Efficacy and Safety of Cabazitaxel Versus Weekly Paclitaxel as Neo-adjuvant Treatment in Patients With Triple Negative or Luminal B/HER2 Normal BC (GENEVIEVE)
The recruitment status of this study is unknown because the information has not been verified recently.
Verified May 2013 by German Breast Group.
Recruitment status was Recruiting
Information provided by (Responsible Party):
German Breast Group
First received: January 25, 2013
Last updated: July 16, 2014
Last verified: May 2013
Cabazitaxel is a new taxoid which promotes the tubulin assembly in vitro and stabilizes microtubules against cold-induced depolymerization as efficiently as docetaxel and was selected for development based on a better antiproliferative activity on resistant cell lines than docetaxel. It has shown superior survival against mitoxantrone (MTX) plus prednisone in docetaxel pre-treated hormone refractory metastatic prostate cancer patients leading to registration of the compound. It showed a favorable toxicity profile with an interestingly low rate of alopecia. In the Genevieve study it will be compared against weekly paclitaxel which is currently most widely used treatment of breast cancer patients. A head-to-head comparison in the neoadjuvant setting will allow a rapid and precise comparison of efficacy and tolerability of cabacitaxel versus paclitaxel to decide in how far further development of this taxoid in breast cancer is reasonable.
Primary Breast Cancer
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
||Randomized, Open-label, Phase II Study Comparing the Efficacy and the Safety of Cabazitaxel Versus Weekly Paclitaxel Given as Neo-adjuvant Treatment in Patients With Operable Triple Negative or Luminal B/HER2 Normal Breast Cancer (GENEVIEVE)
Primary Outcome Measures:
- pathologic complete response (pCR) rate [ Time Frame: 15 months ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- pathologic complete response (pCR) rate separately for subpopulations [ Time Frame: 15 months ] [ Designated as safety issue: No ]
pathologic complete response (pCR) rate separately for stratified subpopulations
- Objective response rate (ORR) [ Time Frame: 15 months ] [ Designated as safety issue: No ]
- pCR rate defined as ypT0 ypN0 [ Time Frame: 15 months ] [ Designated as safety issue: No ]
- pCR rate defined as ypT0/is ypN0 [ Time Frame: 15 months ] [ Designated as safety issue: No ]
- pCR rate in the axillary lymph nodes (ypN0) [ Time Frame: 15 months ] [ Designated as safety issue: No ]
- pCR rate in patients with a clinical complete response (cCR) [ Time Frame: 15 months ] [ Designated as safety issue: No ]
To determine the pCR rate in patients with a clinical complete response (cCR) and a negative core biopsy before surgery
- local recurrence free survival (LRFS) in patients with a clinical complete response (cCR) [ Time Frame: 15 months ] [ Designated as safety issue: No ]
To determine the local recurrence free survival (LRFS) in patients with a clinical complete response (cCR) and a negative core biopsy before surgery
- Breast conservation surgery rate [ Time Frame: 15 months ] [ Designated as safety issue: No ]
- Toxicity [ Time Frame: 15 months ] [ Designated as safety issue: Yes ]
To assess the toxicity (NCI CTCAE V4.03) in both arms.
- Compliance [ Time Frame: 15 months ] [ Designated as safety issue: No ]
To assess compliance in both arms.
- Invasive loco-regional recurrence free survival (LRRFS) [ Time Frame: 15 months ] [ Designated as safety issue: No ]
- Distant-disease-free survival (DDFS) [ Time Frame: 15 months ] [ Designated as safety issue: No ]
- Invasive disease-free survival (IDFS) [ Time Frame: 15 months ] [ Designated as safety issue: No ]
- Overall survival (OS) [ Time Frame: 15 months ] [ Designated as safety issue: No ]
| Estimated Enrollment:
| Study Start Date:
| Estimated Study Completion Date:
| Estimated Primary Completion Date:
||December 2014 (Final data collection date for primary outcome measure)
Cabazitaxel 25 mg/m² i.v. (Day 1) every 3 weeks (cycle) as 1-hour i.v infusion for a total of up to 4 cycles over a maximum total treatment period of 15 weeks before surgery
Active Comparator: Paclitaxel
Paclitaxel 80 mg/m² as 1-hour i.v infusion. Patients will receive weekly (Days 1, 8, 15) paclitaxel administrations for a maximum of 12 infusions for a maximum of 4 cycles over a maximum total treatment period of 15 weeks before surgery (1 cycle = 3 weeks).
Primary Objective To compare the pathologic complete response (pCR) rate in the breast (ypT0/is ypN0/+) in patients with operable Triple Negative or luminal B/HER2 normal breast cancer treated with either cabazitaxel or weekly paclitaxel.
Secondary Objective To assess
- pCR rates per arm separately for the stratified subpopulations.
- Objective response rate (ORR) in the breast according to WHO criteria.
- pCR rate defined as ypT0 ypN0.
- pCR rate defined as ypT0/is ypN0.
- pCR rate in the axillary lymph nodes (ypN0).
- To determine the pCR rate and local recurrence free survival (LRFS) in patients with a clinical complete response (cCR) and a negative core biopsy before surgery.
- Breast conservation surgery rate.
- To assess the toxicity (NCI CTCAE V4.03) and compliance in both arms.
- Invasive loco-regional recurrence free survival (LRRFS), distant-disease-free survival (DDFS), invasive disease-free survival (IDFS), and overall survival (OS).
- To explore the biomarkers and profiles potentially predicting response to treatment.
|Ages Eligible for Study:
||18 Years and older
|Genders Eligible for Study:
|Accepts Healthy Volunteers:
- Written informed consent for all study according to local regulatory requirements prior to beginning specific protocol procedures.
- Complete baseline documentation must be sent to GBG Forschungs GmbH.
- Unilateral or bilateral primary carcinoma of the breast, confirmed histologically by core biopsy. Fine-needle aspiration alone is not sufficient. Incisional biopsy is not allowed. In case of bilateral cancer, the investigator has to decide prospectively which side will be evaluated for the primary endpoint.
- Tumor lesion in the breast with a palpable size of >= 2 cm or a sonographical size of >= 1 cm in maximum diameter. The lesion has to be measurable in two dimensions, preferably by sonography.
- Patients must be in the following stages of disease: cT3 or cT2 or cT1c and cN+ or cT1c and pNSLN+.
- In patients with multifocal or multicentric breast cancer, the largest lesion should be evaluated.
- Centrally confirmed triple negative or luminal B/HER2-normal subtype. ER- and PgR-negative defined as <1% stained cells. HER-2 negative defined as IHC 0+, 1+ or IHC 2+ and FISH/SISH/CISH (ratio <2.0) negative. Luminal B defined as ER and/or PgR + and > 14% Ki-67 stained cells. The formalin-fixed, paraffin-embedded (FFPE) breast tissue block from the diagnostic core biopsy has therefore to be sent to the Dept. of Pathology at the Charité, Berlin prior to randomization.
- Age >= 18 years.
- Eastern Cooperative Oncology Group (ECOG) Performance Status: 0 or 1 (see Appendix A).
- Laboratory requirements: Hemoglobin > 9.0 g/dL, Absolute neutrophil count > 1.5 x 109/L, Platelet count > 100 x 109/L, AST/SGOT and/or ALT/SGPT < 2.5 x ULN; Total bilirubin < 1.0 x ULN, Serum creatinine < 1.5 x ULN. If creatinine 1.0 - 1.5 x ULN, creatinine clearance will be calculated according to CKD-EPI formula and patients with creatinine clearance < 60 mL/min should be excluded (see Appendix 2 for formula).
- Negative pregnancy test (urine or serum) within 14 days prior to randomization for all women of childbearing potential.
- Complete staging work-up within 3 months prior to randomization. All patients must have bilateral mammography, breast ultrasound (<= 21 days), breast MRI (optional), chest X-ray (PA and lateral), abdominal ultrasound or CT scan or MRI, and bone scan done. In case of positive bone scan, bone X-ray is mandatory. Other tests may be performed as clinically indicated.
- Patients must be available and compliant for central diagnostics, treatment and follow-up.
- Any prior treatment for primary breast cancer including radiation therapy
- History of ipsi/ or contra-lateral invasive breast cancer
- Locally advanced disease including N3 and metastatic disease
- Patients in the following stages of disease are not allowed: cT4
- Prior malignancy without being disease-free for more than 5 years (except carcinoma in situ of the cervix or other in situ cancer (e.g. bladder cancer) and adequately treated basal cell carcinoma of the skin.
- Clinically significant (i.e. active) cardiovascular disease, including cerebrovascular accident (≤6 months before enrolment), myocardial infarction, arterial thrombotic events (≤6 months before enrolment), unstable angina pectoris, New York Heart Association (NYHA) ≥ grade 2 congestive heart failure and/or hypertension, serious cardiac arrhythmia requiring medication during the study and that might interfere with regularity of the study treatment, or not controlled by medication
- Any severe acute or chronic medical condition which could impair the ability of the patient to participate to the study or to comply with the study procedures or interfere with interpretation of study results (such as significant neurological or psychiatric disorders including psychotic disorders, dementia or seizures).
- Active infection.
- Sex hormones. Prior treatment must be stopped before study entry.
- Inability and unwillingness to comply with study visits, treatment, testing, and to comply with the protocol.
- Administration of any live virus vaccine within 8 weeks preceding study entry.
- Use of any investigational agent within 30 days of administration of the first dose of study drug or concurrent treatment on another clinical trial
- Requirement for radiation therapy concurrent with study anticancer treatment. Patients who require breast or chest wall radiation therapy after surgery are eligible
- Pregnancy or breastfeeding women
- Patients with childbearing potential who do not agree to use accepted and effective method of contraception (barrier methods, intrauterine contraceptive devices, sterilization) during the study treatment period and following a period of 6 months after the last study drug administration.
- History of hypersensitivity (grade ≥ 3) to polysorbate 80 or any study drugs or excipients
- Concurrent or planned treatment with potent strong inhibitors or strong inducers of cytochrome P450 3A4/5 (a two-week wash-out period is necessary for patients who are already on these treatments) (see Appendix 3)
- Contraindications to the use of corticosteroid treatment
- Symptomatic peripheral neuropathy grade ≥ 2 (National Cancer Institute Common Terminology Criteria [NCI CTCAE] v.4.03).
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Please refer to this study by its ClinicalTrials.gov identifier: NCT01779479
|Düsseldorf, Germany, 40235 |
|Contact: Mahdi Rezai, Rezai +49-211-69922 ext 200 firstname.lastname@example.org |
|Principal Investigator: Mahdi Rezai, Dr. med. |
German Breast Group
||Gunter von Minckwitz, Prof. Dr.
No publications provided
||German Breast Group
History of Changes
|Other Study ID Numbers:
||GBG 74, 2012-003330-16
|Study First Received:
||January 25, 2013
||July 16, 2014
||Germany: Federal Institute for Drugs and Medical Devices
Keywords provided by German Breast Group:
German Breast Group
GBG Forschungs GmbH
Primary Breast Cancer
Additional relevant MeSH terms:
ClinicalTrials.gov processed this record on December 01, 2015
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