A Multicenter, Randomized, Open, Phase III Trial of ddEC-THPvs Evaluating the Efficacy and Safety of TCHP Neoadjuvant Therapy for HER2-positive Breast Cancer
Study Details
Study Description
Brief Summary
The study is being conducted to assess the efficacy and safety of anthracycline-containing ddEC-THP intensive regimen and an anthracycline-free TCbHP neoadjuvant therapy for HER2-positive breast cancer
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 3 |
Detailed Description
A Multicenter, Randomized, Open, Phase III，The study is being conducted to assess the efficacy and safety of anthracycline-containing ddEC-THP intensive regimen and an anthracycline-free TCbHP neoadjuvant therapy for HER2-positive breast cancer,Subjects will be treated until disease progression, toxicity is intolerable, informed consent is withdrawn, and investigators determine that medication must be discontinued. Drug efficacy and safety data will be collected.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: TCbHP Experimental group (TCbHP) : Taxotere (75mg/m2) + Carboplatin (AUC=5) Trastuzumab 6mg/kg(initial dose 8mg/kg) Pertuzumab 420mg(initial dose 840mg) 1/21d times 6 cycle |
Drug: TCbHP VS ddEC-THP
The efficacy was evaluated every two cycles, and the effective patients (CR, PR, SD) were treated with surgery after 6 cycles. If treatment does not work, change the treatment plan according to the clinician's decision.
|
| Placebo Comparator: ddEC-THP Epirubicin (90mg/m2)+ cyclophosphamide (600mg/m2) 1/14d×4 cycle Taxol (80mg/m2) 1/7d x 12w Trastuzumab 6mg/kg(initial dose 8mg/kg) 1/21d ×4 cycles Pertuzumab 420mg(initial dose 840mg) 1/21d x 4 cycles |
Drug: TCbHP VS ddEC-THP
The efficacy was evaluated every two cycles, and the effective patients (CR, PR, SD) were treated with surgery after 6 cycles. If treatment does not work, change the treatment plan according to the clinician's decision.
|
Outcome Measures
Primary Outcome Measures
- pCR rate using the definition of ypT0/Tis ypN0 (i.e., no invasive residual in breast or nodes; noninvasive breast residuals allowed) at the time of definitive surgery [Up to approximately 24 weeks]
pCR rate (ypT0/is，ypN0) is defined as the percentage of participants without residual invasive tumor on hematoxylin and eosin evaluation of breast specimen and all sampled regional lymph nodes following completion of neoadjuvant systemic therapy by current AJCC staging criteria assessed by the local pathologist at the time of definitive surgery in all participants.
Secondary Outcome Measures
- Event-Free Survival (EFS) [Up to approximately 3 years]
EFS is defined as the time from start of study treatment to any of the following events: progression of disease that precludes surgery, local or distant recurrence, second primary malignancy (breast or other cancers) or death due to any cause.
- Invasive Disease-Free Survival (iDFS) [Up to approximately 3 years]
iDFS events are defined as follows: (1)Ipsilateral invasive breast tumor recurrence. (2) Ipsilateral local-regional invasive breast cancer recurrence. (3) Ipsilateral second primary invasive breast cancer. (4) Contralateral invasive breast cancer. (5) Distant recurrence. (6) Death attributable to any cause.
- Overall survival (OS) [Up to approximately 3 years]
OS is defined as the time from randomization to death due to any cause. Participants without documented death at the time of the analysis will be censored at the date of the last follow-up.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Age: 18 ~70 years old, female;
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Histologically confirmed patients with previously untreated stage Ⅱ-Ⅲ HER2-positive breast cancer;
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HER-2 positive breast cancer, defined as immunohistochemical (IHC) detection of 3+ or in situ hybridization (FISH) results of HER2 gene amplification;
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There is at least one measurable objective lesion according to RECIST 1.1 criteria;
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ECOG Physical fitness score is 0-2;
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Left ventricular ejection fraction LVEF≥50%;
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Bone marrow function: neutrophils ≥1.5×109/L, platelets ≥100×109/L, hemoglobin ≥90g/L;
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Liver and kidney function: serum creatinine ≤1.5 times the upper limit of normal value; AST and ALT≤2.5 times the upper limit of normal, or ≤5 times the upper limit of normal in the presence of liver metastasis; Total bilirubin ≤1.5 times the upper limit of normal, or ≤2.5 times the upper limit of normal in patients with Gilbert's syndrome, creatinine clearance greater than 30 mL/min;
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For female patients who are not menopausal or have not been surgically sterilized: consent to abstinence or use an effective contraceptive method during treatment and for at least 7 months after the last dose in the study treatment
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The patient has good compliance with the planned treatment, can understand the research process of the study and sign the written informed consent.
Exclusion Criteria:
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Stage IV (metastatic) breast cancer patients;
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Patients with inflammatory breast cancer
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Serious heart disease or discomfort, including but not limited to:
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History of heart failure or systolic dysfunction (LVEF < 50%)
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High-risk uncontrolled arrhythmias such as atrial tachycardia, resting heart rate
100 bpm, significant ventricular arrhythmias (e.g., ventricular tachycardia) or higher-grade atrioventricular block (i.e., Mobitz II second-degree atrioventricular block or third-degree atrioventricular block) Angina pectoris that requires antiangina medication
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valvular heart disease of clinical significance
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ECG showed transmural myocardial infarction
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Poor hypertension control (systolic blood pressure > 180 mmHg and/or diastolic blood pressure > 100 mmHg)
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Known allergic history of drug components of this protocol; A history of immunodeficiency, including HIV positive, or other acquired, congenital immunodeficiency diseases, or a history of organ transplantation;
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Patients with severe systemic infection or accompanied by other serious diseases;
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Have developed other malignant tumors within the previous 5 years, except for cured cervical carcinoma in situ and non-melanoma skin cancer;
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Pregnant and lactating women, fertile women who tested positive for baseline pregnancy tests, or patients of childbearing age who were unwilling to take effective contraceptive measures during the entire trial period and within 6 months after the last study;
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Patients who participated in other studies within 30 days prior to the first dose of the investigational drug;
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Patients deemed unsuitable for this study by the investigator.
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The patient has good compliance with the planned treatment, can understand the research process of the study and sign the written informed consent.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Breast Oncology, Tianjin Medical University Cancer Institute and Hospital | Tianjin | Tianjin | China | 300060 |
Sponsors and Collaborators
- Tianjin Medical University Cancer Institute and Hospital
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- CIH-TZS-20201008-01