Clinical trial · Interventional
Pyrotinib Rechallenge in Her2-positive Metastatic Breast Cancer Pretreated With Pyrotinib and Trastuzumab
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Pyrotinib is an oral tyrosine kinase inhibitor targeting both HER-1 and HER-2 receptors. This study is a randomized, open-label, multi-center, parallel design study of the combination of pyrotinib, trastuzumab and chemotherapy versus trastuzumab and chemotherapy in HER2+ MBC patients, who have prior received trastuzumab and pyrotinib. Patients will be randomized in a 2:1 ratio to one of the following treatment arms. Arm A: pyrotinib + trastuzumab + chemotherapy, Arm B: trastuzumab + chemotherapy. Patients will receive either arm of therapy until disease progression, unacceptable toxicity, or withdrawal of consent.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| HER2-positive Breast Cancer | HER2-Positive Breast Carcinoma | ALIAS | 0.90 |
| Metastatic Breast Cancer | Malignant Breast Neoplasm | CURATED_BROADER | 0.78 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Trastuzumab in combination with pyrotinib plus chemotherapy | Drug | — | UNRESOLVED |
| Trastuzumab plus chemotherapy | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Trastuzumab plus chemotherapy
- interventionNames
- Drug: Trastuzumab plus chemotherapy
- type
- EXPERIMENTAL
- label
- Pyrotinib in combination with Trastuzumab plus chemotherapy
- interventionNames
- Drug: Trastuzumab in combination with pyrotinib plus chemotherapy
Primary outcomes (1)
- measure
- Progression Free Survival (PFS)
- timeFrame
- approximately 8 months
Secondary outcomes (2)
- measure
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. Aged ≥18 and ≤75 years; 2. Pathologically confirmed HER2 positive patients with recurrence/ metastatic breast cancer: HER2 IHC 3+, or HER2 IHC 2+ and FISH detection gene amplification; 3. History of trastuzumab-containing chemotherapy in neoadjuvant, adjuvant or recurrence/ metastatic setting; 4. History of pyrotinib-containing chemotherapy in neoadjuvant or recurrence/ metastatic setting; 5. Previously reveived ≤2 systemic treatment in recurrence/ metastasis setting; (anti-HER2 ADCs such as T-DM1 is included in chemotherapy regimens, endocrine therapy alone is not included); 6. ECOG performance status of 0 to 1; 7. According to RECIST 1.1, at least one extracranial measurable lesion exists; 8. Signed informed consent. Exclusion Criteria: 1. Patients with leptomeningeal metastasis or unstable brain metastasis; 2. History of neurological or psychiatric disorders; 3. Second malignancies within 5 years, except for cured skin basal cell carcinoma, carcinoma in-situ of uterine cervix and squamous-cell carcinoma; 4. Undergone major surgical procedures or significant trauma within 4 weeks prior to randomization, or expected to undergo major surgery. 5. Factors influencing the usage of oral administration (e.g. unable to swallow, chronic diarrhea and intestinal obstruction, etc.); 6. History of allergies to the drug components of this regimen; 7. History of Immunodeficiency, acquired or congenital immunodeficiency (HIV positive), history of organ transplantation; 8. Any other situations judged by investigator as not suitable for participating in this study.
References
Publications (1)
- DERIVEDDai L, Gao T, Guo R, Chen Y, Wang J, Zhou S, Tang Y, Chen D, Huang S. Efficacy and safety of pyrotinib-based regimens in HER2 positive metastatic breast cancer: A retrospective real-world data study. Neoplasia. 2024 Oct;56:101029. doi: 10.1016/j.neo.2024.101029. Epub 2024 Jul 17. PMID 39024777