients aged between 18 and 70 years, and immunohistochemistry (3+) or fluorescence in situ hybridization (FISH, HER2/CEP17 ratio >= 2.0) are HER2 positive; 3. Hormone receptor status has been detected; 4. Left ventricular ejection fraction is more than 50%; 5. ECOG PS<=2; 6. The organ function of the enrolled patients is good; 7. Before enrollment, patients received endocrine therapy; 8. Patients may have received adjuvant chemotherapy or neoadjuvant chemotherapy, including or not including trastuzumab, before enrollment, with an interval of at least 6 months from the completion of adjuvant therapy or neoadjuvant therapy to the diagnosis of metastatic breast cancer; 9. Fully understand the study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Central nervous system transfer; 2. Prior exposure to a cumulative dose of doxorubicin exceeding 360 mg/m^2 or equivalent; 3. Other investigators judged that it did not conform to the situation of this study.

Design outcomes

Primary

MeasureTime frame
Overall response rate at 24 weeks;

Secondary

MeasureTime frame
Disease control rate;Duration of remission;Progression free survival;

Countries

China

Contacts

Public ContactHe Xia

Jiangsu Cancer Hospital

hexiabm@163.com+86 13601458518

Outcome results

None listed

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