Squamous Cell Carcinoma of the Penis Clinical Trial
— MRI-PETOfficial title:
Characterising Metastatic Penile Cancer Using Molecular Imaging - Hybrid MRI-PET [MRI-PET]
The presence of metastatic disease in the lymph nodes within the groin is the most important
factor in predicting the long-term outcome for patients diagnosed with penile cancer.
In the majority of patients diagnosed with penile cancer obvious abnormalities cannot be felt
in the groin even though the cancer may have already spread to the lymph nodes in the groin.
In these patients, a procedure called Dynamic Sentinel Lymph Node Biopsy (DSLB) is required
to determine if the cancer has spread to the lymph nodes in the groin. In DSLB a radioactive
substance is injected at the site of the penile cancer and then travels to the lymph nodes in
the groin which are then biopsied. This procedure requires a general anaesthetic and an
in-patient hospital stay.
In approximately 20% of patients with penile cancer obvious abnormalities can be felt in the
lymph nodes in the groin. However, any abnormality detected may not necessarily be due to
metastatic disease. In order to confirm if metastatic disease is present in the lymph nodes
of these patients a biopsy is also required. However in these patients the lymph nodes are
detected and biopsied using an ultrasound scan rather than by passing a radioactive substance
into the body.
MRI-PET is a new procedure which combines conventional MRI (Magnetic Resonance Imaging) and
PET (Positron Emission Tomography) scans into one scan. MRI - PET scans create very clear
pictures of internal body structures. MRI-PET is a non-invasive procedure which can be
performed on an out-patient basis.
The accuracy of MRI-PET in detecting metastatic penile cancer is not known. The main purpose
of this study is to establish the effectiveness of MRI-PET compared to DSLB and ultrasound
guided biopsy in detecting the presence of metastatic disease in the lymph nodes of patients
with penile cancer. If effective, MRI-PET could replace the invasive procedures currently
required for detection of metastatic penile cancer.
Status | Recruiting |
Enrollment | 107 |
Est. completion date | March 2018 |
Est. primary completion date | March 2018 |
Accepts healthy volunteers | No |
Gender | Male |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Squamous cell carcinoma of the penis. - Men aged >= 18 years. - Willing and able to give written informed consent prior to study entry. - Patients must be sterile or agree to use adequate contraception during the study period. Exclusion Criteria: - Any co-existing medical condition that in the Investigator's judgement will substantially increase the risk associated with the patient's participation in the study. - Any known contraindication to MRI such as ferrous metal implants, electrical implants (e.g. cochlear implants, cardiac pacemaker), or history of injury involving metal fragments. - Any known contraindication to PET scans. - Any known allergy to FDG (18F-2-fluoro-2-deoxy-D-glucose fluorodeoxyglucose). - Uncontrolled diabetes. - Inability to comply with the study procedures. - Medical or psychiatric illness, which makes the patient unsuitable or unable to give informed consent. |
Country | Name | City | State |
---|---|---|---|
United Kingdom | University College London Hospitals | London |
Lead Sponsor | Collaborator |
---|---|
Queen Mary University of London |
United Kingdom,
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* Note: There are 16 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Evaluating the clinical validity (sensitivity, specificity, negative and positive predictive values) of whole-body MRI-PET to detect or exclude micrometastatic disease in inguinal lymph nodes. | Evaluating the clinical validity (sensitivity, specificity, negative and positive predictive values) of whole-body MRI-PET imaging to detect or exclude micrometastatic disease in inguinal lymph nodes in patients diagnosed with squamous cell carcinoma of the penis using dynamic sentinel lymph node biopsy as the reference standard for clinically impalpable inguinal lymph nodes and ultrasound guided fine needle aspiration/ excisional biopsy as the reference standard in patients with clinically palpable inguinal lymph nodes. | 3 years |
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