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Completed

NCT Number: NCT01190345

Anti Cancer Stem Cell Activity of Pre-operative Bevacizumab and 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.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

Jean-Marc EXTRA, MD, Marseille, France

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Bevacizumab

Drug

Patients receive on day 1 of each cycle : bevacizumab 15 mg/kg (8 injections in total).

Other names: avastin

no bevacizumab

Drug

no bevacizumab

Primary outcomes

  1. Measure of the anti-cancer stem cell activity

    Time frame: 4 months

    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

Secondary outcomes

  1. Evaluation of the safety of the treatment

    Time frame: 8 months

    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

  2. Evaluation of the disease-free survival, recurrence-free survival and overall survival

    Time frame: 5 years

    The disease-free survival, recurrence-free survival and overall survival are calculated from the inclusion to the time of the event

  3. Evaluation of the pathological complete response rate

    Time frame: 8 months

    Evaluation of the pathological complete response rate according to the classification of Sataloff

Sponsors and collaborators

Lead sponsor

Institut Paoli-Calmettes

Other

Registry information

Official study title

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

Acronym: AVASTEM

Important dates

Study start
2010
Primary completion
2012
Study completion
2017
First posted
Aug 27, 2010
Registry last updated
Aug 13, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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