Skip to content

Predictive Value of Tumor Vascular Normalization Scoring in HER-2 Positive Breast Cancer

Predictive Value of Tumor Vascular Normalization Scoring in the Response to Neoadjuvant Therapy in HER-2 Positive Breast Cancer: an Observational Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06868758
Enrollment
50
Registered
2025-03-11
Start date
2025-01-01
Completion date
2026-06-30
Last updated
2025-03-11

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

Conditions

HER2 Positive Breast Carcinoma, Neoadjuvant Therapy

Keywords

Tumor vascular normalization score, anti-HER2 antibody, Treatment efficacy

Brief summary

This study aims to evaluate the predictive value of the tumor vascular normalization score for the efficacy of neoadjuvant therapy in HER-2-positive breast cancer and explore its potential as a predictive biomarker. Through longitudinal observation of HER-2-positive breast cancer patients receiving standard treatment, we will analyze the correlation between vascular normalization scores and treatment responses (including objective response rate \[ORR\] and pathological complete response \[pCR\]) to optimize individualized therapeutic strategies. Additionally, an exploratory investigation will assess the impact of ginsenoside-containing formulations (e.g., Jinxing Capsule, Shenyi Capsule, Yiqi Jianpi Oral Liquid) on tumor vasculature and neoadjuvant therapy outcomes in HER-2-positive breast cancer, providing scientific insights for complementary therapeutic interventions.

Interventions

None listed

Sponsors

Chongqing General Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Female breast cancer patients aged ≥18 years planned for neoadjuvant therapy. * Histopathologically confirmed HER2-positive status (IHC 3+ or IHC 2+ with positive FISH confirmation). * Mentally competent, no psychiatric disorders, with good compliance to treatment and follow-up. * Voluntarily participate and provide written informed consent.

Exclusion criteria

* HER2-negative breast cancer. * Pregnant, planning pregnancy, or lactating women. * History of allergic predisposition or known/suspected allergy to study drugs. * Participation in other clinical trials within the past 4 weeks or planned enrollment. * Other conditions deemed ineligible by the investigator.

Design outcomes

Primary

MeasureTime frameDescription
Correlation between VNS and Therapeutic OutcomesPatients will be assessed at the third week and fifth week after initiation of anti-HER2 therapy, as well as preoperatively (prior to surgery).Predictive value of VNI for pCR (ROC curve analysis). Unit of Measure: Statistical correlation coefficients (R²/AUC)

Secondary

MeasureTime frameDescription
Correlation between Ginsenoside Formulation Exposure and Tumor Vascular NormalizationPatients will be assessed at the third week and fifth week after initiation of anti-HER2 therapy, as well as preoperatively (prior to surgery).Ginsenoside Exposure Measurement: Tool: Plasma concentration via Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry (UPLC-MS/MS) Parameter: Total ginsenoside plasma concentration (unit: ng/mL) Time Frame: Pre-dose and at Cycle 3 Day 1 (C3D1) of neoadjuvant therapy Vascular Normalization Measurement: Tool: Dynamic Contrast-Enhanced MRI (DCE-MRI) with Extended Tofts Model Parameter: Vascular Normalization Index (VNI) Components: K\<sup\>trans\</sup\> (unit: min\<sup\>-1\</sup\>) Plasma volume fraction (v\<sub\>p\</sub\>, unit: %) Calculation: Composite score (range 0-1) derived from principal component analysis Statistical Correlation: Method: Spearman's rank correlation Unit: Spearman's ρ (range: -1 to 1)

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026