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Nano MRI on 7 Tesla in Rectal and Breast Cancer

R

Radboud University Medical Center

Status and phase

Unknown
Phase 3

Conditions

Breast Neoplasms
Rectal Neoplasms

Treatments

Device: 3 Tesla MRI
Device: 7 Tesla MRI
Drug: ferumoxtran-10

Study type

Interventional

Funder types

Other

Identifiers

NCT02751606
7TNANO1

Details and patient eligibility

About

This study evaluates the diagnostic accuracy of an USPIO contrast agent (ferumoxtran-10) in combination with 7 Tesla MRI to detect lymph node metastases in rectal and breast cancer.

Full description

The Presence of lymph node metastases in cancer is a key factor for determining prognosis and forming an adequate treatment plan. Determining lymph node status, however, is a challenge. Ferumoxtran-10, an ultrasmall superparamagnetic iron oxide (USPIO) particle has proven to be a valuable contrast agent for detecting lymph node metastases using magnetic resonance imaging (MRI) in various types of cancer (also called nano-MRI). For small lymph node metastases (<5mm) the diagnostic accuracy of this technique does, however, drop substantially. Most of the studies that have been performed with these particles used a 1.5 Tesla or 3 Tesla MRI scanner. The investigators would like to increase the resolution of nano-MRI by using a 7 Tesla scanner, such that the investigators can increase the sensitivity of this technique for small lymph nodes. With this study the investigators would like to validate the results of this technique with pathology in rectal and breast cancer. In these cancer types many patients undergo a surgical lymph node dissection by bulk excision of tissue including the nodes, enabling a node-to-node comparison between MRI and pathology to validate our nano-MRI results . If successful this technique would form a non-invasive alternative to the current lymph node staging techniques such as surgery. Additionally (if metastatic nodes are present), it could complement image guided focal therapies on lymph node metastases such as radiotherapy.

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

General criteria:

  • Age > 18 years

Inclusion criteria rectal cancer patients:

  • Patients with recently histologically proven rectal cancer, who are planned to undergo a total mesorectal excision without neo-adjuvant radiotherapy.

Inclusion criteria breast cancer patients:

  • Patients with recently histologically proven breast cancer (Stage II), who are planned for surgery with sentinel node procedure, but will receive no neo-adjuvant therapy or will undergo an axillary lymph node dissection without prior sentinel node procedure and will receive no neo-adjuvant therapy.

Exclusion criteria

General exclusion criteria:

  • BMI > 30 kg/m2

  • Pregnancy

  • Karnofsky score <= 70

  • Contraindications for 7T MRI:

    • Epilepsy
    • Inability to provide informed consent
    • Metal implants that are not compatible with 7 Tesla MRI
  • Contraindications to USPIO based contrast agents:

    • prior allergic reaction to ferumoxtran-10 or any other iron preparation
    • prior allergic reaction contributed to dextran or other polysaccharide, in any preparation
    • prior allergic reaction to contrast media of any type
    • hereditary hemochromatosis, thalassemia, sickle cell anemia;

Exclusion criteria for rectal cancer:

  • Inflammatory diseases of the abdomen (such as Crohn's disease)
  • Previous abdominal surgery or radiotherapy

Exclusion criteria for breast cancer:

  • Prior radiotherapy or surgery to axillae

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Breast and rectal cancer
Experimental group
Description:
Subjects will receive intravenous dose of ferumoxtran-10. 24-36 hours later a 7 Tesla MRI scan will be performed, to detect lymph node metastases. In rectal cancer patients the mesorectum will be imaged and for breast cancer patients this will be performed in the ipsilateral axilla. Subjects will also undergo a 3 Tesla MRI scan as a comparison to the 7 Tesla MRI scan.
Treatment:
Device: 3 Tesla MRI
Drug: ferumoxtran-10
Device: 7 Tesla MRI

Trial contacts and locations

1

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Central trial contact

Bart Philips, MD

Data sourced from clinicaltrials.gov

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