A Randomized Trial of Ixempra Versus Taxol in Adjuvant Therapy of Triple Negative Breast Cancer

Patients will be randomized in a 1:1 ratio to receive one of two different treatment arms.
Patients in treatment arm 1 will receive AC followed by ixabepilone. Patients in treatment
arm 2 will receive AC followed by weekly paclitaxel.

Inclusion Criteria:

1. Female patients greater than or equal to18 years of age.

2. Histologically confirmed invasive unilateral breast cancer (regardless of

histology).

3. Early-stage breast cancer, defined as:

- Node-positive disease: >0.2-mm metastasis in at least one lymph node
(pN1mipN2b)OR

- Node-negative, with primary tumor >1.0 cm (T1c-T3).

4. Definitive loco-regional surgery must have been completed as specified

below:

- Patients must have undergone either breast conservation surgery

(i.e., lumpectomy) or total mastectomy.

- Surgical margins of the resected section must be histologically free of

invasive adenocarcinoma and ductal carcinoma in situ.

- Surgical margins involved with lobular carcinoma in situ (LCIS) will not

be considered as a positive margin; therefore, such patients will be eligible for
this study without additional resection.

- Patients must have completed axillary lymph node sampling for the pathologic
evaluation of axillary lymph nodes as specified below:

Sentinel node biopsy and/or either lymph node sampling procedure or axillary
dissection.

5. Multicentric and multifocal invasive breast cancer is eligible if loco-regional
surgery has been completed as described above.

6. Patients with synchronous bilateral cancers are eligible only if:

- All cancers are of triple-negative phenotype, defined as ER-, PR-, HER2-.

- Eligibility based on the highest stage grouping.

7. HER2 negative tumors. HER2 negativity must be confirmed by one of the

following:

- FISH-negative (FISH ratio <2.2), or

- IHC 0-1+, or

- IHC 2-3+ AND FISH-negative (FISH ratio <2.2).

8. Estrogen receptor negative (<10% staining by IHC for estrogen receptor).

9. Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1.

10. Patient must be <= 84 days from having completed definitive primary breast surgery
(either lumpectomy or mastectomy).

11. MammoSite brachytherapy radiation is acceptable if it is performed

immediately following surgery and prior to chemotherapy. It is recommended that
chemotherapy be started no earlier than 2 weeks following the removal of the
MammoSite balloon catheter.

12. Adequate hematologic function, defined by:

- Absolute neutrophil count (ANC) >1500/mm3

- Platelet count >=100,000/mm3

- Hemoglobin >9 g/dL

13. Adequate liver function, defined by:

- AST and ALT <=2.5 x the upper limit of normal (ULN)

- Total bilirubin <=1.5 x ULN (unless the patient has grade 1 bilirubin

elevation due to Gilbert's disease or a similar syndrome involving slow

conjugation of bilirubin).

14. Adequate renal function, defined by:

- Serum creatinine <=1.5 x ULN

15. Complete staging work-up <=12 weeks prior to initiation of study treatment

with computed tomography (CT) scans of the chest and abdomen/pelvis (abdomen/pelvis
preferred; abdomen accepted), and either a positron emission tomography (PET) scan or
a bone scan.

16. Adequate cardiac function, defined by a left ventricular ejection fraction

(LVEF) value of >50% (or normal per institutional guidelines) by MUGA scan or
echocardiogram (ECHO).

17. Adequate recovery from recent surgery. At least 1 week must have elapsed from the
time of a minor surgery (i.e., sentinel node biopsy, port-acath (placement); at least
3 weeks must have elapsed from the time of a major surgery (i.e., lumpectomy, partial
or total mastectomy, axillary lymph node dissection, breast reconstruction
procedure).

18. Patients with previous history of invasive cancers (including breast cancer)

are eligible if definitive treatment was completed more than 5 years prior to

initiating current study treatment, and there is no evidence of recurrent disease.

19. Women of childbearing potential must have a negative serum or urine pregnancy test
performed within 7 days prior to start of treatment. If a woman becomes pregnant or
suspects she is pregnant while participating in this study, she must agree to inform
her treating physician immediately.

20. Patient must be accessible for treatment and follow-up.

21. Women of childbearing potential must agree to use an acceptable method of birth
control to avoid pregnancy for the duration of study treatment, and for 3 months
thereafter.

22. All patients must be able to understand the investigational nature of the

study and give written informed consent prior to study entry.

Exclusion Criteria:

1. Women who are pregnant or breastfeeding.

2. History of previous diagnosis of invasive breast cancer (unless treated >5 years
previously with no recurrence). History of previously treated ductal carcinoma in
situ (DCIS) is acceptable.

3. Any evidence or suspicion of metastatic disease other than ipsilateral

axillary lymph nodes.

4. Any tumor >=T4 (cutaneous invasion, deep adherence, inflammatory breast cancer).

5. Previous anthracycline chemotherapy.

6. Concurrent use of CYP3A4 inhibitors from 72 hours prior to initiation of

study treatment until the end of treatment with ixabepilone.

7. Previous treatment for this breast cancer (including neoadjuvant

chemotherapy).

8. Previous cancer (with the exception of non-melanoma skin cancer or cervical carcinoma
in situ) in the past 5 years (including invasive contralateral breast cancer).

9. Peripheral neuropathy of > grade 1 per NCI CTCAE v3.0.

10. Cardiac disease, including: congestive heart failure (CHF) > Class II per

New York Heart Association (NYHA) classification; unstable angina (anginal symptoms
at rest) or new-onset angina (i.e., began within the last 3 months), or myocardial
infarction within the past 6 months; symptomatic CHF, unstable angina pectoris,
cardiac arrhythmia, or cardiac ventricular arrhythmias requiring anti-arrhythmic
therapy.

11. History of hypersensitivity to CremophorEL (polyoxyethylated castor oil) or

a drug formulated in CremophorEL such as paclitaxel.

12. Use of any investigational agent within 30 days of administration of the first dose
of study drug.

13. Patients may not receive any other investigational or anti-cancer treatments while
participating in this study.

14. Concurrent severe, uncontrolled infection or intercurrent illness including,

but not limited to, ongoing or active infection, or psychiatric illness/social

situations that would limit compliance with study requirements.

15. Mental condition that would prevent patient comprehension of the nature of, and risk
associated with, the study.

16. Inability to comply with study and/or follow-up procedures.