Breast Cancer
Conditions
Keywords
Adjuvant therapy, Bevacizumab, Abraxane, Early stage breast cancer
Brief summary
The primary objective of this study was to compare the safety of dose-dense ABI-007 (Abraxane) 260 mg/m\^2 or Taxol 175 mg/m\^2 given every 2 weeks following dose-dense Adriamycin plus Cytoxan (AC) chemotherapy. Bevacizumab was administered at 10 mg/kg every 2 weeks throughout chemotherapy, and then at 15 mg/kg every 3 weeks following chemotherapy.
Interventions
DRUGAdriamycin and Cytoxan (AC)
Adriamycin (doxorubicin) and Cytoxan (cyclophosphamide) make up the chemotherapy regimen known as AC. Adriamycin 60 mg/m\^2 intravenous, plus Cytoxan 600 mg/m\^2 intravenous on Day 1 of each of four 2-week cycles (weeks 1-8).
DRUGABI-007
260 mg/m\^2 IV on day 1 of each of four 2-week cycle, representing treatment cycles 5-8 (weeks 9-16)
DRUGTaxol
175 mg/m\^2 intravenously (IV) on day 1 of each of four 2-week cycle, representing treatment cycles 5-8 (weeks 9-16)
DRUGBevacizumab
10 mg/kg on day 1 of each of eight 2-week cycles (weeks 9-16), then 15 mg/kg on day 1 of each of ten three-week cycles (weeks 17-46).
DRUGpegfilgrastim
6 mg subcutaneous (SC) on day 2 for each of the first four 2-week cycles (weeks 1-8). Pegfilgrastim 6 mg SC was administered on day 2 of cycles 6-8 (weeks 11-16) during taxane treatment only if necessary.
Sponsors
Celgene
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
A patient was eligible for inclusion in this study only if all of the following criteria were met: 1. Female, age greater than or equal to 18 to less than or equal to 70 years old. 2. Estrogen receptor (ER) and progesterone receptor (PR) status have been determined. 3. Operable, histologically confirmed adenocarcinoma of the breast 4. Must have met 1 of the following criteria: * T1-3, N1-3, M0, regardless of ER or PR status. * T \> 2 cm, N0, M0 (T2-3N0M0), regardless of ER or PR status. * T \> 1 cm, N0, M0 (T1cN0M0) and both ER and PR negative * T \> 1 cm, N0, M0, ER or PR positive and grade 3 5. Patients with one sentinel lymph node metastasis 0.2-2 mm in size were not required to undergo completion axillary dissection unless only 1 sentinel lymph node was examined. This completion axillary dissection was optional if 1 out of 2 or more sentinel lymph nodes was positive for a micrometastasis. Therefore if 1 of 1 sentinel lymph node was positive for micrometastasis(0.2-2 mm), then a completion axillary dissection was required. 6. Patients with more than one sentinel node micrometastasis or 1 node with a micrometastasis \> 2 mm and/or T3 disease must have undergone completion, standard axillary dissection. -Note: the following were not eligible- T1b,c,N0M0 and ER or PR positive and grade 1 or 2 Tx tumors (regardless of nodal status) T4 disease \[i.e., patients with fixed tumors, peau d'orange skin changes, skin ulcerations, or inflammatory changes * Note: Sentinel lymph node micrometastasis \< 0.2 mm in considered N0 disease 7. Negative surgical margins on lumpectomy or mastectomy specimen (no ink on invasive cancer and no ink on ductal carcinoma in situ \[DCIS\]). 8. Eastern Cooperative Oncology Group (ECOG) performance status 0-1 9. Normal electrocardiogram (ECG, as assessed by the investigator). 10. No pre-existing peripheral neuropathy. 11. It had not been longer than 84 days since the date of definitive surgery (eg, mastectomy or in the case of a breast-sparing procedure, axillary dissection). 12. Laboratory values were to be as follows: * White blood cell count: \> or equal to 3,000/mm\^3 * Absolute neutrophil count:\> or equal to 1,500/mm\^3 * Platelets:\> or equal to 100,000/mm\^3 * Hemoglobin: \> or equal to 8g/dL * Bilirubin:\< or equal to the institution's ULN * Creatinine: \< or equal to 1.7 mg/dL * Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) and alkaline phosphatase could be up to 2.5 times the institutional ULN. 13. All staging studies including physical exam, chest x-ray, and bone scan had to show no evidence of metastatic disease, including suspicious lymphadenopathy or skin nodules on physical exam. A chest x-ray and bone scan were mandatory; however, all other staging studies were at the treating physician's discretion. Any other staging test (eg, Computed Tomography \[CT\] scans, magnetic resonance imaging \[MRI\] studies, ultrasound of abdomen, Positron Emission Tomography \[PET\] scans must have been negative for metastatic disease. An abdominal CT scan or PET scan was mandatory for patients with liver function tests elevated above the upper limit of normal (ULN) to rule out metastatic disease. If the patient had a staging PET scan then a bone scan was not necessary, but a chest x-ray was required. 14. Patient had a negative serum pregnancy test \< or equal to 14 days of the first dose of study drug (patients of childbearing potential). 15. If fertile, patient had agreed to us an acceptable method of birth control to avoid pregnancy \[Note: oral contraceptives were not allowed\] for the duration of chemotherapy and hormonal therapy and for 6 months thereafter. 16. If obese, a patient must have been treated with doses calculated using his/her actual body surface area (BSA) (the physician must have been comfortable treating at the full BSA dose regardless of BSA). 17. Patient had signed a Patient Informed Consent Form.
Exclusion criteria
A patient was not eligible for inclusion in this study if any of the following criteria applied: 1. Patients with HER-2 positive breast cancer (IHC 3+ or FISH +) who were eligible for adjuvant Herceptin therapy. 2. Stage IV breast cancer (M1 disease on TNM staging system). 3. Prior anthracycline, anthracenedione (mitoxantrone), or taxane therapy 4. Neoadjuvant therapy for this breast cancer. 5. Previous invasive cancers if treated \< 5 years prior to entering this study, except basal or squamous cell carcinoma of the skin or carcinoma in situ of the cervix; the latter were not required to have occurred more than 5 years prior to study entry. 6. Prior invasive breast cancer if diagnosed \< 5 years prior to entering study. Patients must have finished adjuvant hormonal therapy prior to registration. Patients with prior DCIS are eligible. Patients with DCIS who were treated with tamoxifen must have finished tamoxifen prior to registration. 7. Serious medical illness, other than that treated by this study, which would limit survival to \< 4 years, or psychiatric condition that would prevent informed consent and compliance with study treatment. 8. Uncontrolled or severe cardiovascular disease including recent (\< or equal to 12 months) myocardial infarction or unstable angina. 9. Active uncontrolled bacterial, viral (including clinically defined Acquired Immune Deficiency Syndrome \[AIDS\]), or fungal infection. 10. Patients with active or chronic hepatitis with abnormal liver function tests (LFTs) or patients who were known to be HIV positive. 11. Uncontrolled disease such as uncontrolled diabetes. 12. Any prior history of hypertensive crisis or hypertensive encephalopathy. 13. Any known central nervous system (CNS) disease. 14. Known hypersensitivity to any component of bevacizumab. 15. No history of cerebrovascular accident or transient ischemic attack at any time. 16. Active symptomatic vascular disease, e.g., aortic aneurysm or aortic dissection, and no peripheral vascular disease, e.g., claudication, within six months of study entry. 17. No major surgical procedure, open biopsy, or significant traumatic injury within 28 days and no core biopsy or minor surgical procedure (excluding placement of a vascular access device) within seven days of study entry. No anticipated need for major surgical procedure during the course of study. 18. No history of abdominal fistula, gastrointestinal perforation, or intra- abdominal process within six months of study entry. 19. No serious non-healing wound, ulcer, or bone fracture. 20. No proteinuria at screening as demonstrated by urine protein: urine creatinine (UPC) ratio of \> or equal to 1.0 or urine dipstick for proteinuria \> or equal to 2+ (patients discovered to have \> or equal to 2+ proteinuria on dipstick urinalysis at baseline should have undergone a 24 hour urine collection and must have demonstrated \< or equal to 1g of protein in 24 hours to be eligible). 21. Inadequately controlled hypertension (defined as systolic blood pressure \> 150 mmHg and /or diastolic blood pressure\> 100 mmHg on antihypertensive medications) or New York Heart Association (NYHA) Grade 2 or greater congestive heart failure. 22. History or coagulopathy, bleeding diathesis, therapeutic anticoagulation other than low dose or chronic acetyl salicylic acid (ASA)\> or equal to 325 mg. per day. Low dose coumadin for anticoagulation of venous access device or low dose molecular weight heparin (LMWH) for deep vein thrombosis prophylaxis or low dose (325 mg or less) ASA prophylaxis are allowed, but are best avoided if the treating physician feels it is safe to do so. 23. Left Ventricular Ejection Fraction (LVEF) on cardiac echocardiography (ECHO) \< 50% (or institutional lower limit of normal \[LLN\]) and \> or equal to 74%. LVEF of greater than 75% at baseline should have been re- reviewed and/or the test repeated as it could be falsely elevated. 24. Patients who were receiving concurrent immunotherapy. 25. A history of other malignancy within the last 5 years, which could affect the diagnosis or assessment of breast cancer recurrence or which could shorten a patient's survival. 26. Patient had had an organ allograft. 27. Patient was pregnant or breastfeeding. 28. Patient was unable to comply with requirements of study. 29. Patient was receiving any other investigational drugs.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Month 7 | Toxicities are summarized using the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) terms. Participants with treatment-emergent toxicities with a frequency of \>=20% in any treatment arm, and participants with at least one toxicity are reported. Taxane subsets (ABI-007 subset and Taxol subset treatment arms) summarize participants with treatment-emergent toxicities defined as any AEs that begin or worsen in severity grade after the start of taxane treatment (cycle 5, week 9) through 30 days after the last dose of taxane (week 20) and were ongoing 3 months after chemotherapy (month 7). Entire regiments (AC --\> ABI-007 and AC --\> Taxol treatment arms) summarize participants with treatment-emergent toxicities defined as any AEs that begin or worsen in severity grade after the start of chemotherapy (cycle 1, week 1) through 30 days after the last dose of chemotherapy (week 20) and were ongoing 3 months after chemotherapy (month 7). |
| Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Month 10 | Toxicities are summarized using the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) terms. Participants with treatment-emergent toxicities with a frequency of \>=20% in any treatment arm, and participants with at least one toxicity are reported. Taxane subsets (ABI-007 subset and Taxol subset treatment arms) summarize participants with treatment-emergent toxicities defined as any AEs that begin or worsen in severity grade after the start of taxane treatment (cycle 5, week 9) through 30 days after the last dose of taxane (week 20) and were ongoing 6 months after chemotherapy (month 10). Entire regiments (AC --\> ABI-007 and AC --\> Taxol treatment arms) summarize participants with treatment-emergent toxicities defined as any AEs that begin or worsen in severity grade after the start of chemotherapy (cycle 1, week 1) through 30 days after the last dose of chemotherapy (week 20) and were ongoing 6 months after chemotherapy (month 10). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Percent of Protocol Taxane Dose | approximately week 9-16 | Percent of the protocol-defined taxane (ABI-007 or Taxol) dose that was actually taken by study participants. |
| Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | up to Week 46 | Counts of participants who * completed the protocol-defined treatment cycles, * had a dose interruption * had a dose reduction * had a dose delay. A dose delay refers to the delay of all interventions in the cycle. Dose modifications are typically caused by clinically significant laboratory abnormalities and /or treatment emergent adverse events/toxicities. Use of pegfilgrastim is included in the summary. |
| The Cumulative Dose of Taxane Delivered During Study | approximately week 9-16 | The cumulative dose of taxane (Taxol or ABI-007) taken during the study (cycles 4-8 which is approximately weeks 9-16). |
| Change From Baseline in Percent Left Ventricular Ejection Fraction (% LVEF) at the Final Evaluation | up to week 46 | Decreased left ventricular ejection fraction (LVEF) is an indication of cardiotoxicity. Change from baseline measurements to the final evaluation are summarized. |
| Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | Week 1 up to week 50 | Summary of the most severe grades using the National Cancer Institute's Common Terminology Criteria for Adverse Events v3.0 (CTCAE) for the following liver and renal function tests. Grade 0 = within normal range for all measurements. Alkaline phosphatase, alanine aminotransferase (ALT), aspartate aminotransferase (AST): * Grade 1 = \> upper limit of normal (ULN) - 2.5\*ULN * Grade 2= \>2.5-5.0\*ULN * Grade 3= \>5.0-20.0\*ULN * Grade 4= \>20.0\*ULN Bilirubin: * Grade 1= \>ULN - 1.5\*ULN * Grade 3= \>3.0 - 10.0\*ULN Creatinine: \- Grade 1= \>ULN - 1.5\*ULN |
| Myelosuppression During Taxane Dosing Cycles | Weeks 9-16 | Myelosuppression represented by neutropenia (low absolute neutrophil counts (ANC)) with severity grades according to Common Terminology Criteria for Adverse Events v3.0 (CTCAE). * Grade 1 = \<lower limit of normal (LLN)-1.5\*10\^9/L * Grade 2 = \<1.5 - 1.0\*10\^9/L * Grade 3 = \<1.0 - 0.5\*10\^9/L * Grade 4 = \<0.5\*10\^9/L Values are reported across all severity grades without assessment of relationship to taxane treatment, and also by relation to taxane treatment as reported by investigators. |
| Mean Taxane Dose Intensity Per Week | approximately week 9-16 | Cumulative taxane (ABI-007 or Taxol) dose divided by the number of weeks on taxane treatment. |
Countries
United States
Participant flow
Recruitment details
Multicenter study
Pre-assignment details
Two hundred three patients were randomized and one hundred ninety-seven were treated.
Participants by arm
| Arm | Count |
|---|---|
| AC --> ABI-007 Adriamycin and Cytoxan plus Bevacizumab for four cycles (weeks 1-8); 260 mg/m\^2 ABI-007 (Abraxane) plus Bevacizumab for four cycles (weeks 9-16); Bevacizumab (weeks 17-46). | 98 |
| AC --> Taxol Adriamycin and Cytoxan plus Bevacizumab for four cycles (weeks 1-8); 175 mg/m\^2 Taxol plus Bevacizumab for four cycles (weeks 9-16); Bevacizumab (weeks 17-46). | 99 |
| Total | 197 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 |
|---|---|---|---|
| Overall Study | Adverse Event | 7 | 5 |
| Overall Study | Non-compliance, pt moved, pt/inv agree | 2 | 2 |
| Overall Study | Physician Decision | 1 | 1 |
| Overall Study | Protocol Violation | 0 | 1 |
| Overall Study | Unacceptable Toxicity | 20 | 18 |
| Overall Study | Withdrawal by Subject | 7 | 11 |
Baseline characteristics
| Characteristic | AC --> Taxol | Total | AC --> ABI-007 |
|---|---|---|---|
| Age, Continuous | 51.2 years STANDARD_DEVIATION 9.29 | 51.2 years STANDARD_DEVIATION 9.23 | 51.2 years STANDARD_DEVIATION 9.21 |
| Age, Customized < 65 years | 88 participants | 177 participants | 89 participants |
| Age, Customized >=65 years | 11 participants | 20 participants | 9 participants |
| Eastern Cooperative Oncology Group (ECOG) Performance Status 0 (Fully active) | 89 participants | 178 participants | 89 participants |
| Eastern Cooperative Oncology Group (ECOG) Performance Status 1 (Restrictive but ambulatory) | 10 participants | 19 participants | 9 participants |
| Estrogen Receptor Status Negative | 33 participants | 68 participants | 35 participants |
| Estrogen Receptor Status Positive | 66 participants | 129 participants | 63 participants |
| Menopausal Status postmenopausal | 55 participants | 103 participants | 48 participants |
| Menopausal Status premenopausal | 44 participants | 94 participants | 50 participants |
| Physician's Assessment of Peripheral Neuropathy 0 (None) | 96 participants | 190 participants | 94 participants |
| Physician's Assessment of Peripheral Neuropathy 1 | 0 participants | 1 participants | 1 participants |
| Physician's Assessment of Peripheral Neuropathy Not reported | 3 participants | 6 participants | 3 participants |
| Progesterone Receptor Status Negative | 40 participants | 79 participants | 39 participants |
| Progesterone Receptor Status Positive | 59 participants | 118 participants | 59 participants |
| Race/Ethnicity, Customized Asian | 2 participants | 5 participants | 3 participants |
| Race/Ethnicity, Customized Black, of African heritage | 7 participants | 17 participants | 10 participants |
| Race/Ethnicity, Customized Other | 1 participants | 2 participants | 1 participants |
| Race/Ethnicity, Customized White, Hispanic or Latino | 17 participants | 25 participants | 8 participants |
| Race/Ethnicity, Customized White, non-Hispanic, non-Latino | 72 participants | 148 participants | 76 participants |
| Region of Enrollment United States | 99 participants | 197 participants | 98 participants |
| Sex: Female, Male Female | 99 Participants | 197 Participants | 98 Participants |
| Sex: Female, Male Male | 0 Participants | 0 Participants | 0 Participants |
| Stage at Primary Diagnosis IIa: tumor <=2.0 cm, regional lymph node | 35 participants | 63 participants | 28 participants |
| Stage at Primary Diagnosis IIb: tumor >2.0<5.0cm, regional lymph nodes | 24 participants | 56 participants | 32 participants |
| Stage at Primary Diagnosis IIIa: tumor may be >5.0 cm, regional lymph nodes | 23 participants | 45 participants | 22 participants |
| Stage at Primary Diagnosis IIIb: tumor extending to chest wall or skin | 0 participants | 0 participants | 0 participants |
| Stage at Primary Diagnosis IIIc: tumor with extensive lymph node involvement | 9 participants | 15 participants | 6 participants |
| Stage at Primary Diagnosis I: tumor <=2.0, lymph nodes clear, no metastasis | 7 participants | 17 participants | 10 participants |
| Stage at Primary Diagnosis IV: distant metastasis | 0 participants | 0 participants | 0 participants |
| Stage at Primary Diagnosis unknown | 1 participants | 1 participants | 0 participants |
| Weight | 78.78 kg STANDARD_DEVIATION 19.595 | 78.71 kg STANDARD_DEVIATION 19.528 | 78.63 kg STANDARD_DEVIATION 19.561 |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — |
| other Total, other adverse events | 97 / 98 | 99 / 99 |
| serious Total, serious adverse events | 30 / 98 | 21 / 99 |
Outcome results
Primary
Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy
Toxicities are summarized using the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) terms. Participants with treatment-emergent toxicities with a frequency of \>=20% in any treatment arm, and participants with at least one toxicity are reported. Taxane subsets (ABI-007 subset and Taxol subset treatment arms) summarize participants with treatment-emergent toxicities defined as any AEs that begin or worsen in severity grade after the start of taxane treatment (cycle 5, week 9) through 30 days after the last dose of taxane (week 20) and were ongoing 3 months after chemotherapy (month 7). Entire regiments (AC --\> ABI-007 and AC --\> Taxol treatment arms) summarize participants with treatment-emergent toxicities defined as any AEs that begin or worsen in severity grade after the start of chemotherapy (cycle 1, week 1) through 30 days after the last dose of chemotherapy (week 20) and were ongoing 3 months after chemotherapy (month 7).
Time frame: Month 7
Population: Participants in the Treated Population for whom safety data was available 3 months post-chemotherapy
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Endocrine: Hot Flashes/Flushes | 12 participants |
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Dermatology/Skin: Hair Loss/Alopecia (Scalp+Body) | 2 participants |
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Pain: Arthralgia | 7 participants |
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Cardiac General: Hypertension | 4 participants |
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | At least 1 AE at 3 Months | 65 participants |
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Constitutional Symptoms: Insomnia | 3 participants |
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Constitutional Symptoms: Fatigue | 16 participants |
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Neurology: Neuropathy: Sensory | 36 participants |
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Dermatology/Skin: Nail Changes | 14 participants |
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Pain: Myalgia | 10 participants |
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Pain: Other - Extremity | 4 participants |
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Hemorrhage/Bleeding: Nasal | 11 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Pain: Myalgia | 20 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Neurology: Neuropathy: Sensory | 50 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Constitutional Symptoms: Fatigue | 46 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Endocrine: Hot Flashes/Flushes | 28 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Cardiac General: Hypertension | 18 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Pain: Arthralgia | 22 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Hemorrhage/Bleeding: Nasal | 19 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Dermatology/Skin: Nail Changes | 22 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | At least 1 AE at 3 Months | 74 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Dermatology/Skin: Hair Loss/Alopecia (Scalp+Body) | 33 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Pain: Other - Extremity | 15 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Constitutional Symptoms: Insomnia | 16 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Hemorrhage/Bleeding: Nasal | 10 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Constitutional Symptoms: Insomnia | 5 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Neurology: Neuropathy: Sensory | 28 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | At least 1 AE at 3 Months | 65 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Pain: Myalgia | 9 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Cardiac General: Hypertension | 7 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Constitutional Symptoms: Fatigue | 10 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Dermatology/Skin: Hair Loss/Alopecia (Scalp+Body) | 1 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Dermatology/Skin: Nail Changes | 5 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Pain: Arthralgia | 8 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Pain: Other - Extremity | 7 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Endocrine: Hot Flashes/Flushes | 5 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Dermatology/Skin: Hair Loss/Alopecia (Scalp+Body) | 17 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Hemorrhage/Bleeding: Nasal | 18 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Constitutional Symptoms: Fatigue | 32 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Constitutional Symptoms: Insomnia | 11 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Dermatology/Skin: Nail Changes | 10 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Neurology: Neuropathy: Sensory | 35 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Pain: Other - Extremity | 22 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | At least 1 AE at 3 Months | 77 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Cardiac General: Hypertension | 25 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Endocrine: Hot Flashes/Flushes | 22 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Pain: Myalgia | 16 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 3 Months Post Chemotherapy | Pain: Arthralgia | 19 participants |
Comparison: Comparison of percentage of participants with at least one taxane-emergent toxicityp-value: 0.641Fisher Exact
Primary
Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy
Toxicities are summarized using the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) terms. Participants with treatment-emergent toxicities with a frequency of \>=20% in any treatment arm, and participants with at least one toxicity are reported. Taxane subsets (ABI-007 subset and Taxol subset treatment arms) summarize participants with treatment-emergent toxicities defined as any AEs that begin or worsen in severity grade after the start of taxane treatment (cycle 5, week 9) through 30 days after the last dose of taxane (week 20) and were ongoing 6 months after chemotherapy (month 10). Entire regiments (AC --\> ABI-007 and AC --\> Taxol treatment arms) summarize participants with treatment-emergent toxicities defined as any AEs that begin or worsen in severity grade after the start of chemotherapy (cycle 1, week 1) through 30 days after the last dose of chemotherapy (week 20) and were ongoing 6 months after chemotherapy (month 10).
Time frame: Month 10
Population: Participants in the Treated Population for whom safety data was available 6 months post-chemotherapy
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Pain: Myalgia | 8 participants |
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Pain: Other - Extremity | 1 participants |
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Constitutional Symptoms: Fatigue | 11 participants |
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Dermatology/Skin: Nail Changes | 8 participants |
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Neurology: Neuropathy: Sensory | 25 participants |
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | At least 1 AE at 6 Months | 49 participants |
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Endocrine: Hot Flashes/Flushes | 7 participants |
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Cardiac General: Hypertension | 4 participants |
| AC --> ABI-007 | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Pain: Arthralgia | 4 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Cardiac General: Hypertension | 12 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | At least 1 AE at 6 Months | 62 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Dermatology/Skin: Nail Changes | 13 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Pain: Myalgia | 17 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Pain: Other - Extremity | 6 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Endocrine: Hot Flashes/Flushes | 23 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Neurology: Neuropathy: Sensory | 42 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Constitutional Symptoms: Fatigue | 32 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Pain: Arthralgia | 17 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | At least 1 AE at 6 Months | 46 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Neurology: Neuropathy: Sensory | 15 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Constitutional Symptoms: Fatigue | 4 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Endocrine: Hot Flashes/Flushes | 3 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Cardiac General: Hypertension | 7 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Pain: Myalgia | 4 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Pain: Other - Extremity | 5 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Dermatology/Skin: Nail Changes | 3 participants |
| Taxol Subset | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Pain: Arthralgia | 3 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Pain: Arthralgia | 13 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Dermatology/Skin: Nail Changes | 6 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Constitutional Symptoms: Fatigue | 18 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Neurology: Neuropathy: Sensory | 19 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Endocrine: Hot Flashes/Flushes | 17 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Cardiac General: Hypertension | 18 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | At least 1 AE at 6 Months | 65 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Pain: Other - Extremity | 14 participants |
| AC --> Taxol | Participants With Treatment-Emergent Toxicities With a Frequency >=20% at 6 Months Post Chemotherapy | Pain: Myalgia | 8 participants |
Comparison: Comparison of percentage of participants with at least one taxane-emergent toxicityp-value: 0.323Fisher Exact
Secondary
Change From Baseline in Percent Left Ventricular Ejection Fraction (% LVEF) at the Final Evaluation
Decreased left ventricular ejection fraction (LVEF) is an indication of cardiotoxicity. Change from baseline measurements to the final evaluation are summarized.
Time frame: up to week 46
Population: Participants in the treated population who had both baseline and one treatment measurement for %LVEF
| Arm | Measure | Value (MEDIAN) | Dispersion |
|---|---|---|---|
| AC --> ABI-007 | Change From Baseline in Percent Left Ventricular Ejection Fraction (% LVEF) at the Final Evaluation | -1.0 percentage of healthy LVEF | Full Range 7.4 |
| AC --> Taxol | Change From Baseline in Percent Left Ventricular Ejection Fraction (% LVEF) at the Final Evaluation | -1.0 percentage of healthy LVEF | Full Range 93.4 |
Secondary
Mean Taxane Dose Intensity Per Week
Cumulative taxane (ABI-007 or Taxol) dose divided by the number of weeks on taxane treatment.
Time frame: approximately week 9-16
Population: Participants in the treated population who received at least 1 dose of taxane.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| AC --> ABI-007 | Mean Taxane Dose Intensity Per Week | 118.82 mg/m^2/week | Standard Deviation 24.983 |
| AC --> Taxol | Mean Taxane Dose Intensity Per Week | 82.60 mg/m^2/week | Standard Deviation 12.44 |
Secondary
Myelosuppression During Taxane Dosing Cycles
Myelosuppression represented by neutropenia (low absolute neutrophil counts (ANC)) with severity grades according to Common Terminology Criteria for Adverse Events v3.0 (CTCAE). * Grade 1 = \<lower limit of normal (LLN)-1.5\*10\^9/L * Grade 2 = \<1.5 - 1.0\*10\^9/L * Grade 3 = \<1.0 - 0.5\*10\^9/L * Grade 4 = \<0.5\*10\^9/L Values are reported across all severity grades without assessment of relationship to taxane treatment, and also by relation to taxane treatment as reported by investigators.
Time frame: Weeks 9-16
Population: Participants in the treated population who received at least 1 dose of taxane and had laboratory values.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| AC --> ABI-007 | Myelosuppression During Taxane Dosing Cycles | ANC (grades 1-4) | 58 participants |
| AC --> ABI-007 | Myelosuppression During Taxane Dosing Cycles | Taxane-related, grades 1-4 | 11 participants |
| AC --> ABI-007 | Myelosuppression During Taxane Dosing Cycles | Taxane-related, grades 3-4 | 6 participants |
| AC --> Taxol | Myelosuppression During Taxane Dosing Cycles | Taxane-related, grades 3-4 | 5 participants |
| AC --> Taxol | Myelosuppression During Taxane Dosing Cycles | ANC (grades 1-4) | 43 participants |
| AC --> Taxol | Myelosuppression During Taxane Dosing Cycles | Taxane-related, grades 1-4 | 8 participants |
Secondary
Percent of Protocol Taxane Dose
Percent of the protocol-defined taxane (ABI-007 or Taxol) dose that was actually taken by study participants.
Time frame: approximately week 9-16
Population: Participants in the treated population who received at least 1 dose of taxane.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| AC --> ABI-007 | Percent of Protocol Taxane Dose | 91.40 percentage of protocol-defined taxane | Standard Deviation 19.218 |
| AC --> Taxol | Percent of Protocol Taxane Dose | 94.40 percentage of protocol-defined taxane | Standard Deviation 14.217 |
Secondary
Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles)
Summary of the most severe grades using the National Cancer Institute's Common Terminology Criteria for Adverse Events v3.0 (CTCAE) for the following liver and renal function tests. Grade 0 = within normal range for all measurements. Alkaline phosphatase, alanine aminotransferase (ALT), aspartate aminotransferase (AST): * Grade 1 = \> upper limit of normal (ULN) - 2.5\*ULN * Grade 2= \>2.5-5.0\*ULN * Grade 3= \>5.0-20.0\*ULN * Grade 4= \>20.0\*ULN Bilirubin: * Grade 1= \>ULN - 1.5\*ULN * Grade 3= \>3.0 - 10.0\*ULN Creatinine: \- Grade 1= \>ULN - 1.5\*ULN
Time frame: Week 1 up to week 50
Population: Treated population with at least one post-treatment laboratory measure.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| AC --> ABI-007 | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | ALT, Grade 1 | 24 participants |
| AC --> ABI-007 | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | AST, grade 3 | 1 participants |
| AC --> ABI-007 | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | Alkaline phosphatase, Grade 1 | 26 participants |
| AC --> ABI-007 | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | Bilirubin, grade 0 | 95 participants |
| AC --> ABI-007 | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | ALT, Grade 2 | 5 participants |
| AC --> ABI-007 | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | Bilirubin, grade 1 | 0 participants |
| AC --> ABI-007 | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | ALT, Grade 0 | 66 participants |
| AC --> ABI-007 | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | Bilirubin, grade 3 | 1 participants |
| AC --> ABI-007 | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | ALT, Grade 4 | 1 participants |
| AC --> ABI-007 | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | Creatinine, grade 0 | 94 participants |
| AC --> ABI-007 | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | Alkaline phosphatase, Grade 2 | 1 participants |
| AC --> ABI-007 | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | Creatinine, grade 1 | 2 participants |
| AC --> ABI-007 | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | AST, grade 0 | 74 participants |
| AC --> ABI-007 | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | AST, grade 1 | 20 participants |
| AC --> ABI-007 | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | AST, grade 2 | 1 participants |
| AC --> ABI-007 | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | Alkaline phosphatase, Grade 0 | 69 participants |
| AC --> Taxol | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | AST, grade 2 | 1 participants |
| AC --> Taxol | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | Alkaline phosphatase, Grade 0 | 70 participants |
| AC --> Taxol | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | Alkaline phosphatase, Grade 1 | 29 participants |
| AC --> Taxol | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | Alkaline phosphatase, Grade 2 | 0 participants |
| AC --> Taxol | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | ALT, Grade 0 | 75 participants |
| AC --> Taxol | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | ALT, Grade 1 | 23 participants |
| AC --> Taxol | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | ALT, Grade 2 | 1 participants |
| AC --> Taxol | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | ALT, Grade 4 | 0 participants |
| AC --> Taxol | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | AST, grade 1 | 17 participants |
| AC --> Taxol | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | AST, grade 3 | 0 participants |
| AC --> Taxol | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | Bilirubin, grade 0 | 98 participants |
| AC --> Taxol | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | Bilirubin, grade 1 | 1 participants |
| AC --> Taxol | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | Bilirubin, grade 3 | 0 participants |
| AC --> Taxol | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | Creatinine, grade 0 | 97 participants |
| AC --> Taxol | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | Creatinine, grade 1 | 2 participants |
| AC --> Taxol | Summary of Participants' Most Severe Grade for Liver and Renal Function Laboratory Adverse Experiences During Study (All Treatment Cycles) | AST, grade 0 | 81 participants |
Secondary
Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays
Counts of participants who * completed the protocol-defined treatment cycles, * had a dose interruption * had a dose reduction * had a dose delay. A dose delay refers to the delay of all interventions in the cycle. Dose modifications are typically caused by clinically significant laboratory abnormalities and /or treatment emergent adverse events/toxicities. Use of pegfilgrastim is included in the summary.
Time frame: up to Week 46
Population: Treated population
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| AC --> ABI-007 | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | One or more dose reduction: Adriamycin | 10 participants |
| AC --> ABI-007 | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | One or more dose interruption: Cytoxan | 3 participants |
| AC --> ABI-007 | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | Received pegfilgrastim for 4 cycles during AC | 95 participants |
| AC --> ABI-007 | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | One or more dose interruption: Taxane | 0 participants |
| AC --> ABI-007 | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | One or more dose reduction: Cytoxan | 9 participants |
| AC --> ABI-007 | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | Completed 18 cycles of bevacizumab | 61 participants |
| AC --> ABI-007 | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | One or more delay in study regimen | 50 participants |
| AC --> ABI-007 | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | One or more dose reduction: Taxane | 12 participants |
| AC --> ABI-007 | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | Discontinued pegfilgrastim during AC cycles | 0 participants |
| AC --> ABI-007 | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | Completed 4 cycles of taxane | 82 participants |
| AC --> ABI-007 | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | One or more dose interruption: Bevacizumab | 0 participants |
| AC --> ABI-007 | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | One or more dose interruption: Adriamycin | 1 participants |
| AC --> ABI-007 | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | Administered pegfilgrastim during taxane cycles | 23 participants |
| AC --> ABI-007 | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | Completed 4 cycles of Adriamycin/Cytoxan (AC) | 95 participants |
| AC --> Taxol | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | Administered pegfilgrastim during taxane cycles | 13 participants |
| AC --> Taxol | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | Completed 4 cycles of Adriamycin/Cytoxan (AC) | 95 participants |
| AC --> Taxol | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | Completed 4 cycles of taxane | 84 participants |
| AC --> Taxol | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | Completed 18 cycles of bevacizumab | 61 participants |
| AC --> Taxol | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | One or more dose reduction: Adriamycin | 6 participants |
| AC --> Taxol | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | One or more dose reduction: Cytoxan | 5 participants |
| AC --> Taxol | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | One or more dose reduction: Taxane | 16 participants |
| AC --> Taxol | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | One or more dose interruption: Adriamycin | 0 participants |
| AC --> Taxol | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | One or more dose interruption: Cytoxan | 1 participants |
| AC --> Taxol | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | One or more dose interruption: Taxane | 3 participants |
| AC --> Taxol | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | One or more dose interruption: Bevacizumab | 2 participants |
| AC --> Taxol | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | One or more delay in study regimen | 48 participants |
| AC --> Taxol | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | Received pegfilgrastim for 4 cycles during AC | 94 participants |
| AC --> Taxol | Summary of Participant Treatment Exposure, Dose Interruptions, Dose Reductions, and Dose Delays | Discontinued pegfilgrastim during AC cycles | 0 participants |
Secondary
The Cumulative Dose of Taxane Delivered During Study
The cumulative dose of taxane (Taxol or ABI-007) taken during the study (cycles 4-8 which is approximately weeks 9-16).
Time frame: approximately week 9-16
Population: Participants in the treated population who received at least 1 dose of taxane.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| AC --> ABI-007 | The Cumulative Dose of Taxane Delivered During Study | 950.5 mg/m^2 | Standard Deviation 199.86 |
| AC --> Taxol | The Cumulative Dose of Taxane Delivered During Study | 660.8 mg/m^2 | Standard Deviation 99.52 |