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A multi-center, observational study to describe the treatment situation of Chinese County Population with HER2+ & HR+/HER2- Breast Cancer

A multi-center, observational study to describe the treatment situation of Chinese County Population with HER2+ & HR+/HER2- Breast Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200063764
Enrollment
Unknown
Registered
2022-09-16
Start date
2022-09-15
Completion date
Unknown
Last updated
2023-04-17

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

Conditions

breast cancer

Interventions

None listed

Sponsors

The First Affiliated Hospital of Xinxiang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Cohort 1 Aged >= 18 years at the time of enrollment; Histologically confirmed HER2+ breast cancer; Newly diagnosed or completed definitive early breast surgery; Complete medical history information. Cohort 2 Age >= 18 years at the time of enrollment; Histologically confirmed HR+ HER2- breast cancer; Newly diagnosed or completed definitive early breast surgery; Complete medical history information. Cohort 3 Age >= 18 years at the time of enrollment; Histologically confirmed HER2+ breast cancer; De Novo or recurrent metastatic breast cancer; Complete medical history information. Cohort 4 Age >= 18 years at the time of enrollment; Histologically confirmed HR+ HER2- breast cancer; De Novo or recurrent metastatic breast cancer; Complete medical history information.

Exclusion criteria

Exclusion criteria: Cohort 1 Participated in other Intervention drug clinical trials within 4 weeks before admission. Cohort 2 Participated in other Intervention drug clinical trials within 4 weeks before admission. Cohort 3 Patients with HER2 + advanced breast cancer who have received more than 2 lines of therapy; Participated in other Intervention drug clinical trials within 4 weeks before admission. Cohort 4 Patients with HR+ HER2- advanced breast cancer who have received more than 2 line of therapy; Participated in other Intervention drug clinical trials within 4 weeks before admission.

Design outcomes

Primary

MeasureTime frame
To describe the treatment pattern on HER2+ & HR+HER2- early and advanced breast cancer in county;

Secondary

MeasureTime frame
To describe the referral behavior in county (Among all patients);To explore the relationship between recurrent risk and OFS, chemotherapy and OFS;To explore the duration of medical OFS in early breast cancer;To explore the duration of anti-HER2 therapy in advanced breast cancer;

Countries

China

Contacts

Public ContactPing Lu

The First Affiliated Hospital of Xinxiang Medical College

lupingdoctor@126.com+86 13598722864

Outcome results

None listed

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