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Completed

NCT Number: NCT02583568

Fluorescence Guided Surgery in Breast Cancer

A need for further investigation for fluorescence image-guided surgery in breast conserving surgery (BCS) has arisen following the results obtained from a phase I feasibility breast cancer trial (BIRDYE study: ABR NL 37479.042011). The aim of this study is to define the optimal dose of the fluorescent tracer Bevacizumab-IRDye800CW for intraoperative delineation of breast cancer tissue using the improved and optimized fluorescent tracer and camera system.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

University Medical Center Groningen

Groningen, Provincie Groningen, 9713 GZ, Netherlands

Who can participate

Healthy volunteers accepted: No

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

Main Inclusion Criteria:

  • Females aged ≥ 18 years.
  • Confirmed diagnosis of breast cancer by means of histology or cytology and eligible for breast cancer surgery.
  • Tumor size ≥ 5 mm (0, 5 cm) diameter according to anatomical imaging data.
  • WHO performance score 0-2.
  • Life expectancy greater than 12 weeks
  • Written informed consent has been obtained
  • In the Investigator's opinion, patient is able and willing to comply with all trial requirements.

For female subjects who are of childbearing potential, are premenopausal with intact reproductive organs or are less than 2 years post-menopausal:

  • A negative serum pregnancy test prior to receiving the second generation tracer
  • Willing to ensure that she or her partner uses effective contraception during the trial and for 3 months thereafter.

Main Exclusion Criteria:

  • Medical or psychiatric conditions that compromise the patient's ability to give informed consent
  • Breast prosthesis in the target breast
  • History of infusion reactions to Bevacizumab or other monoclonal antibody therapies
  • Concurrent anticancer therapy (chemotherapy, radiotherapy, vaccines, immunotherapy) delivered within the last 6 weeks prior to the start of the treatment
  • Significant renal or hepatic impairment.
  • Inadequately controlled hypertension with or without current antihypertensive medications.
  • History of myocardial infarction, transient ischemic attack, cerebro vascular accident, pulmonary embolism, uncontrolled congestive heart failure (CHF), significant liver disease, unstable angina within 6 months prior to enrollment.
  • Patients receiving anticoagulant therapy with vitamin K antagonists.
  • Patients receiving Class IA (e.g. Quinidine) or Class III (e.g. Dofetilide, Amiodarone, Sotalol) antiarrhythmic agents.
  • Evidence of QT prolongation on pre-treatment ECG (Males >440 ms, Females >450 ms).
  • Magnesium, potassium and calcium levels below lower normal limit which is regarded clinically relevant with regards to study participation.

Treatment and study plan

Bevacizumab-800CW

Drug

three days prior to surgery bevacizumab-800CW will be administered

Other names: Bevacizumab-IRDye800CW

Primary outcomes

  1. Tumor-to-background ratio

    Time frame: day 3

Secondary outcomes

  1. Number of participants with treatment-related adverse events

    Time frame: up to two weeks

Sponsors and collaborators

Lead sponsor

University Medical Center Groningen

Other

Collaborators

  • Martini Hospital Groningen

Registry information

Official study title

Phase II, Open-Label Study to Evaluate Safety and Explore Efficacy of Escalating Doses of Bevacizumab-IRDye800CW as an Optical Imaging Agent to Detect Cancer Tissue Delineation During Tumor Resection Surgery in Patients With Breast Cancer

Acronym: MARGIN

Important dates

Study start
2015
Primary completion
2017
Study completion
2017
First posted
Oct 22, 2015
Registry last updated
Feb 13, 2017

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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