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A Phase III, Adjuvant Trial Comparing Three Chemotherapy Regimens in Women With Node-Positive Breast Cancer: Docetaxel/Doxorubicin/Cyclophosphamide (TAC); Dose-Dense (DD) Doxorubicin/Cyclophosphamide Followed By DD Paclitaxel (DD AC→P); DD AC Followed By DD Paclitaxel Plus Gemcitabine (DD AC→PG)

Phase 3
18 Years
Open (Enrolling)
Breast Cancer

Thank you

Trial Information

A Phase III, Adjuvant Trial Comparing Three Chemotherapy Regimens in Women With Node-Positive Breast Cancer: Docetaxel/Doxorubicin/Cyclophosphamide (TAC); Dose-Dense (DD) Doxorubicin/Cyclophosphamide Followed By DD Paclitaxel (DD AC→P); DD AC Followed By DD Paclitaxel Plus Gemcitabine (DD AC→PG)



- Compare disease-free survival in women with node-positive breast cancer treated with 3
different adjuvant chemotherapy regimens comprising dose-dense doxorubicin,
cyclophosphamide, paclitaxel, and gemcitabine vs docetaxel, doxorubicin, and
cyclophosphamide vs dose-dense doxorubicin, cyclophosphamide, and paclitaxel.


- Compare overall survival, recurrence-free interval, and distant recurrence-free
interval, in patients treated with these regimens.

- Compare the toxic effects of these regimens in these patients.

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to
number of positive lymph nodes (1-3 vs 4-9 vs ≥ 10), hormone receptor status (estrogen
receptor [ER]- and progesterone receptor [PgR]- negative vs ER- and/or PgR-positive), type
of prior surgery and planned radiotherapy (lumpectomy and local radiotherapy [RT] without
regional RT vs lumpectomy and local RT with regional RT vs mastectomy without RT vs
mastectomy with local or regional RT). Patients are randomized to 1 of 3 treatment arms.

- Group 1: Patients receive doxorubicin IV over 15 minutes, cyclophosphamide IV over 30
minutes, and docetaxel IV over 1 hour on day 1. Treatment repeats every 21 days for 6

- Group 2: Patients receive AC chemotherapy comprising doxorubicin IV over 15 minutes and
cyclophosphamide IV over 30 minutes on day 1. Treatment repeats every 14 days for 4
courses. Beginning 14 days after the last dose of AC, patients receive paclitaxel IV
over 3 hours on day 1. Treatment repeats every 14 days for 4 courses.

- Group 3: Patients receive AC chemotherapy as in Group 2. Beginning 14 days after the
last dose of AC, patients receive paclitaxel as in Group 2 and gemcitabine IV over
30-60 minutes on day 1. Treatment repeats every 14 days for 4 courses.

In all arms, treatment continues in the absence of disease progression or unacceptable

Beginning 3-12 weeks after the last dose of chemotherapy, patients with ER-positive and/or
PgR-positive tumors receive hormonal therapy.

Beginning no sooner than 3 weeks after the last dose of chemotherapy, patients treated with
lumpectomy undergo whole-breast radiotherapy. Patients treated with mastectomy may undergo
chest wall and/or regional nodal radiotherapy.

Patients are followed every 6 months for 5 years and then annually thereafter.

PROJECTED ACCRUAL: A total of 4,800 patients will be accrued for this study within 4 years.

Inclusion Criteria:

- The patient must consent to participate in the study and must have signed an approved
consent form conforming with federal and institutional guidelines.

- The patient must have a life expectancy of at least 10 years and a Zubrod performance
status of 0 or 1. (Comorbid conditions but not the diagnosis of breast cancer should
be taken into consideration when determining life expectancy.)

- The interval between the last surgery for breast cancer staging or treatment and
randomization must be no more than 84 days.

- The tumor must be invasive carcinoma of the breast on histologic examination.

- All of the following staging criteria must be met:

- By clinical and pathologic evaluation, primary tumor must be T1-3;

- By clinical evaluation, ipsilateral nodes must be cN0, cN1, or cN2a;

- By pathologic evaluation, ipsilateral nodes must be pN1 (pN1mi, pN1a, pN1b,
pN1c), pN2a, pN3a, or pN3b (only if due to microscopic involvement of internal
mammary node detected by sentinel lymph node dissection and with more than 3
positive axillary lymph nodes).

- Patients must have an estrogen receptor (ER) analysis performed on the primary tumor
prior to randomization. If ER analysis is negative, then progesterone receptor (PgR)
analysis must be performed. If ER analysis is positive, PgR analysis is desired, but
not mandatory. ("Marginal" or "borderline" results [i.e., those not definitely
negative] will be considered positive regardless of the methodology used.)

- Patients must have had either a lumpectomy or a total mastectomy. Patients must have
completed one of the following procedures for evaluation of pathologic nodal status.

- Sentinel lymphadenectomy followed by removal of additional non-sentinel lymph
nodes (This approach is strongly recommended.)

- Sentinel lymphadenectomy alone if one of the following criteria is met:

- Pathologic nodal staging based on sentinel lymphadenectomy is pN1mi or pN1b

- Surgeon elects not to remove additional non-sentinel nodes (This approach is
strongly discouraged, but will not preclude participation in B-38.)

- Axillary lymphadenectomy without sentinel node isolation procedure.

- Patients must have no clinical or radiologic evidence of metastatic disease.

- Patients with either skeletal pain or alkaline phosphatase that is greater than ULN
but less than or equal to 2.5 x ULN are eligible for inclusion in the study if bone
scans fail to demonstrate metastatic disease. Suspicious findings on bone scan must
be confirmed as benign by x-ray, MRI, or biopsy.

- Patients with aspartate transaminase (AST) or alkaline phosphatase greater than ULN
are eligible for inclusion in the study if liver imaging fails to demonstrate
metastatic disease and the following requirements are met at the time of

- Postoperative absolute granulocyte count (AGC) must be greater than or equal to

- Postoperative platelet count must be greater than or equal to 100,000/mm3.

- The following criteria for postoperative evidence of adequate hepatic function
must be met:

- total bilirubin must be less than or equal to ULN for the lab unless the
patient has a grade 1 bilirubin elevation (greater than ULN to 1.5 x ULN)
due to Gilbert's disease or similar syndrome due to slow conjugation of
bilirubin; and

- alkaline phosphatase must be less than or equal to 2.5 x ULN for the lab;

- the AST must be less than or equal to 1.5 x ULN for the lab; and

- alkaline phosphatase and AST cannot both be greater than ULN.

- Postoperative serum creatinine must be less than or equal to ULN.

- At the time of randomization, the patient must have had the following: history and
physical exam, EKG, and imaging of the chest within the past 3 months and bilateral
mammogram within the past 6 months.

- Within 3 months prior to entry, the patient must have a baseline left ventricular
ejection fraction (LVEF), measured by Multiple Gated Acquisition (MUGA) scan or
echocardiogram, greater than or equal to lower limit of normal (LLN) for the facility
performing the procedure and no evidence of regional wall abnormalities.

- Patients with a history of non-breast malignancies are eligible if they have been
disease-free for 5 or more years prior to randomization and are deemed by their
physician to be at low risk for recurrence. Patients with the following cancers are
eligible if diagnosed and treated within the past 5 years: carcinoma in situ of the
cervix, carcinoma in situ of the colon, melanoma in situ, and basal cell and squamous
cell carcinoma of the skin.

- Special conditions for eligibility of lumpectomy patients: radiation therapy and
surgery. Patients treated by lumpectomy must meet all the eligibility criteria in
addition to the following:

- Generally, lumpectomy should be reserved for tumors less than 5 cm. However, at
the investigator's discretion, patients treated with lumpectomy for tumors
greater than or equal to 5 cm are eligible if eligibility criteria for
lumpectomy are met.

- The margins of the resected specimen must be histologically free of invasive
tumor and DCIS as determined by the local pathologist. In patients for whom
pathologic examination demonstrates tumor present at the line of resection,
additional operative procedures may be performed to obtain clear margins. This
is permissible even if axillary evaluation has been completed. Patients in whom
tumor is still present at the resected margin after re-excision(s) must undergo
total mastectomy to be eligible. (Patients with margins positive for lobular
carcinoma in situ (LCIS) are eligible without additional resection.)

- Irradiation of regional lymph nodes is optional, but plans for radiation therapy
must be declared by the investigator prior to randomization for stratification

- Special conditions for eligibility of mastectomy patients: radiation therapy o
Postmastectomy chest wall and/or regional nodal irradiation is optional. Plans for
radiation in mastectomy patients must be declared by the investigator prior to
randomization for stratification purposes.

Ineligibility Criteria

- Male patients are not eligible for this study. Women with one or more of the
following conditions or prior therapies are also ineligible for this study:

- Tumor that has been determined to be human epidermal growth factor receptor 2
(HER2)-positive by immunohistochemistry (3+) or by fluorescent in situ hybridization
(positive for gene amplification).

- Contralateral breast cancer (invasive or DCIS) or a mass or mammographic abnormality
in the opposite breast suspicious for malignancy unless there is biopsy proof that
the mass is not malignant.

- Primary tumor staged as T4 for any reason.

- Clinical nodal stages including cN2b and cN3 or pathologic nodal stages including
pN0(i+), pN2b, pN3b with clinically apparent internal mammary nodes, or pN3c.

- Suspicious nodes in the contralateral axilla or suspicious supraclavicular nodes.
Patients with these conditions are considered ineligible unless there is biopsy
evidence that these are not involved with tumor.

- Prior history of breast cancer, including DCIS (patients with a history of LCIS are

- Treatment, including radiation therapy, chemotherapy, and/or hormonal therapy
administered for the currently diagnosed breast cancer prior to randomization. One
exception is hormonal therapy, which may have been given for up to a total of 28 days
anytime after diagnosis and before study entry. In such a case, hormonal therapy
must stop at or before randomization and be re-started, if indicated, following
chemotherapy. A second exception is radiation therapy for patients enrolled in NSABP
B-39 and assigned to partial breast irradiation (Group 2). These patients may have
received RT prior to B-38 study entry.

- Prior therapy with anthracyclines or taxanes for any malignancy.

- Any sex hormonal therapy, e.g., birth control pills, ovarian hormonal replacement
therapy, etc. (These patients are eligible if this therapy is discontinued prior to

- Therapy with any hormonal agents such as raloxifene (Evista®), tamoxifen, or other
selective estrogen-receptor modulators (SERMs), either for osteoporosis or breast
cancer prevention. (Patients are eligible only if these medications are discontinued
prior to randomization.

- Cardiac disease that would preclude the use of anthracyclines. This includes:

- history of myocardial infarction documented by elevated cardiac enzymes or
regional wall abnormalities on assessment of left ventricular (LV) function;

- angina pectoris that requires the use of anti-anginal medication;

- any history of documented congestive heart failure;

- serious cardiac arrhythmia requiring medication;

- severe conduction abnormality;

- valvular disease with documented cardiac function compromise; and

- uncontrolled hypertension defined as blood pressure greater than 160/100 on
antihypertensive therapy.

- Conditions that would prohibit administration of corticosteroids.

- Sensory/motor neuropathy greater than or equal to grade 2, as defined by the NCI's
Common Terminology Criteria for Adverse Events Version 3.0.

- Non-malignant systemic disease (cardiovascular, renal, hepatic, etc.) that would
preclude a patient from receiving any of the treatment options or would prevent
prolonged follow-up.

- History of hepatitis B or C.

- Pregnancy or lactation at the time of proposed randomization. Women of reproductive
potential must agree to use an effective non-hormonal method of contraception.

- Concurrent treatment with other investigational agents for the treatment of breast

- Psychiatric or addictive disorders or other conditions that, in the opinion of the
investigator, would preclude the patient from meeting the study requirements.

- Special conditions for ineligibility of lumpectomy patients: radiation therapy and

- For patients treated by lumpectomy, whole breast irradiation is required.

- The following patients will be ineligible:

- Patients with diffuse tumors (as demonstrated on mammography) treated with
lumpectomy. (These patients are eligible if they undergo mastectomy.)

- Patients treated with lumpectomy in whom there is another clinically dominant
mass or mammographically suspicious abnormality within the ipsilateral breast
remnant. Such a mass must be biopsied and demonstrated to be histologically
benign prior to randomization or, if malignant, must be surgically removed with
clear margins.

- Patients in whom the margins of the resected specimen are involved with invasive
tumor or DCIS.

Type of Study:


Study Design:

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Disease-free survival: any recurrence, contralateral breast cancer, second primary cancer, death from any cause prior to recurrence or second primary cancer

Outcome Time Frame:

Every 6 months for 5 years and then annually thereafter.

Safety Issue:


Principal Investigator

Sandra M. Swain, MD

Investigator Role:

Study Chair

Investigator Affiliation:

Washington Hospital Center


United States: Federal Government

Study ID:




Start Date:

October 2004

Completion Date:

March 2016

Related Keywords:

  • Breast Cancer
  • stage II breast cancer
  • stage IIIA breast cancer
  • stage IIIC breast cancer
  • Breast Neoplasms



CCOP - Northern New Jersey Hackensack, New Jersey  07601
Blumenthal Cancer Center at Carolinas Medical Center Charlotte, North Carolina  28232-2861
Lucille P. Markey Cancer Center at University of Kentucky Lexington, Kentucky  40536-0093
Madigan Army Medical Center - Tacoma Tacoma, Washington  98431
Methodist Estabrook Cancer Center Omaha, Nebraska  68114-4199
Community Oncology Group at Cleveland Clinic Cancer Center Independence, Ohio  44131
Altru Cancer Center at Altru Hospital Grand Forks, North Dakota  58201
Lurleen Wallace Comprehensive Cancer at University of Alabama - Birmingham Birmingham, Alabama  35294
Providence Cancer Center Anchorage, Alaska  99508
South Shore Hospital South Weymouth, Massachusetts  02190
Robert and Carol Weissman Cancer Center at Martin Memorial Stuart, Florida  34994
Chestnut Hill Healthcare Cancer Center Philadelphia, Pennsylvania  19118