Anti Cancer Stem Cell Activity of Pre-operative Bevacizumab and Chemotherapy in Breast Cancer (AVASTEM)

Phase II" Proof of Concept " Trial Evaluating Anti Cancer Stem Cell Activity of Pre-operative Bevacizumab in Combination With Chemotherapy in Breast Cancer

The purpose of this study is to evaluate anti-cancer stem cell (CSC) activity (measured by the amount of Aldehyde dehydrogenase 1/ALDH1+ cells before and after treatment) of pre-operative bevacizumab in combination with conventional chemotherapy in breast cancer receiving neo-adjuvant treatment, compared to a control arm receiving chemotherapy alone.

Study Overview

• Status: Completed
• Conditions: Breast Cancer
• Intervention / Treatment: Drug: bevacizumab; Drug: no bevacizumab

• Study Type: Interventional
• Enrollment (Anticipated): 75
• Phase: Phase 2

Contacts and Locations

Study Locations

• France
  • Marseille, France, 13009
    • Jean-Marc EXTRA, MD
  • Paris, France
    • Jean-Yves PIERGA
  • Reims, France
    • Hervé CURE

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: Female

Description

Inclusion Criteria:

• Women older than 18 ys
• Primary breast cancer treated in the neoadjuvant setting (synchronous metastatic disease are eligible)
• Primary breast tumor accessible to initial biopsy
• White Blood Count > 3.000/µl and Absolute neutrophil count ≥ 1.500/µl AND platelets ≥ 100 x 109/L AND Hemoglobin ≥ 9 g/dL, Serum creatinine ≤ 150µm/l• Urine dipstick for proteinuria < 2+. Patients discovered to have ≥ 2+ proteinuria on dipstick urinalysis at baseline should undergo a 24 hour urine collection and must demonstrate ≤ 1 g of protein in 24 hours, Total bilirubin ≤ 1.5 ULN and ASAT < 2.5 ULN AND ALAT < 1.5 ULN (2.5 if liver metastasis), Adequate coagulation function: International normalized ratio (INR) ≤ 1.5 and TCA ≤ 1.5 x ULN
• Left ventricular ejection fraction (LVEF) ≥ 55% (isotopic or
• ultrasound methods)
• Karnofsky Index > 1 ; Performance status 0 to 1
• Patients must have signed a written informed consent form prior to any study specific screening procedures
• Patient affiliated to the national "Social Security" regimen or beneficiary of this regimen.

Exclusion Criteria:

• Previous history of cancer (other than curatively treated basal and squamous cell carcinoma of the skin and/or in-situ carcinoma of the cervix) relapsing within the 5 years before study entry
• Known contra-indication to anticancer compounds used
• Uncontrolled hypertension (systolic >150 mmHg and/or diastolic >100 mmHg) or history of hypertensive encephalopathy
• History of inherited diathesis or recent thrombotic events
• Non-healing wound, active peptic ulcer or bone fracture.
• Major surgery or significant traumatic injury within 28 days prior to study treatment start
• History of abdominal fistula, trachea-oesophageal fistula or urinary fistula
• Use of Non Steroid Anti Inflammatory or full dose anticoagulants or antiaggregation treatments within 10 days
• Pregnancy and breast feeding, premenopausal patient and no effective contraception
• Brain metastasis.
• Any unstable severe disease such as : uncontrolled cardiac or vascular disease, uncontrolled hemorrhagy, uncontrolled neuropsychiatric disorders, including dementia, uncontrolled infection or any severe disorders that may preclude study participation
• Patient considered geographically, socially or psychologically unable to comply with the treatment and the required medical follow-up.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: WITH bevacizumab; bevacizumab 15 mg/kg on day 1 of each cycle : 4 cycles of 5-fluorouracil 500 mg/m² IV + epirubicin 100 mg/m² IV + cyclophosphamide 500 mg/m² IV (FEC100) every 21 days and 4 cycles of docetaxel 100 mg/m² IV every 21 days. Patients with HER2+ disease will receive trastuzumab (8 mg/kg (IV then 6 mg/kg, every 21 days), which will be started with docetaxel and administered for a total duration of 54 weeks, 18 injections.	Drug: bevacizumab; Patients receive on day 1 of each cycle : bevacizumab 15 mg/kg (8 injections in total).; Other Names: avastin
Active Comparator: without bevacizumab; 4 cycles 5-fluorouracil 500 mg/m² IV + epirubicin 100 mg/m² IV + cyclophosphamide 500 mg/m² IV of (FEC100) every 21 days and 4 cycles of docetaxel 100 mg/m² IV every 21 days. Patients with HER2+ disease will receive trastuzumab (8 mg/kg (IV then 6 mg/kg, every 21 days), which will be started with docetaxel and administered for a total duration of 54 weeks, 18 injections.	Drug: no bevacizumab; no bevacizumab

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Measure of the anti-cancer stem cell activity	The anti-cancer stem cell (CSC) activity is measured by the amount of Aldehyde dehydrogenase 1/ALDH1+ cells after 4 cycles of treatment compared to the amount before treatment	4 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Evaluation of the safety of the treatment	Evaluation of the safety of the treatment at each cycle, estimated by the number of patients with clinical and biological adverse events coded according to the CTCAE	8 months
Evaluation of the disease-free survival, recurrence-free survival and overall survival	The disease-free survival, recurrence-free survival and overall survival are calculated from the inclusion to the time of the event	5 years
Evaluation of the pathological complete response rate	Evaluation of the pathological complete response rate according to the classification of Sataloff	8 months

Collaborators and Investigators

• Sponsor: Institut Paoli-Calmettes
• Investigators: Principal Investigator: Jean-Marc EXTRA, MD, Institut Paoli-Calmettes

Publications and helpful links

Helpful Links

• institut Paoli-Calmettes web site

Study record dates

Study Major Dates

• Study Start (Actual): May 1, 2010
• Primary Completion (Actual): July 24, 2012
• Study Completion (Actual): October 6, 2017

Study Registration Dates

• First Submitted: August 24, 2010
• First Submitted That Met QC Criteria: August 26, 2010
• First Posted (Estimate): August 27, 2010

Study Record Updates

• Last Update Posted (Actual): August 13, 2018
• Last Update Submitted That Met QC Criteria: August 10, 2018
• Last Verified: August 1, 2018

More Information

Terms related to this study

• Keywords: breast cancer
• Additional Relevant MeSH Terms: Skin Diseases; Neoplasms; Neoplasms by Site; Breast Diseases; Breast Neoplasms; Physiological Effects of Drugs; Antineoplastic Agents; Antineoplastic Agents, Immunological; Angiogenesis Inhibitors; Angiogenesis Modulating Agents; Growth Substances; Growth Inhibitors; Bevacizumab
• Other Study ID Numbers: AVASTEM/IPC 2009-001