MedPath

Trial Studying Chemotherapy in Nigerian Women With Triple Negative Breast Cancer

Phase 2
Not yet recruiting
Conditions
Triple Negative Breast Cancer
Interventions
Registration Number
NCT06291064
Lead Sponsor
University of Chicago
Brief Summary

The primary purpose of this study is to determine what proportion of participants will achieve complete pathological response with epirubicin+ cyclophosphamide followed by docetaxel +carboplatin. This will also examine the potential of using signals in the blood (biomarkers) to identify resistance to chemotherapy in Nigerian women with triple negative breast cancer (TNBC).

All enrollment to this trial will occur at sites in Nigeria. University of Chicago is serving as coordinating center and will be involved in data analysis.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
Female
Target Recruitment
85
Inclusion Criteria
  1. Women ages of 18 to 70 years old

  2. Women who are able and willing to read understand and sign an informed consent document

  3. Biopsy-accessible breast tumor of significant size for core needle biopsy/ultrasound measurable (≥ 2cm)

  4. Patients with histologically confirmed carcinoma of the female breast with triple-negative status by immunohistochemistry (IHC). Patients who are low estrogen reception (ER) expression (< 20%), progesterone receptor (PR) negative and human epidermal growth factor 2 (HER2) negative are eligible.

  5. Clinical stages IIA -IIIC (AJCC 2009)

  6. Chemotherapy-naïve patients (for this cancer)

  7. Performance status: Eastern Cooperative Oncology Group (ECOG) performance status 0-1

  8. Non-pregnant and not nursing.

    • Granulocyte greater than or equal to 1,500/microliter
    • Platelet count greater than or equal to 100,000/microliter
    • Absolute neutrophil count (ANC) greater than or equal to l500/microliter
    • Hemoglobin greater than or equal to 10g/deciliter
    • Bilirubin less than or equal 1.5 x upper limit of normal
    • aspartate aminotransferase (ALT or SGOT) and alanine transaminase (AST or SGPT) less than 2.5 x upper limit of normal
  9. Creatinine within institutional normal limits or glomerular filtration rate greater than or equal to 30 mL/min/1.73 m2 by Chronic Kidney Disease Epidemiology Collaboration (CKD EPI) equation 10. Baseline left ventricular ejection fraction of greater than or equal to 55%

Exclusion Criteria
  1. Pregnant or lactating women.
  2. Patients with distant metastasis (brain and/or visceral metastasis)
  3. Serious, uncontrolled, concurrent infection(s).
  4. Treatment for other carcinomas within the last 5 years, except non-melanoma skin cancer and treated cervical carcinoma in-situ (CCIS)
  5. Participation in any investigational drug study within 4 weeks preceding the start of study treatment
  6. Other serious uncontrolled medical conditions that the treating investigator feels might compromise study participation including but not limited to chronic or active infection, HIV-positive patient, uncontrolled hypertension, symptomatic congestive heart failure, unstable angina pectoris, uncontrolled diabetes mellitus, or psychiatric illness/social situations that would limit compliance with study requirements.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Treatment ArmCyclophosphamideParticipants will receive epirubicin and cyclophosphamide every three weeks for a total of 12 weeks followed by 3-weekly docetaxel for 12 weeks and carboplatin every three weeks for a total of 12 weeks. All premenopausal participants will receive luteinizing hormone-releasing hormone (LHRH) agonist goserelin (Zoladex) for contraception and fertility preservation.
Treatment ArmBreast SurgeryParticipants will receive epirubicin and cyclophosphamide every three weeks for a total of 12 weeks followed by 3-weekly docetaxel for 12 weeks and carboplatin every three weeks for a total of 12 weeks. All premenopausal participants will receive luteinizing hormone-releasing hormone (LHRH) agonist goserelin (Zoladex) for contraception and fertility preservation.
Treatment ArmEpirubicinParticipants will receive epirubicin and cyclophosphamide every three weeks for a total of 12 weeks followed by 3-weekly docetaxel for 12 weeks and carboplatin every three weeks for a total of 12 weeks. All premenopausal participants will receive luteinizing hormone-releasing hormone (LHRH) agonist goserelin (Zoladex) for contraception and fertility preservation.
Treatment ArmDocetaxelParticipants will receive epirubicin and cyclophosphamide every three weeks for a total of 12 weeks followed by 3-weekly docetaxel for 12 weeks and carboplatin every three weeks for a total of 12 weeks. All premenopausal participants will receive luteinizing hormone-releasing hormone (LHRH) agonist goserelin (Zoladex) for contraception and fertility preservation.
Treatment ArmCarboplatinParticipants will receive epirubicin and cyclophosphamide every three weeks for a total of 12 weeks followed by 3-weekly docetaxel for 12 weeks and carboplatin every three weeks for a total of 12 weeks. All premenopausal participants will receive luteinizing hormone-releasing hormone (LHRH) agonist goserelin (Zoladex) for contraception and fertility preservation.
Treatment ArmCapecitabineParticipants will receive epirubicin and cyclophosphamide every three weeks for a total of 12 weeks followed by 3-weekly docetaxel for 12 weeks and carboplatin every three weeks for a total of 12 weeks. All premenopausal participants will receive luteinizing hormone-releasing hormone (LHRH) agonist goserelin (Zoladex) for contraception and fertility preservation.
Primary Outcome Measures
NameTimeMethod
Percentage of Participants that Achieve Pathologic Complete Response (pCR) Rate (Breast)4 - 6 months from start of chemotherapy

How well does the study chemotherapy regimen of epirubicin and cyclophosphamide (EC) followed by docetaxel and carboplatin work to remove tumor cells in the breast. This will be determined by percentage of participants that do not have noticeable cancer cells in the breast after completing the chemotherapy regimen.

Percentage of Participants that Achieve Pathologic Complete Response (pCR) Rate (Lymph Nodes)4 - 6 months from start of chemotherapy

How well does the study chemotherapy regimen of epirubicin and cyclophosphamide (EC) followed by docetaxel and carboplatin work to remove tumor cells in the lymph nodes. This will be determined by percentage of participants that do not have noticeable cancer cells in the lymph nodes after completing the chemotherapy regimen.

Percentage of Participants that Achieve Pathologic Complete Response (pCR) Rate (By Stage)4 - 6 months from start of chemotherapy

How well does the study chemotherapy regimen of epirubicin and cyclophosphamide (EC) followed by docetaxel and carboplatin work to remove tumor cells based on stage of breast cancer. This will be determined by percentage of participants that do not have noticeable cancer cells in the lymph nodes after completing the chemotherapy regimen.

Secondary Outcome Measures
NameTimeMethod
Heart Related Side Effects of the Pre-Surgery Chemotherapy Regimen10 years from start of treatment

Percentage of participants with Heart failure (NYHA Class III or IV or as confirmed by a cardiologist) and a decrease in left ventricular ejection fraction (LVEF) of at least 10 ejection fraction (EF) points from baseline and to below 50%.

Clinical Response4 - 6 months from start of chemotherapy

Percentage of participants achieving clinical response (CR and PR) during neoadjuvant period by breast ultrasound

Invasive Disease Free Survival (iDFS)10 years from start of treatment

Time to cancer returning or death

Side Effects of the Study Pre-surgery Chemotherapy RegimenAfter 8 cycles of treatment (24 weeks)

Percentage of participants experiencing Grades 3 and 4 blood, gastrointestinal, neurological and cardiovascular toxicities.

Progressive DiseaseAfter 8 cycles of treatment (24 weeks)

Percentage of participants with progressive disease during pre-surgery treatment period

Duration of Response10 years from start of treatment

Time to cancer worsening or death

© Copyright 2025. All Rights Reserved by MedPath