RecruitingNCT05263570
The Efficiency for Stage II-III HR+/HER2+ Early Breast Cancer Patient With Standard Neoadjuvant Therapy in Real World.
The Efficiency for Patient With Stage II-III HR+/HER2+ Early Breast Cancer With Standard Neoadjuvant Therapy: a Retrospective, Multicenter Study in Real World Settings.
Sponsor
Shengjing Hospital
Enrollment
200 participants
Start Date
Aug 1, 2022
Study Type
OBSERVATIONAL
Conditions
Summary
To observe the efficiency for patient with stage II-III HR+/HER2+ early breast cancer with standard neoadjuvant therapy, a retrospective, multicenter study in real world settings.
Eligibility
Sex: FEMALEMin Age: 18 Years
Inclusion Criteria6
- Age ≥18 years or older
- HR+/HER2- breast cancer diagnosis based on local standards
- Women having stage II-III breast cancer diagnosed based on AJCC cancer staging system (8th edition) who will be admitted because of breast cancer for the first time
- Standard Therapy, determined at the discretion of the investigator, including (TCbHP/THP/EC-THP/AC-THP)
- Complete medical history was available
- Karnofsky Performance Status (KPS) Scale score ≥ 70
Exclusion Criteria4
- Women who have received any form of anti-tumor treatment - (chemotherapy, radiotherapy, molecular targeted therapy, or endocrine therapy)
- Pregnant or breast-feeding women
- Those who have bilateral breast cancer, inflammatory breast cancer or occult breast cancer
- Those who have stage IV breast cancer
Interventions
DRUGStandard Therapy
Standard Therapy, including TCbHP, THP, EC-THP, AC-THP
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT05263570
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