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NCT Number: NCT06867588

The Added-value of PSMA PET in Detecting Clinically Significant Prostate Cancer Lesions in Patients Undergoing MRI-targeted Biopsy. (PANDORA)

Prostate Specific Membrane Antigen (PSMA) positron emission tomography/computed tomography (PET/CT), an imaging modality focusing on a protein overexpressed by prostate cancer cells, has revolutionised the staging of both newly diagnosed and biochemically recurrent prostate cancer with better performance when compared to conventional imaging. Indeed, several studies have shown that PSMA PET/CT outperformed choline PET/CT with better detection rate of metastatic disease, particularly in the setting of disease recurrence after therapy even at (very) low PSA level. Moreover, the proPSMA trial reported that PSMA PET/CT had 27% greater accuracy than that of CT and bone scanning when staging patients with high-risk localised prostate cancer. More recently, availability of integrated PET/MRI scanners offers the opportunity for higher accuracy imaging and promising diagnostic studies. It also offers enhanced spatial integration that resulting in better contouring and targeting of prostate lesions.

In the light of current issues, the next question is whether PSMA PET imaging could add to the detection of prostate cancer. Several retrospective case-report studies reported promising results regarding the improved diagnostic accuracy of prostatic PSMA PET/CT . Recently, in the PRIMARY trial, 291 men received successively MRI, PSMA PET/CT and systematic ± MRI-targeted biopsies. Despite similar PPV between imaging methods, the main advantage of PSMA was in men with equivocal MRI. Indeed, they found that 90% of csPCa was identified by PSMA PET/CT in this subgroup and paved the way for further investigation. This finding was confirmed in the most recent systematic review and meta-analysis.

The aim of this prospective study is to evaluate the added-value of PSMA PET in detecting prostate cancer in patients who are candidates for biopsy with equivocal MRI.

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Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Institut Jules Bordet

Brussels, 1070, Belgium

Location status: Recruiting

Location contact

Loubna TARAJI

CONTACT

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Subjects must meet the following criteria for inclusion in the study:

  • Men ≥ 18 years of age
  • Multiparametric MRI within the previous 6 months
  • At least one lesion PI-RADS 3
  • Able to provide written informed consent

Exclusion criteria

Eligible subjects must not meet any of the exclusion criteria listed below:

  • Previous prostate cancer diagnostic on MRI-targeted biopsy
  • At least one lesion PI-RADS 4-5
  • Negative MRI (PI-RADS 1-2)
  • Previous treatment for prostate cancer 11
  • Contraindication to PSMA PET and/or MRI and/or prostate biopsy
  • Low quality of MRI defined by a PI-QUAL score of 1 or 2
  • Any medical condition that may interfere with the study procedures.

Treatment and study plan

PSMA PET

Diagnostic Test

patients included in the study will perfom a PSMA PET

Primary outcomes

  1. Percentage of patients with clinically significant prostate cancer detected by PSMA PET-targeted biopsy

    Time frame: Baseline

Study contacts

Contact information is provided by the study sponsor or research team.

Loubna Taraji

CONTACT

[email protected]

003225413781

Romain Diamand

CONTACT

[email protected]

003225413781

Sponsors and collaborators

Lead sponsor

Jules Bordet Institute

Other

Registry information

Official study title

The Added-value of PSMA PET in Detecting Clinically Significant Prostate Cancer Lesions in Patients Undergoing MRI-targeted Biopsy. (PANDORA): a Prospective, Paired Diagnostic Study

Acronym: PANDORA

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Mar 10, 2025
Registry last updated
Mar 31, 2025

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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