Study of Utidelone Based Neoadjuvant Treatment on Early High-risk or Locally Advanced Breast Cancer

NCT ID: NCT05983094

Last Updated: 2023-08-09

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 181 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-09-01
• Study Completion Date: 2027-09-01

Brief Summary

The purpose of this clinical trial is to evaluate the efficacy and safety of Utidelone based regimen as neoadjuvant treatment With High-risk Early-stage or Locally Advanced Breast Cancer.

Detailed Description

This is a single arm, multi-center study,three-cohort, prospective phase II study which will enroll 181 high-risk early-stage or locally advanced breast cancer patients.

Conditions

Breast Cancer; Neoadjuvant Therapy

Study Design

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

Study Groups

cohort 1 Triple-negative breast cancer

Hormone Receptor(HR) negative, Human Epidermal Growth Factor Receptor 2(HER2 )negative breast cancer Drug: Utidelone in combination with carboplatin Utidelone injection 30mg/m2, on days 1-5 of each cycle; Carboplatin ,Area Under Curve(AUC)6, iv, was administered on day 1; One treatment cycle is 21 days, and there are 6 cycles in total.

Group Type: EXPERIMENTAL

Utidelone

Intervention Type: DRUG

Utidelone injection 30mg/m2, on days 1-5 of each cycle

Carboplatin

Intervention Type: DRUG

Carboplatin Area under curve(AUC)6, iv, was administered on day 1

cohort 2 HR positive, HER2 negative breast cancer

HR positive, HER2 negative, Immunohistochemical(IHC)0,1+; 2+, Fluorescence in situ hybridization(FISH)non-amplification breast cancer Drug: Utidelone in combination with Epirubicin Utidelone injection 30mg/m2, on days 1-5 of each cycle; Epirubicin 75mg/m2 was administered on day 1; One treatment cycle is 21 days, and there are 6 cycles in total.

Group Type: EXPERIMENTAL

Utidelone

Intervention Type: DRUG

Utidelone injection 30mg/m2, on days 1-5 of each cycle

Epirubicin

Intervention Type: DRUG

Epirubicin 75mg/m2 was administered on day 1

cohort 3 HER2 positive (IHC 3+; IHC 2+,FISH amplification) breast cancer

Drug: Utidelone in combination with carboplatin, trastuzumab and pertuzumab Utidelone injection 30mg/m2, on days 1-5 of each cycle; Carboplatin Area Under Curve(AUC)6, iv, was administered on day 1; One treatment cycle is 21 days, and there are 6 cycles in total. Trastuzumab 8mg/kg iv in first cycle on day 1, then 8mg/kg in the rest cycles; pertuzumab 840mg/kg iv in first cycle on day 1, then 420mg/kg in the rest cycles.

One treatment cycle is 21 days, and there are 6 cycles in total.

Group Type: EXPERIMENTAL

Utidelone

Intervention Type: DRUG

Utidelone injection 30mg/m2, on days 1-5 of each cycle

Carboplatin

Intervention Type: DRUG

Carboplatin Area under curve(AUC)6, iv, was administered on day 1

Trastuzumab

Intervention Type: DRUG

Trastuzumab 8mg/kg iv in first cycle on day 1, then 6mg/kg in the rest cycles

Pertuzumab

Intervention Type: DRUG

Pertuzumab 840mg/kg iv in first cycle on day 1, then 420mg/kg in the rest cycles

Interventions

Utidelone

Utidelone injection 30mg/m2, on days 1-5 of each cycle

Intervention Type: DRUG

Carboplatin

Carboplatin Area under curve(AUC)6, iv, was administered on day 1

Intervention Type: DRUG

Epirubicin

Epirubicin 75mg/m2 was administered on day 1

Intervention Type: DRUG

Trastuzumab

Trastuzumab 8mg/kg iv in first cycle on day 1, then 6mg/kg in the rest cycles

Intervention Type: DRUG

Pertuzumab

Pertuzumab 840mg/kg iv in first cycle on day 1, then 420mg/kg in the rest cycles

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Female patients who will receive initial treatment, 18-70 years of age；

2. Newly diagnosed high-risk early stage (T1c-2, N1; T2, N0) and locally advanced (T1c-2, N2-3; T3-4, N0-3) breast cancer (tumor stage II, III), in which HR+/HER2- T2, N0 patients need to be accompanied by high-risk factors (histological grade 3 or Ki67 ≥ 20%). Triple negative breast cancer(TNBC), HER2 positive (Immunohistochemical(IHC)3+; IHC 2+, FISH amplification) breast cancer, HR negative HER2 IHC 2+ and undetermined result of FISH, HR positive HER2 negative (IHC 0,1+; 2+, FISH amplification) breast cancer confirmed by pathological test.

3. Eastern Cooperative Oncology Group(ECOG) performance status 0 or 1

4. The blood routine examination was basically normal (CTCAE ≤ 1) within one week before enrollment (based on the normal values of each research center laboratory). No Human Granulocyte Colony Stimulating Factor(rhGCSF) or blood transfusion/erythropoietin(EPO) or other drugs were used within 14 days prior to enrollment.

White blood cell count (WBC) ≥ 4 x109 / L; Neutrophil count (ANC) > 1.5x109 / L; Platelet count (PLT) ≥ 100×109/L Hemoglobin(Hb) ≥ 100g/L.

5. The blood biochemistry examination was basically normal (CTCAE ≤ 1) within one week before enrollment (based on the normal values of each research center laboratory) Serum total bilirubin ≤ Upper limit of normal value(ULN)； Aspartate aminotransferase (AST) and Alanine aminotransferase (ALT) ≤ 1.5×ULN； Alkaline phosphatase ≤ 2.5×ULN； Serum creatinine ≤ 1.5×ULN.

6. Color Doppler echocardiography left ventricular Ejection fraction (LVEF) ≥ 55%

7. Female patients with fertility must agree to use effective contraceptive methods during the study period and within 6 months of the last study medication. The Pregnancy test (urine or serum) must be negative

8. Be willing and able to provide written informed consent/assent for the trial.

Exclusion Criteria

1. Primary stage IV breast cancer；

2. Inflammatory breast cancer;

3. Bilateral primary breast cancer (including invasive cancer and carcinoma in situ)；

4. Previous anti-cancer treatment or radiotherapy for any malignant tumor, excluding cured cervical Carcinoma in situ, skin Basal-cell carcinoma and squamous cell carcinoma.

5. Receive any sex hormone treatment (such as contraceptives, ovarian hormone replacement therapy, etc.), except for Ovarian function suppression（OFS）fertility protection, or any hormone drugs (such as Raloxifene, tamoxifen, or other selective estrogen receptor modulators) to treat osteoporosis or prevent breast cancer；

6. The patient has undergone major surgery unrelated to breast cancer within 4 weeks before treatment or has not yet fully recovered;

7. Symptomatic peripheral neuropathy CTCAE 5.0 grade ≥ 2

8. Serious cardio cerebral Vascular disease, including but not limited to the followings:

9. History of congestive heart failure or systolic dysfunction (LVEF<50%);

10. Angina pectoris requiring anti angina drugs;

11. High risk uncontrolled arrhythmias or severe conduction abnormalities, such as ventricular arrhythmias that require clinical intervention, II-III degree atrioventricular block, etc; Under resting state, the average corrected Q-T interval(QTcF) of three 12 lead electrocardiogram examinations is>470ms;

12. Clinically significant heart valve disease with cardiac dysfunction;

13. Hypertension that cannot be controlled;

14. History of myocardial infarction

15. Allergic to any component of any drug in this protocol.

16. Those who are not suitable for using Corticosteroid.

17. Individuals with active infections who currently require systematic anti infection treatment.

18. History of immune deficiency disease, including positive of HIV/AIDS, or other acquired or congenital immune deficiency diseases, or having a history of organ transplantation.

19. Who had participated in other drug intervention clinical trials within the 28 days of randomization, or who is participating in another clinical trial or is using other investigational treatments.

20. Individuals in pregnancy (positive Pregnancy test) and lactation.

21. Any other comorbidities that interfere with the implementation of the treatment plan, or the researcher evaluate that the subject has a history of other serious systemic diseases, or other reasons lead to the patients is unsuitable to participate in this trial.

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

Sponsors

Chinese Academy of Medical Sciences

OTHER

Sponsor Role: collaborator

Cancer Hospital Chinese Academy of Medical Science, Shenzhen Center

OTHER

Sponsor Role: collaborator

First Affiliated Hospital of China Medical University

UNKNOWN

Sponsor Role: collaborator

Cancer Institute and Hospital, Chinese Academy of Medical Sciences

OTHER

Sponsor Role: lead

Responsible Party

Ma Fei，MD

Deputy Director of the Department of Medical Oncology

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Cancer Hospital, Chinese Academy of Medical Sciences

Beijing, Beijing Municipality, China

Countries

China

Other Identifiers

NCC4047

Identifier Type: -

Identifier Source: org_study_id