For Healthcare Professionals

Ixabepilone in Treating Participants With Significant Residual Disease of HER2/Neu Negative Invasive Breast Cancer After Systemic Therapy

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About the study

This phase II trial studies how well ixabepilone compared with standard of care works in treating patients with HER2/Neu negative breast cancer that remains after undergoing systemic therapy. Ixabepilone works by blocking cell division which may cause cancer cell death.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

  1. Patients with histologic confirmation of invasive HER2/neu-negative breast cancer (immunohistochemistry [IHC] 0-1+ or fluorescence in situ hybridization [FISH]-negative) that have received complete anthracycline and taxane neoadjuvant systemic therapy and that at the time of surgery are expected to have significant residual disease. Therapy should include at least 4 cycles of an anthracycline-based regimen (adriamycin-cytoxan [AC], 5-fluorouracil/adriamycin/intravenous [IV] cyclophosphamide [FAC], fluorouracil-epirubicin-IV cytoxan [FEC]) and 12 weeks of a taxane-based regimen (weekly paclitaxel, every 3-week docetaxel).
  2. Patients who did not complete therapy due to disease progression are eligible.
  3. Patients with bilateral breast cancers are eligible.
  4. Patients should have a Karnofsky performance scale of >= 70%.
  5. Peripheral granulocyte count of >= 1500/mm^3.
  6. Platelet count >= 100000 mm^3.
  7. Bilirubin within normal laboratory values.
  8. Alkaline phosphatase may be up to 1.5 x upper limit of normal (ULN) of the institution.
  9. Transaminases (alanine aminotransferase [ALT] and aspartate aminotransferase [AST]) may be up to 1.5 x upper limit of normal (ULN) of the institution.
  10. Creatinine levels within normal range.
  11. Negative serum pregnancy test for a woman of childbearing potential.
  12. Women of childbearing potential (WOCP) must use a reliable and appropriate contraceptive method during the study and 6 months after chemotherapy is completed. Women of childbearing potential (WOCBP) are women who are not menopausal for 12 months or had no previous surgical sterilization.
  13. Patients must agree to have study tissue collections and blood sample collections.
  14. Patients must sign an informed consent indicating that they are aware of the investigational nature of the study, in keeping with institutional policy.
  15. Patients should have their surgical tissues evaluated for residual cancer burden (RCB) and be used for correlative studies.
  16. Sexually active women of childbearing potential must use an effective method of birth control during the course of the study, in a manner such that risk of failure is minimized. Prior to study enrollment, women of childbearing potential (WOCBP) must be advised of the importance of avoiding pregnancy during trial participation and the potential risk factors for an unintentional pregnancy. In addition, men enrolled on this study should understand the risks to any sexual partner of childbearing potential and should practice an effective method of birth control.
  17. All WOCBP MUST have a negative pregnancy test within 7 days prior to first receiving investigational product. If the pregnancy test is positive, the patient must not receive investigational product and must not be enrolled in the study. In addition, all WOCBP will be instructed to contact the Investigator immediately if they suspect they might be pregnant (e.g., missed or late menstrual period) at any time during study participation. The principal investigator (PI) will immediately notify BMS in the event of a confirmed pregnancy in a patient participating in the study.

EXCLUSION CRITERIA

  1. Patients whose tumors express HER2 protein or have HER2/neu gene amplification.
  2. Patients with a history of other invasive malignancies diagnosed and treated within the previous 5 years, except non-melanoma skin cancer and non-invasive cervical cancer.
  3. Other concurrent severe and/or uncontrolled medical disease which could compromise participation in the study (i.e., uncontrolled diabetes, uncontrolled hypertension, severe infection, severe malnutrition, unstable angina, or congestive heart failure
  4. New York Heart Association Class III or IV, ventricular arrhythmias, active ischemic heart disease, myocardial infarction within six months, chronic liver or renal disease, active upper gastrointestinal [GI] tract ulceration).
  5. Patients with a pre-existing peripheral neuropathy > grade 1.
  6. Evidence of distant metastases.
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Study Locations

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How to Apply


Contact the study center to learn if this study is a good match for you.

Study’s details


Contition

Bilateral Breast Carcinoma,Breast Cancer,HER2/Neu Negative,Invasive Breast Carcinoma

Age

18+

Phase

Phase 2

Participants needed

116

Est. Completion Date

Dec 2024

Treatment type

Interventional


Sponsor

M.D. Anderson Cancer Center

ClinicalTrials.gov identifier

NCT00877500

Study number

20080435

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