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An observational study to evaluate the prognostic value of inflammatory indicators such as neutrophil/lymphocyte ratio (NLR) at baseline in breast cancer

An observational study to evaluate the prognostic value of inflammatory indicators such as neutrophil/lymphocyte ratio (NLR) at baseline in breast cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400081952
Enrollment
Unknown
Registered
2024-03-18
Start date
2024-03-18
Completion date
Unknown
Last updated
2024-03-25

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

Conditions

breast cancer

Interventions

receiving HER2 targeted drugs trastuzumab + pertuzumab:None
receiving HER2 targeted drugs trastuzumab:none

Sponsors

Xiangya Hospital, Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Female patients aged 18 or older and less than or equal to 70 years old; 2. All patients were diagnosed as HER-2 positive breast cancer by histopathology; 3. The functional level of organs is basically normal: bone marrow function, liver and kidney function, heart; 4. In the late stage, they have not received chemotherapy or biotherapy for metastatic disease; 5. The Eastern Cooperative Oncology Group (ECOG) performance status is 0 or =1; 6. Left ventricular ejection fraction (LVEF) is at least 50%; 7. The first-line treatment for advanced cancer is based on paclitaxel, with or without targeted therapy.

Exclusion criteria

Exclusion criteria: 1. Those who have received any form of traditional Chinese medicine treatment in the first-line treatment in the late stage; 2. Accepting other anti-tumor treatments for other tumors at the same time; 3. Bilateral breast cancer, inflammatory breast cancer or occult breast cancer, central nervous system metastasis; 4. Having had other malignant tumors in the past 5 years, except for cured cervical carcinoma in situ; 5. Patients with severe dysfunction of important organs such as the heart, liver, and kidneys; 6. Have any previous heart disease, including: (1) arrhythmia requiring medication or having clinical significance; (2) myocardial infarction; (3) heart failure; (4) any other heart disease judged by the investigator as not suitable for participating in this trial; 7. Female patients in pregnancy and lactation period; 8. There are infectious diseases, such as chronic pneumonia in the acute phase, tuberculosis, hepatitis; Existence of autoimmune diseases, such as lupus erythematosus, chronic glomerulonephritis, etc; 9. Patients with acute and chronic injuries, blood system diseases, and end-stage renal disease.

Design outcomes

Primary

MeasureTime frame
Correlation between neutrophil/lymphocyte ratio and progression free survival (PFS) of breast cancer;

Secondary

MeasureTime frame
Correlation between platelet/lymphocyte ratio and progression free survival (PFS) of breast cancer;Correlation between systemic immune inflammation index and disease-free progression of breast cancer (PFS);

Countries

China

Contacts

Public ContactZhi Xiao

Xiangya Hospital, Central South University

zhixiao@csu.edu.cn+86 189 7513 8230

Outcome results

None listed

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