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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04547907
Other study ID # HELEN-006
Secondary ID
Status Recruiting
Phase Phase 3
First received
Last updated
Start date September 18, 2020
Est. completion date December 31, 2024

Study information

Verified date April 2024
Source Henan Cancer Hospital
Contact Zhenzhen Liu
Phone 13603862755
Email liuzhenzhen73@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

At present, trastuzumab combined with patuzumab has become the standard neoadjuvant therapy for high-risk HER2 positive breast cancer. TCbHP has been the standard choice of neoadjuvant therapy for HER2 positive breast cancer patients with early high-risk or locally advanced HER2 positive breast cancer. Whether nab-PHP can achieve the same effect as TCbHP is still uncertain.


Description:

In order to compare the effects of nab-PHP and TCBHP chemotherapy regimens in the neoadjuvant treatment of HER2-positive breast cancer, this study randomly divided patients who met the inclusion criteria into 2 groups through a randomized control regimen. nab-PHP regimen:Albumin binding paclitaxel 125 mg / m2 (1, 8, 15 days) + trastuzumab (8 mg / kg for the first loading dose and 6 mg / kg for the sequential maintenance dose) + patuzumab (840mg for the first loading dose and 420mg for the sequential maintenance dose) ,every 21 days for 6 cycles. TCbHP regimen:Docetaxel 75 mg/m2 + carboplatin (AUC = 6) + trastuzumab(8 mg / kg for the first loading dose and 6 mg / kg for the sequential maintenance dose) + patuzumab (840mg for the first loading dose and 420mg for the sequential maintenance dose) ,every 21 days for 6 cycles. Finally, the safety and efficacy of the two chemotherapy regimens were evaluated by postoperative PCR, ORR, DFS, OS and number of adverse events.


Recruitment information / eligibility

Status Recruiting
Enrollment 688
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: 1. 18 years = age = 70 years, Performance Status- Eastern Cooperative Oncology Group (ECOG) 0-1 2. Clinical T2-T4d, or T1c with axillary LN+ 3. HER2 + invasive breast cancer confirmed by histopathology Note: HER2 expression positive refers to the tumor cells with immunohistochemical staining intensity of 3 + or confirmed positive by fluorescence in situ hybridization [fish] at least once during the pathological detection/review of primary tumor in the Department of pathology of participating research center hospital 4. Clinically measurable lesions: measurable lesions revealed by ultrasound, molybdenum target or MR (optional) within 1 month before randomization 5. Organ and bone marrow function test within one month before chemotherapy showed no chemotherapy contraindication - Absolute value of neutrophil count = 2.0×10^9 / L - Hemoglobin = 100g / L - Platelet count = 100×10^9 / L - Total bilirubin < 1.5 ULN (upper limit of normal value) - Creatinine < 1.5 × ULN - AST/ALT < 1.5×ULN 6. Echocardiography: left ventricular ejection fraction (LVEF = 55%) 7. For women of childbearing age, serum pregnancy test was negative 14 days before randomization 8. ECOG score of 0 or 1 9. Signed the informed consent form prior to patient entry Exclusion Criteria: 1. Metastatic breast cancer (Stage IV) 2. Chemotherapy, endocrine therapy, targeted therapy and reflexotherapy have been used for this disease 3. The patient had a second primary malignant tumor, except for the well treated skin cancer 4. Patients who had undergone major surgery unrelated to breast cancer within 4 weeks before enrollment, or had not recovered completely from such operations 5. Serious heart disease or discomfort, including but not limited to the following diseases: - History of heart failure or systolic dysfunction (LVEF < 50%) - high risk uncontrolled arrhythmias such as atrial tachycardia, resting heart rate > 100 BPM, significant ventricular arrhythmias (e.g., ventricular tachycardia) or higher-level atrioventricular block (i.e., mobitz II second degree atrioventricular block or third degree atrioventricular block) - angina pectoris requiring anti angina drugs - Heart valve disease with clinical significance - ECG showed transmural myocardial infarction - Poor control of hypertension (systolic blood pressure > 180 mmHg and / or diastolic blood pressure > 100 mmHg) 6. Due to serious and uncontrollable other medical diseases, the researchers believe that there are chemotherapy contraindications 7. Those who have been known to have allergic history to the drug components of this regimen; have a history of immune deficiency, including HIV positive test, or have other acquired or congenital immunodeficiency diseases, or have a history of organ transplantation;

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Albumin binding paclitaxel+ trastuzumab+ patuzumab
Albumin binding paclitaxel 125 mg / m2 (1, 8, 15 days) + trastuzumab (8 mg / kg for the first loading dose and 6 mg / kg for the sequential maintenance dose) + patuzumab (840mg for the first loading dose and 420mg for the sequential maintenance dose) ,every 21 days for 6 cycles.
Docetaxel+ carboplatin+ trastuzumab + patuzumab
Docetaxel 75 mg/m2 + carboplatin (AUC = 6) + trastuzumab(8 mg / kg for the first loading dose and 6 mg / kg for the sequential maintenance dose) + patuzumab (840mg for the first loading dose and 420mg for the sequential maintenance dose) ,every 21 days for 6 cycles.

Locations

Country Name City State
China Henan cancer hospital Zhengzhou Henan

Sponsors (1)

Lead Sponsor Collaborator
Henan Cancer Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pathological Complete Response (pCR) Percentage of Participants With Pathological Complete Response (pCR) (ypT0/is/N0M0) after 6 cycles of neoadjuvant chemotherapy through study completion, an average of 1 year
Secondary Event-free survival rate (EFS) Time from randomization to any of the following events: disease progression during neoadjuvant therapy, local or remote recurrence, second primary malignant tumor (breast cancer or other cancers) or death from any cause . 5 years after surgery
Secondary Disease-free survival (DFS) From the date of surgery to the first appearance in a local, regional, contralateral, or distant area. 5 years after surgery
Secondary number of adverse events and serious adverse events. Evaluate the nature, incidence and severity of chemotherapy adverse events according to CTCAE 4.0 After each cycle of chemotherapy (21 days as 1 cycle)
Secondary Dose adjustment rate and withdrawal rate of chemotherapy drugs Dose adjustment rate and withdrawal rate of chemotherapy drugs in two chemotherapy regimens After the end of the 6th cycle of chemotherapy (21 days as 1 cycle)
Secondary Exploratory endpoint - PCR rates for each subgroup and factors affecting pCR of the enrolled population Percentage of Participants With Pathological Complete Response (pCR) through study completion, an average of 1 year