Know Cancer

or
forgot password

A Prospective Cohort Study to Evaluate the Impact of Preoperative Breast Magnetic Resonance Imaging (MRI) on Surgical Decision-Making in Young Patients With Breast Cancer


N/A
N/A
50 Years
Open (Enrolling)
Female
Breast Cancer, Magnetic Resonance Imaging, Preoperative MRI

Thank you

Trial Information

A Prospective Cohort Study to Evaluate the Impact of Preoperative Breast Magnetic Resonance Imaging (MRI) on Surgical Decision-Making in Young Patients With Breast Cancer


Inclusion Criteria:

- female aged ≤ 50

- histologically proven invasive breast cancer

Exclusion Criteria:

- Is not considered a surgical candidate

- Has had prior breast cancer surgery or an excisional biopsy of the newly diagnosed
lesion

- Has a contraindication to undergoing breast MRI

- Has inflammatory breast cancer according to the standard clinical definition

- Has locally advanced breast cancer according to the standard clinical definition

- Patient is pregnant

- Has a psychiatric or addictive disorder that would preclude obtaining informed consent
or adherence to the protocol


Inclusion Criteria:



- Female aged <= 50 years

- Histological proof of invasive breast cancer via fine needle aspiration or core
needle biopsy

- Premenopausal

Exclusion Criteria:

- Patient not considered an appropriate surgical candidate; i.e., patient is not well
enough to have breast cancer surgery

- Patient has had prior breast cancer surgery or an excisional biopsy of the newly
diagnosed cancer

- Patient has a contraindication to undergoing breast MRI (i.e., pacemaker,
neurodefibrillator, metallic foreign bodies, etc.)

- Patient has inflammatory breast cancer according to the standard clinical definition.
This is a type of breast cancer in which there is evidence of erythema and/or edema.
The skin of the breast may also have changes of peau d'orange.

- Patient has locally advanced breast cancer according to the standard clinical
definition.

- Patient is pregnant

- Patient has a psychiatric or addictive disorder that would preclude them from
obtaining informed consent.

Type of Study:

Interventional

Study Design:

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Outcome Measure:

Does pre-operative magnetic resonance imaging (MRI) effect surgical management in young women with breast cancer

Outcome Time Frame:

3 months

Safety Issue:

No

Principal Investigator

Nicole Hodgson, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Juravinski Cancer Centre

Authority:

Canada: Health Canada

Study ID:

MRI REB 07-458

NCT ID:

NCT00801476

Start Date:

April 2008

Completion Date:

May 2010

Related Keywords:

  • Breast Cancer
  • Magnetic Resonance Imaging
  • Preoperative MRI
  • Breast Cancer
  • Magnetic Resonance Imaging
  • Preoperative MRI
  • Breast Neoplasms

Name

Location