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Идёт набор NCT06867588

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

Без фазы С лечением Multiparametric MRI Lesion PI-RADS 3

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: PSMA PET.
Кому может быть актуально
Состояния в реестре: Multiparametric MRI, Lesion PI-RADS 3. Базовые параметры: от 18 лет · Мужчины.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Бельгия
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

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

Обзор

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.

Вмешательства

  • Диагностический тест PSMA PET
    patients included in the study will perfom a PSMA PET

Первичные конечные точки

  • Percentage of patients with clinically significant prostate cancer detected by PSMA PET-targeted biopsy [Срок оценки: Baseline]

Критерии участия

Критерии включения

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

Критерии исключения

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.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Не применимо
Модель
Одна группа
Маскирование
Открытое
Основная цель
Диагностика

Центры проведения

Бельгия · 1 центр
  • Institut Jules Bordet — Brussels

Идентификаторы

NCT: NCT06867588 · IJBPANDORA

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗