Pyrotinib in Women With High-risk in Early Stage Breast Cancer

Sponsor
The First Affiliated Hospital with Nanjing Medical University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05834764
Collaborator
Jiangsu HengRui Medicine Co., Ltd. (Industry)
188
1
1
68.8
2.7

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
Phase 2

Study Design

Study Type:
Interventional
Anticipated Enrollment :
188 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
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
Actual Study Start Date :
Apr 8, 2023
Anticipated Primary Completion Date :
Jun 1, 2026
Anticipated Study Completion Date :
Dec 31, 2028

Arms and Interventions

Arm Intervention/Treatment
Experimental: Pyrotinib

pyrotinib 400mg orally daily for one year

Drug: Pyrotinib
Pyrotinib after anti-HER2 therapy(Trastuzumab combined with Pertuzumab or T-DM1)
Other Names:
  • Pyrotinib maleate
  • Outcome Measures

    Primary Outcome Measures

    1. Invasive Disease-free Survival (iDFS) at year 2 [From enrollment until time of events up to 2 years]

      Invasive disease-free survival time is defined as the time from date of enrollment until the first disease recurrence or death from any cause.

    Secondary Outcome Measures

    1. Disease-free Survival at year 2 (2y-DFS) [From enrollment until time of events up to 2 years]

      Disease-free survival time is defined as the time from date of enrollment until the first disease recurrence(including carcinoma in situ)or death from any cause.

    2. Overall Survival (OS) [Enrollment until death due to any cause, up to 10 years]

      Randomization to death from any cause

    3. Invasive Disease-free Survival (iDFS) at year 5 [From enrollment until time of events up to 5 years]

      Invasive disease-free survival time is defined as the time from date of enrollment until the first disease recurrence or death from any cause.

    4. AEs and SAEs [From the first administration to one months after the last drug administration]

      Adverse events and Adverse events and serious adverse events according to CACTE 5.0

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 75 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Subjects voluntarily participate in this study and sign the informed consent form;

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

    3. ECOG PS score: 0-1;

    4. 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).

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

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

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

    Exclusion Criteria:
    1. metastatic disease (Stage IV) or inflammatory breast cancer

    2. Previous or current history of malignant neoplasms, except for curatively treated:Basal and squamous cell carcinoma of the skin,Carcinoma in situ of the cervix.

    3. Clinically relevant cardiovascular disease:Known history of uncontrolled or symptomatic angina, clinically significant arrhythmias, congestive heart failure, transmural myocardial infarction, uncontrolled hypertension ≥180/110);

    4. A history of allergy to the drugs in this study;

    5. Unable or unwilling to swallow tablets

    6. History of gastrointestinal disease with diarrhea as the major symptom.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 JiangSu Province Hospital/ The First Affiliated Hospital of Nanjing Medical University Nanjing Jiangsu China

    Sponsors and Collaborators

    • The First Affiliated Hospital with Nanjing Medical University
    • Jiangsu HengRui Medicine Co., Ltd.

    Investigators

    • Principal Investigator: Xiaoan Liu, Professor, Jiangsu Province Hospital/ The First Affiliated Hospital of Nanjing Medical University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Liu Xiaoan, Professor, The First Affiliated Hospital with Nanjing Medical University
    ClinicalTrials.gov Identifier:
    NCT05834764
    Other Study ID Numbers:
    • OBU-BC-II-083
    First Posted:
    Apr 28, 2023
    Last Update Posted:
    Apr 28, 2023
    Last Verified:
    Apr 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 28, 2023