The Trial Comparing Dose-dense AC-T With TP as Adjuvant Therapy for TNBC With Homologous Recombination Repair Deficiency

NCT ID: NCT03876886

Last Updated: 2019-03-21

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE3
• Total Enrollment: 200 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-02-22
• Study Completion Date: 2024-12-31

Brief Summary

The purpose of this trial is to compare the 3-year disease-free survival of dose-dense epirubicin and cyclophosphamide followed by paclitaxel with paclitaxel plus carboplatin as adjuvant therapy for triple-negative breast cancer with homologous recombination repair deficiency.

The other purpose of this trial is to observe the patient's tolerance.

Detailed Description

Triple-negative breast cancer (TNBC) lack the expression of oestrogen receptor (ER), progesterone receptor(PR) and human epidermal growth factor receptor 2 (HER2) , and characterizes an aggressive behavior with higher risk of recurrence and death compared to other breast cancer subtypes. Little therapeutic progress has been made in adjuvant therapy in TNBC during the past decades and the standard of care is still missing.

Pre-clinical and clinical data suggest that platinum-based regimens represent an emerging therapeutic option for selected patients with homologous recombination repair deficiency (HRD). The HR system is critical in regulating and maintaining genome stability, and is one of the most commonly altered systems in TNBCs, up to 15-20% TNBC patients carry germline BRCA1/2 mutations. Other HR genes included PALB2, RAD51 etc. Tumors that harbor HRD possess an increased burden of genomic aberrations and lesions, and have been shown to have increased sensitivity to DNA crosslinking agents such as platinum salts. Platinum-based regimens have been encouraging in TNBC patients with HRD, given increases in both pathologic complete response (pCR) rates in neoadjuvant trials and objective response rates(ORR) in metastatic diseases. Further information are needed on how platinum-containing therapies affect long-term outcomes in the adjuvant setting.

In this trial, the investigators intend to compare the 3-year disease-free survival (DFS) of dose-dense epirubicin and cyclophosphamide followed by paclitaxel with paclitaxel plus carboplatin as adjuvant therapy in high-risk node-negative or node-positive TNBC patients with HRD. The other purpose of this trial is to observe the participants' tolerance.

Conditions

Triple Negative Breast Cancer

Study Design

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

Study Groups

AC-T(dose-dense)

A: epirubicin, pharmorubicin (EPI) C: cyclophosphamide (CTX） T: paclitaxel (PTX）

Group Type: ACTIVE_COMPARATOR

Epirubicin

Intervention Type: DRUG

Epirubicin 90mg/m2 iv d1 or divide into two days

Cyclophosphamide

Intervention Type: DRUG

cyclophosphamide600mg/m2 iv d1,q14d\*4cycles;with G-CSF support: 3ug/kg ih

Paclitaxel

Intervention Type: DRUG

paclitaxel 175mg/m2 iv d1, q14d\*4cycles

TP(dose-dense)

T: paclitaxel (PTX） P: carboplatin (CBP)

Group Type: EXPERIMENTAL

Carboplatin

Intervention Type: DRUG

carboplatin AUC=3 iv d2, q14d\*8cycles;with G-CSF support: 3ug/kg ih

Paclitaxel

Intervention Type: DRUG

paclitaxel 175mg/m2 iv d1, q14d\*8cycles

Interventions

Epirubicin

Epirubicin 90mg/m2 iv d1 or divide into two days

Intervention Type: DRUG

Cyclophosphamide

cyclophosphamide600mg/m2 iv d1,q14d\*4cycles;with G-CSF support: 3ug/kg ih

Intervention Type: DRUG

Paclitaxel

paclitaxel 175mg/m2 iv d1, q14d\*4cycles

Intervention Type: DRUG

Carboplatin

carboplatin AUC=3 iv d2, q14d\*8cycles;with G-CSF support: 3ug/kg ih

Intervention Type: DRUG

Paclitaxel

paclitaxel 175mg/m2 iv d1, q14d\*8cycles

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. 18-60 years

2. Histologically confirmed adenocarcinoma of the breast, complete tumor removal by either modified radical mastectomy or local excision plus axillary lymph node dissection (i.e., breast conservation therapy) or sentinel node biopsy. (Tumor-free margins at least 1 mm for both invasive and noninvasive carcinoma except for lobular carcinoma in situ (less than 1 mm allowed);

3. Histologically confirmed ER(-) PR(-) and HER-2(IHC(immunohistochemistry) 0-1+ or FISH (fluorescence in situ hybridization) negative)

4. Next-generation sequencing confirmed homologous recombination repair deficiency

5. Meet one of the following criteria:

(1) Positive axillary lymph nodes; (2) Negative axillary lymph nodes with at least one of the following risk factors: age<= 35 years; grade III; infiltrative tumor size > 2cm; intravascular tumor embolus; Ki-67>=50%.

6. Eastern Cooperative Oncology Group (ECOG) Performance Score 0-1 7. Adequate bone marrow reserve with ANC > 1500, HGB > 9g/dL and platelets > 100,000.

8. Adequate renal function with serum creatinine < 2.0. 9. Adequate hepatic reserve with serum bilirubin < 2.0, AST/ALT < 2X the upper limit of normal, and alkaline phosphatase < 5X the upper limit of normal. Serum bilirubin > 2.0 is acceptable in the setting of known Gilbert's syndrome.

10. Not pregnant, and on appropriate birth control if of child-bearing potential.

11. Written informed consent according to the local ethics committee requirements.

Exclusion Criteria

1. Prior systemic treatment of breast cancer, including chemotherapy;

2. Metastatic breast cancer;

3. Patients with medical conditions that indicate intolerant to adjuvant therapy and related treatment, including uncontrolled pulmonary disease, diabetes mellitus, severe infection, active peptic ulcer, coagulation disorder, connective tissue disease or myelo-suppressive disease;

4. Has active hepatitis B or hepatitis C with abnormal liver function tests (LFTs) or is known to be HIV positive;

5. Contraindication for using dexamethasone;

6. History of congestive heart failure, uncontrolled or symptomatic angina pectoris, arrhythmia or myocardial infarction; poorly controlled hypertension (systolic BP>180 mmHg or diastolic BP>100 mmHg);

7. Pregnant or breast feeding.

8. Hepatic, renal, or bone marrow dysfunction as detailed above.

9. Known severe hypersensitivity to any drugs in this study;

10. Treatment with any investigational drugs within 30 days before the beginning of study treatment.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Chinese Academy of Medical Sciences

OTHER

Sponsor Role: lead

Responsible Party

Binghe Xu

Professor of Medical Oncology

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

National Cancer Center, Cancer Hospital/Chinese Academy of Medical Sciences and Peking Union Medical College

Beijing, Beijing Municipality, China

Site Status: RECRUITING

Countries

China

Central Contacts

Binghe Xu

Role: CONTACT

xubinghe@medmail.com.cn

+86-10-87788120

Qing Li

Role: CONTACT

cheryliqing@hotmail.com

+86-10-87788120

Facility Contacts

Binghe XU, M.D.

Role: primary

xubinghe@medmail.com.cn

86-10-88788826

Other Identifiers

BXu-1839

Identifier Type: -

Identifier Source: org_study_id