The Role of Functional Magnetic Resonance Imaging in Preoperative Assessment of Primary Penile Carcinoma

ConditionPenile Cancer
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexMale
AgeNot listed
SponsorOslo University Hospital

About this trial

The proposed project is intended as a prospective study that includes 60 patients with newly diagnosed penile squamous cell carcinoma (SCC) referred to Oslo University Hospital (OUH), Radiumhospitalet, for surgery, primarily organ-sparing surgery (OSS).

OSS may improve not only quality of life, but also quality of sexual function. However, there is a potential for increased risk of local recurrence after OSS compared to the amputation of the penis. Appropriate preoperative staging, including multi-parametric magnetic resonance imaging (mpMRI), can substantially improve selection of patients and decrease the recurrence rate after surgery.

MpMRI without artificial erection is promising diagnostic tool that is poised to be all-in-one solution for staging and preoperative assessment of primary penile cancer, especially prior to OSS. The method is non-invasive and thus comfortable to perform for most of the patients. Novel MRI techniques are not incorporated into current clinical recommendations, and the potential of new, functional sequences has not been evaluated before. The accuracy of functional, non-erectile mpMRI for detecting and staging of primary penile cancer is not known. Thus, the main purpose of this study is to assess the diagnostic value of this method for preoperative assessment of penile cancer.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

newly diagnosed penile squamous cell carcinoma (SCC)

the patient will benefit from organ-sparing surgery (OSS)

signed broad consent for cancer research

Disqualifiers

N/A

Trial population

Patients with newly diagnosed penile squamous cell carcinoma (SCC), referred to surgical treatment.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Multi-parametric, functional magnetic resonance imaging (MRI)

    Diagnostic test

    Multi-parametric, functional magnetic resonance imaging (MRI) will be performed in all included patients prior to surgery.

Treatment groups

60 Participants
are divided into 1 treatment group
Group A: Patients with penile squamous cell carcinoma.1 intervention

Trial outcomes

Primary outcomes

1

Functional imaging

Assess tumor extent and infiltration depth on multi-parametric MRI (mrT-stage) with histopathological evaluation as a reference standard. Explore usefulness of multi-parametric MRI in assessing inguinal and pelvic lymph nodes (mrN-stage). 2-fluoro-2-deoxy-D-glucose positron emission tomography/computed tomography (FDG PET-CT), sentinel lymph node evaluation and histopathological examination of the resected specimen will be a gold standard.

Time frame
2022-2024

Secondary outcomes

1

Clinical outcome

Assess the locoregional recurrence rate and 5-year survival rate following OSS. Clinical outcome data will be obtained from 5 years clinical follow-up at the Department of Urology OUH.

Time frame
2022-2030
2

Functional outcome

Evaluation of urinary and sexual function following surgery. Functional outcome data will be assessed by urologists using a scoring system and according to the clinical practice, and from interviews with clinical sexologist.

Time frame
2022-2030

Other outcomes

Sponsors and contacts

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