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Exploration of the role of Xihuangwan in synergistic neoadjuvant treatment of triple-negative breast cancer through immunogenic mortality

Exploration of the role of Xihuangwan in synergistic neoadjuvant treatment of triple-negative breast cancer through immunogenic mortality

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000822
Enrollment
Unknown
Registered
2025-04-22
Start date
2023-01-01
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Breast cancer

Interventions

TCA group:Epirubicin + cyclophosphamide + docetaxel neoadjuvant therapy
TCA program + Xihuangwan group:Epirubicin + cyclophosphamide + docetaxel + xihuangwan neoadjuvant therapy
control subjects:No special treatment
Xihuangwan group:3 days of Xihuangwan treatment during preparation for surgery

Sponsors

The Second Affiliated Hospital of Shandong First Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) female patients with triple-negative breast cancer diagnosed by puncture histology: (2) age =18 and =75 years old not receiving neoadjuvant/adjuvant chemotherapy: (3) patients with an ECOG score of =1; (4) conscious judgmental about pain able to cooperate in evaluating pain and quality of life and with normal expressive ability; (5) voluntarily signing an informed consent form; and (6) agreeing to undergo epirubicin + cyclophosphamide + docetaxel + xihuangwan neoadjuvant therapy

Exclusion criteria

Exclusion criteria: (1) Mental disorders language disorders; (2) Combined visceral metastases; (3) Combined severe cardiac pulmonary hepatic and renal dysfunction; (4) Nursing women pregnant women; (5) Cannot sign the informed consent; (6) Incomplete information to judge the efficacy of the treatment; (7) Can not cooperate with the treatment and withdraw halfway; (8) Changes in the condition need to change the treatment.

Design outcomes

Primary

MeasureTime frame
Immunohistochemical detection of CRT HMGB1 HSP70/90;

Secondary

MeasureTime frame
Determination of tumor diameter by color ultrasound;

Countries

China

Contacts

Public ContactXingchao Xu

The Second Affiliated Hospital of Shandong First Medical University No.366 Taishan Street Tai'an City Shandong Province China

xuxingchao1@163.com+86 156 2134 7773

Outcome results

None listed

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