Evaluating the Efficacy and Safety of Pyrotinib After Adjuvant Anti-HRE2 Therapy in Women With High-risk in Early or Locally Advanced Stage Breast Cancer

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

ExteNET study explored neratinib prolong anti-HER2 therapy after trastuzumab therapy found that it can improve disease-free survival in patients with lymph nodes positive; In addition, the subgroup of patients with residual tumors after neoadjuvant therapy was found to improve the survival. However, no conclusive conclusions were reached. However, since the study was carried out early so only trastuzumab treatment was used, it is urgent to carry out research that is more in line with current clinical practice and bring more benefits to patients. To explore whether pyrotinib can further reduce the risk of recurrence from previously diagnosed HER2-positive breast cancer after treatment with trastuzumab and pertuzumab or T-DM1.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
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• Subjects voluntarily participate in this study and sign the informed consent form;

• Female or male patients, aged ≥ 18 years, and ≤75 years;

• ECOG PS score: 0-1;

• Patients with HER2+ early or locally advanced breast cancer confirmed by histopathology: HER2-positive is defined by standard of 3+ by immunohistochemical staining (IHC), or 2+ by immunohistochemical staining (IHC) but positive by in situ hybridization (ISH).

• Stage II through IIIC HER-2 positive breast cancer with node positive disease after surgery.

• Been treated for early breast cancer with standard of care duration of trastuzumab combined with pertuzumab or T-DM1.

• Could have been treated neoadjuvantly but have not reached pathologic complete response.

Locations
Other Locations
China
JiangSu Province Hospital/ The First Affiliated Hospital of Nanjing Medical University
RECRUITING
Nanjing
Contact Information
Primary
Xiaoan Liu, Professor
liuxiaoan@126.com
025-68308162
Time Frame
Start Date: 2023-04-08
Estimated Completion Date: 2028-12-31
Participants
Target number of participants: 188
Treatments
Experimental: Pyrotinib
pyrotinib 400mg orally daily for one year
Related Therapeutic Areas
Sponsors
Collaborators: Jiangsu HengRui Medicine Co., Ltd.
Leads: The First Affiliated Hospital with Nanjing Medical University

This content was sourced from clinicaltrials.gov