Study Comparing EC-T Verses PCb in the Adjuvant Chemotherapy of Non-triple Negative Breast Cancer

NCT ID: NCT04193059

Last Updated: 2025-11-26

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE3
• Total Enrollment: 1560 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-12-20
• Study Completion Date: 2027-07-31

Brief Summary

This study is a randomized, single center, phase III clinical trial comparing the efficacy and safety of four cycles of epirubicin combined with cyclophosphamide followed by four cycles of docetaxel (EC*4-T*4) verses 6 cycles of weekly paclitaxel combined with carboplatin (PCb*6) in the adjuvant chemotherapy of non-triple negative breast cancer patients. The study is divided in to 2 branches: PANSY-1 and PANSY-2. PANSY-1 is a study of hormone receptor (HR)-positive/human epidermal growth factor receptor-2 (HER2)-negative patients with ≥4 positive lymph node, while PANSY-2 is a study of HER2-positive patients with ≥1 positive lymph node.

Detailed Description

PANSY-1 will be comparing the efficacy and safety of four cycles of epirubicin combined with cyclophosphamide followed by four cycles of docetaxel (EC-T) verses six cycles of paclitaxel combined with carboplatin (PCb).

PANSY-2 will be comparing the efficacy and safety of four cycles of epirubicin combined with cyclophosphamide followed by four cycles of docetaxel with trastuzumab (EC-TH) verses six cycles of paclitaxel combined with carboplatin and trastuzumab (PCbH); both followed by 1 year adjuvant trastuzumab.

After pertuzumab became legally available in China, participants of PANSY-2 may choose to receive trastuzumab and pertuzumab dual targeted therapy, thus comparing the efficacy and safety of four cycles of epirubicin combined with cyclophosphamide followed by four cycles of docetaxel with trastuzumab and pertuzumab (EC-THP) verses six cycles of paclitaxel combined with carboplatin, trastuzumab and pertuzumab (PCbHP); both followed by 1 year adjuvant trastuzumab and pertuzumab.

With the inclusion of pertuzumab in China's medical insurance in January 2020, study protocols were revised to include dual targeted therapy for HER2-positive participants.

Conditions

Breast Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

PANSY-1: EC-T

4 cycles of EC (epirubicin 90 mg/m\^2 ivgtt d1+ cyclophosphamide 600 mg/m\^2 iv d1, 21 days per cycle), followed by 4 cycles of T (docetaxel 100 mg/m\^2 ivgtt d1, 21 days per cycle)

Group Type: ACTIVE_COMPARATOR

Epirubicin

Intervention Type: DRUG

epirubicin 90 mg/m\^2 ivgtt d1, 21 days per cycle, 4 cycles.

Cyclophosphamide

Intervention Type: DRUG

cyclophosphamide 600 mg/m\^2 iv d1, 21 days per cycle, 4 cycles.

Docetaxel

Intervention Type: DRUG

docetaxel 100 mg/m\^2 ivgtt d1, 21 days per cycle, 4 cycles.

PANSY-1: PCb

6 cycles of weekly PCb (paclitaxel 80 mg/m\^2 ivgtt d1, d8, d15+ carboplatin Area Under Curve (AUC)=2 ivgtt d1, d8, d15, 28 days per cycle)

Group Type: EXPERIMENTAL

Paclitaxel

Intervention Type: DRUG

paclitaxel 80 mg/m\^2 ivgtt d1, d8, d15, 28 days per cycle, 6 cycles.

Carboplatin

Intervention Type: DRUG

carboplatin AUC=2 ivgtt d1, d8, d15, 28 days per cycle, 6 cycles.

PANSY-2: EC-TH(P)

4 cycles of EC (epirubicin 90 mg/m\^2 ivgtt d1+cyclophosphamide 600 mg/m\^2 iv d1, 21 days per cycle), followed by 4 cycles of TH(P) (docetaxel 100 mg/m\^2 ivgtt d1 + trastuzumab 6 mg/kg (loading dose 8mg/kg) ivgtt d1, 21 days per cycle, with pertuzumab 420mg (loading dose 840mg) ivgtt d1, 21 days per cycle for participants receiving dual-targeted therapy). After 8 cycles of chemotherapy, patient will continue to complete 1 year of adjuvant trastuzumab (6 mg/kg ivgtt every 3 weeks), with pertuzumab (420mg ivgtt every 3 weeks) for participants receiving dual-targeted therapy.

Group Type: ACTIVE_COMPARATOR

Epirubicin

Intervention Type: DRUG

epirubicin 90 mg/m\^2 ivgtt d1, 21 days per cycle, 4 cycles.

Cyclophosphamide

Intervention Type: DRUG

cyclophosphamide 600 mg/m\^2 iv d1, 21 days per cycle, 4 cycles.

Trastuzumab

Intervention Type: DRUG

trastuzumab 6 mg/kg (loading dose 8mg/kg) ivgtt d1, 21 days per cycle with chemotherapy; or trastuzumab 2 mg/kg (loading dose 4mg/kg, w1) ivgtt d1, d8, d15, d22, 28 days per cycle with chemotherapy. After chemotherapy, patient will continue to complete 1 year of adjuvant trastuzumab (6 mg/kg ivgtt every 3 weeks).

Pertuzumab

Intervention Type: DRUG

pertuzumab 420mg (loading dose 840mg) ivgtt d1, 21 days per cycle with chemotherapy. After chemotherapy, patient will continue to complete 1 year of adjuvant pertuzumab (420mg ivgtt every 3 weeks).

Docetaxel

Intervention Type: DRUG

docetaxel 100 mg/m\^2 ivgtt d1, 21 days per cycle, 4 cycles.

PANSY-2: PCbH(P)

6 cycles of weekly PCbH(P) (paclitaxel 80 mg/m\^2 ivgtt d1, d8, d15 + carboplatin AUC=2 ivgtt d1, d8, d15 + trastuzumab 2 mg/kg (loading dose 4mg/kg, w1) ivgtt d1, d8, d15, d22, 28 days per cycle, with pertuzumab 420mg (loading dose 840mg) ivgtt d1, 21 days per cycle for participants receiving dual-targeted therapy). Participants may also choose to receive trastuzumab 6 mg/kg (loading dose 8mg/kg) ivgtt d1, 21 days per cycle with chemotherapy. After 6 cycles of chemotherapy, patient will continue to complete 1 year of adjuvant trastuzumab (6 mg/kg ivgtt every 3 weeks), with pertuzumab (420mg ivgtt every 3 weeks) for participants receiving dual-targeted therapy.

Group Type: EXPERIMENTAL

Paclitaxel

Intervention Type: DRUG

paclitaxel 80 mg/m\^2 ivgtt d1, d8, d15, 28 days per cycle, 6 cycles.

Carboplatin

Intervention Type: DRUG

carboplatin AUC=2 ivgtt d1, d8, d15, 28 days per cycle, 6 cycles.

Trastuzumab

Intervention Type: DRUG

trastuzumab 6 mg/kg (loading dose 8mg/kg) ivgtt d1, 21 days per cycle with chemotherapy; or trastuzumab 2 mg/kg (loading dose 4mg/kg, w1) ivgtt d1, d8, d15, d22, 28 days per cycle with chemotherapy. After chemotherapy, patient will continue to complete 1 year of adjuvant trastuzumab (6 mg/kg ivgtt every 3 weeks).

Pertuzumab

Intervention Type: DRUG

pertuzumab 420mg (loading dose 840mg) ivgtt d1, 21 days per cycle with chemotherapy. After chemotherapy, patient will continue to complete 1 year of adjuvant pertuzumab (420mg ivgtt every 3 weeks).

Interventions

Paclitaxel

paclitaxel 80 mg/m\^2 ivgtt d1, d8, d15, 28 days per cycle, 6 cycles.

Intervention Type: DRUG

Carboplatin

carboplatin AUC=2 ivgtt d1, d8, d15, 28 days per cycle, 6 cycles.

Intervention Type: DRUG

Epirubicin

epirubicin 90 mg/m\^2 ivgtt d1, 21 days per cycle, 4 cycles.

Intervention Type: DRUG

Cyclophosphamide

cyclophosphamide 600 mg/m\^2 iv d1, 21 days per cycle, 4 cycles.

Intervention Type: DRUG

Trastuzumab

trastuzumab 6 mg/kg (loading dose 8mg/kg) ivgtt d1, 21 days per cycle with chemotherapy; or trastuzumab 2 mg/kg (loading dose 4mg/kg, w1) ivgtt d1, d8, d15, d22, 28 days per cycle with chemotherapy. After chemotherapy, patient will continue to complete 1 year of adjuvant trastuzumab (6 mg/kg ivgtt every 3 weeks).

Intervention Type: DRUG

Pertuzumab

pertuzumab 420mg (loading dose 840mg) ivgtt d1, 21 days per cycle with chemotherapy. After chemotherapy, patient will continue to complete 1 year of adjuvant pertuzumab (420mg ivgtt every 3 weeks).

Intervention Type: DRUG

Docetaxel

docetaxel 100 mg/m\^2 ivgtt d1, 21 days per cycle, 4 cycles.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Female patients aged 18-70 years old;

2. Histologically confirmed unilateral invasive breast cancer (regardless of pathological type)

3. Operable breast cancer at first diagnosis, without any absolute surgical contraindication.

4. No gross nor microscopic residual tumor after surgery.

5. HER2-positive with ≥ 1 positive axillary lymph node; or estrogen receptor (ER) and/or progesterone receptor (PR)-positive and HER2-negative with ≥ 4 positive axillary lymph node. HER2-positive is defined as an immunohistochemistry (IHC) status of 3+, or a positive in situ hybridization (Fluorescence in situ hybridization (FISH), Chromogenic in situ hybridization (CISH)) test. ER-positive is defined as immunohistochemistry showing that ≥ 1% of tumor cells were ER positive. PR-positive is defined as immunohistochemistry showing that ≥ 1% of tumor cells were PR positive.

6. Preoperative examination found no evidence of metastasis in clinical examination nor imaging examination.

7. No peripheral neuropathy.

8. Karnofsky score > 70.

9. Good postoperative recovery, at least 1 week has passed since most recent surgery.

10. Has adequate bone marrow function: leukocyte count > 4x10ˆ9 / L, absolute neutrophil count > 2x10ˆ9 /L; platelet count > 100x10ˆ9 /L, hemoglobin > 9g/dL.

11. Has adequate liver function: alanine aminotransferase (ALT) < 1.5×upper limit of normal (ULN), aspartate aminotransferase (AST) < 1.5×ULN, alkaline phosphatase (AKP) < 2.5×ULN, total bilirubin (TBIL) < 1.5×ULN.

12. Has adequate kidney function: serum creatinine < 1.5×ULN.

13. Contraception during treatment for women of childbearing age.

14. Has adequate cardiac function: echocardiography showed left ventricular ejection fraction (LVEF) > 50%.

15. Participants voluntarily joined the study, has signed informed consent before any trial related activities are conducted, has good compliance and has agreed to follow-up.

Exclusion Criteria

1. Has received previous chemotherapy for late stage disease.

2. Has bilateral breast cancer or bilateral carcinoma in situ.

3. Has metastatic (Stage 4) breast cancer.

4. Has clinical T4 lesion (UICC1987) (with skin involvement, mass adhesion and fixation, and inflammatory breast cancer).

5. Has received neoadjuvant therapy (include chemotherapy, targeted therapy, radiotherapy or endocrine therapy).

6. Has previous history of additional malignancy(with the exception of adequately treated basal cell carcinoma and cervical carcinoma in situ), including contralateral breast cancer.

7. Is already participating in another clinical trial.

8. Has severe systemic disease and/or uncontrolled infection.

9. Has insufficient cardiac function: echocardiography showed LVEF< 50%.

10. Has suffered from severe cardiovascular and cerebrovascular diseases disease within the 6 months previous of randomization (such as unstable angina, chronic heart failure, uncontrolled hypertension with blood pressure>150/90 mmHg, myocardial infarction, or cerebrovascular accident.

11. Has known allergy to chemotherapy drugs used in this study.

12. Is pregnant, is breast feeding, or is a woman of childbearing age who cannot practice effective contraceptives during treatment and until 8 weeks after the end of treatment.

13. Has entered the study, but pre-treatment examination showed a positive pregnancy test.

14. Has a history of mental disorders, cognitive impairment, inability to understand the study protocol and side effects, inability to complete the study protocol and follow-up workers (systematic evaluation is required before the patient is enrolled into the study), or is without independent civil capacity.

15. The researchers judged patients to be unsuitable for the study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Fudan University

OTHER

Sponsor Role: lead

Responsible Party

Zhimin Shao

Professor, Key Laboratory of Breast Cancer in Shanghai, Department of Breast Surgery

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

ZhiMin Shao, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Fudan University

Locations

Cancer Hospital Affiliated to Fudan University

Shanghai, Shanghai Municipality, China

Countries

China

Other Identifiers

2018-68-1461

Identifier Type: -

Identifier Source: org_study_id