Breast Cancer, Metastatic Breast Cancer
Conditions
Brief summary
This trial combines dose dense chemotherapy with doxorubicin and cyclophosphamide (AC) followed by standard, every 3 week docetaxel and GW572016 (lapatinib) for neoadjuvant treatment of Her2neu positive stage II/III breast cancer. The purpose of the study was to determine whether lapatinib combined with chemotherapy was safe and resulted in an increase in pathologic complete response rates.
Detailed description
Lapatinib acts as a dual inhibitor of both epidermal growth factor receptor (EGFR) and ErbB-2 (Her2/neu) tyrosine kinase activity. EGFR and ErbB2 receptors are frequently over-expressed or altered in human cancers including breast cancer. This study plans to determine the antitumor activity of this regimen and its effectiveness preventing tumor growth and spread. Neoadjuvant chemotherapy which achieves pathologic complete responses (pCR) has been shown to predict improved long-term survival and serves as a surrogate for clinical outcome. By using this primary endpoint we can obtain statistical data with smaller patient numbers and at a lower overall cost. Additionally, we hope to correlate clinical and radiologic outcomes with gene expression data.
Interventions
DRUGLapatinib
1250 mg, tablets, oral daily during treatment with docetaxel (3-week cycles x 4 cycles)
DRUGDoxorubicin
60 mg/m2, intravenously every 2 weeks for 4 cycles. Given as first treatment with cyclophosphamide.
DRUGCyclophosphamide
600 mg/m2, intravenously every 2 weeks for 4 cycles. Given as first treatment with doxorubicin.
DRUGDocetaxel
100 mg/m2, intravenously every 3 weeks for 4 cycles (after treatment cycles of doxorubicin and cyclophosphamide
DRUGPegfilgrastim
6 mg, subcutaneously on day 2 of all cytotoxic chemotherapy treatments.
DRUGFilgrastim
300 or 480 mcg, subcutaneously on days 3 to 10 after cytotoxic chemotherapies.
DRUGDexamethasone
8 mg, oral taken twice a day for 3 days starting 24 hours before docetaxel
DRUGTrastuzumab
Loading dose 8 mg/kg, then 6 mg/kg, intravenously every 3 weeks for 1 year
Sponsors
GlaxoSmithKline
Sanofi
George Albert Fisher
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
* Female * Histologically-confirmed Her2neu positive breast cancer, by either Immunohistochemistry (IHC) 3+ or Fluorescence In Situ Hybridization (FISH)+ * Stage II/III breast cancer including any large primary tumor (\> 2 cm), tumors of any size associated with skin or chest wall involvement, tumors of any size with axillary lymph node involvement, (T2-T4, N0-N2) and those with ipsilateral subclavicular or supraclavicular lymph nodes). * At least one bi-dimensional, measurable indicator lesion. * Between 18 and 70 years of age * Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2 / Karnofsky ≥ 60% at screening and on the first day of treatment. * Informed consent must be obtained prior to registration. * Cardiac ejection fraction within the institutional range of normal as measured by multigated acquisition (MUGA) or echocardiography (ECHO) scan. * Absolute neutrophil count \> 1,500/mm³ * Hemoglobin \> 8.0 g/dL * Platelet count \> 100,000/mm³ * Creatinine within normal institutional limits * Total Bilirubin equal to or less than institutional upper limit of normal (ULN) * Aspartate aminotransferase (AST); alanine aminotransferase (ALT); and alkaline phosphatase must be within the range allowing for eligibility. In determining eligibility the more abnormal of the two values (AST or ALT) should be used. * Eligibility of patients receiving medications or substances known to affect, or with the potential to affect the activity or pharmacokinetics of GW572016 will be determined following review of their use by the Principal Investigator * Antacid use is prohibited 1 hour before and 1 hour after GW572016 dosing. * All herbal (alternative) medicines are prohibited. * Medications prohibited during the administration of lapatinib . * Women of child-bearing potential must have negative pregnancy test and must agree to use adequate contraception (hormonal or barrier method of birth control or abstinence) prior to study entry and for the duration of study participation. * Peripheral neuropathy: must be \< grade 1 * Able to swallow and retain oral medication
Exclusion criteria
* Evidence of disease outside the breast or chest wall, except for ipsilateral axillary , supraclavicular, or infraclavicular lymph nodes. * Prior chemotherapy, immunotherapy, or hormonal therapy for breast cancer. * More than 3 months between histologic diagnosis and registration on this study. * History of other malignancy within the last 5years, except curatively treated basal cell carcinoma of the skin or carcinoma in situ of the cervix. * Psychological, familial, sociological or geographical conditions which do not permit weekly medical follow-up and compliance with the study protocol. Those who are medically-unstable, including but not limited to active infection, acute hepatitis, deep vein thrombosis requiring anticoagulant therapy, gastrointestinal bleeding, uncontrolled hypercalcemia, uncontrolled diabetes, dementia, seizures, superior vena cava syndrome, and those whose circumstances do not permit completion of the study or the required follow-up. * Congestive heart failure, abnormal left ventricular ejection fraction (LVEF), angina pectoris, uncontrolled cardiac arrhythmias, or other significant heart disease, or who have had a myocardial infarction within the past year. * Pregnant or lactating * Of childbearing potential and not employing adequate contraception * History of allergic reactions attributed to compounds of similar chemical or biologic composition to GW572016. * HIV-positive and receiving combination anti-retroviral therapy are excluded from the study because of possible pharmacokinetic interactions with lapatinib. Appropriate studies will be undertaken in patients receiving combination anti-retroviral therapy when indicated. * GI tract disease resulting in an inability to take oral medication, malabsorption syndrome, a requirement for IV alimentation, prior surgical procedures affecting absorption, uncontrolled inflammatory GI disease (e.g., Crohn's, ulcerative colitis). * History of severe hypersensitivity reaction to taxotere or other drugs formulated with polysorbate 80. * Current active hepatic or biliary disease (with exception of patients with Gilberts syndrome, asymptomatic gallstones, or stable chronic liver disease per investigator assessment ).
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Percentage of Participants With Pathologic Complete Response (pCR) | 12 weeks | Pathologic Complete Response (pCR) rate, assessed as no evidence of invasive disease in excised surgical specimens of breast and/or axilla, in participants who received at least 1 cycle of docetaxel and lapatinib and at least one follow-up evaluation. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Disease-free Survival (DFS) | 42 months (median follow-up) | Disease-free survival (DFS) is expressed as the percentage of participants who were disease-free and alive at the time of analysis. |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Neoadjuvant Chemotherapy Doxorubicin (Adriamycin) + cyclophosphamide (Cytoxan) with pegfilgrastim or filgrastim growth factor support every 2 weeks for 4 cycles, followed by docetaxel + lapatinib for four 21-day cycles, followed by surgery. Dexamethasone was administered twice-a-day for 3 days, starting 24 hours before the docetaxel infusions. After surgery +/- radiation, participants may receive trastuzumab (Herceptin) for a year. | 21 |
| Total | 21 |
Withdrawals & dropouts
| Period | Reason | FG000 |
|---|---|---|
| Overall Study | Withdrawal by Subject - Adverse event | 2 |
| Overall Study | Withdrawal by Subject - Pre-treatment | 1 |
Baseline characteristics
| Characteristic | Neoadjuvant Chemotherapy |
|---|---|
| Age, Categorical <=18 years | 0 Participants |
| Age, Categorical >=65 years | 2 Participants |
| Age, Categorical Between 18 and 65 years | 19 Participants |
| Ethnicity (NIH/OMB) Hispanic or Latino | 2 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 19 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants |
| Histology Ductal | 21 Participants |
| Histology Lobular | 0 Participants |
| Nodal involvement N1 (few lymph nodes) | 3 Participants |
| Nodal involvement N2 (moderate number of lymph nodes) | 13 Participants |
| Nodal involvement N3 (many lymph nodes) | 5 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants |
| Race (NIH/OMB) Asian | 8 Participants |
| Race (NIH/OMB) Black or African American | 0 Participants |
| Race (NIH/OMB) More than one race | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants |
| Race (NIH/OMB) White | 13 Participants |
| Sex: Female, Male Female | 21 Participants |
| Sex: Female, Male Male | 0 Participants |
| Tumor Size T1 (≤ 20 mm at widest) | 0 Participants |
| Tumor Size T2 (> 20 mm but ≤ 50 mm) | 9 Participants |
| Tumor Size T3 (> 50 mm) | 9 Participants |
| Tumor Size T4 (metastatic to chest wall / skin) | 3 Participants |
Adverse events
| Event type | EG000 affected / at risk |
|---|---|
| deaths Total, all-cause mortality | 2 / 21 |
| other Total, other adverse events | 21 / 21 |
| serious Total, serious adverse events | 0 / 21 |
Outcome results
Primary
Percentage of Participants With Pathologic Complete Response (pCR)
Pathologic Complete Response (pCR) rate, assessed as no evidence of invasive disease in excised surgical specimens of breast and/or axilla, in participants who received at least 1 cycle of docetaxel and lapatinib and at least one follow-up evaluation.
Time frame: 12 weeks
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Neoadjuvant Chemotherapy | Percentage of Participants With Pathologic Complete Response (pCR) | 38.9 percentage of participants |
Secondary
Disease-free Survival (DFS)
Disease-free survival (DFS) is expressed as the percentage of participants who were disease-free and alive at the time of analysis.
Time frame: 42 months (median follow-up)
Population: DFS is reported as the number and percentage of participants who were alive and disease-free at the time of analysis.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Neoadjuvant Chemotherapy | Disease-free Survival (DFS) | 16 Participants |