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Completed

NCT Number: NCT03319641

PSMA-PET Imaging for Advanced ACC/SDC

Diagnostic study which evaluates the level of PSMA expression in patients with locally advanced, recurrent and/or metastatic ACC/SDC of ≥18 years old with 68Ga-PSMA-PET/CT imaging in order to establish whether these patients are eligible for 177Lu-PSMA therapy

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Key information

About this study

Rationale: PSMA is a transmembrane protein, which is expressed on prostate cancers cells, ACC and other malignancies. In prostate cancer, distant metastases can be visualized sensitively and non-invasively with 68Ga-PSMA-PET/CT scans and if the uptake of 68Ga is high enough, patients can be treated with the β-emitting radionuclide 177Lu-PSMA. In the current study, we will evaluate the uptake of 68Ga-PSMA by performing 68Ga-PSMA-PET/CT scans in advanced ACC and SDC patients. If the uptake is high enough, this will form the rationale for a therapeutic study with 177Lu-PSMA in ACC and SDC.

Objective: The primary objective is to evaluate the uptake of 68Ga-PSMA in locally advanced, recurrent and metastatic ACC/SDC by performing 68Ga-PSMA-PET/CT scans. The secondary objectives are to calculate the SUV tumor-to-background ratio and tumor-to-'healthy salivary gland tissue' ratio. To correlate the SUV to the degree of immunohistochemical PSMA expression of the primary tumor on archival tissue, and to establish whether new metastatic lesions are found by 68GA-PSMA-PET/CT imaging.

Study design: Diagnostic study which evaluates the level of PSMA expression in ACC/SDC patients with 68Ga-PSMA-PET/CT imaging in order to establish whether these patients are eligible for 177Lu-PSMA therapy.

Study population: Patients with locally advanced, recurrent or metastatic ACC/SDC of ≥18 years old.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • locally advanced, recurrent or metastatic ACC/SDC
  • Age ≥ 18 years old
  • Ability to provide written informed consent

Exclusion criteria

  • Contra-indication for PET imaging
  • Pregnancy
  • Breast feeding
  • Severe claustrophobia
  • Impaired renal function: MDRD <30 ml/min/1,73 m2
  • Impaired liver function: AST and ALT ≥ 2.5 x ULN (≥5 x ULN for patients with liver metastases)

Treatment and study plan

PSMA-PET/CT scan

Diagnostic Test

perform a PSMA-PET/CT scan in patients with locally advanced, recurrent and/or metastastic ACC or SDC

Primary outcomes

  1. uptake of 68Ga-PSMA in ACC and SDC

    Time frame: 0 days

    To evaluate the uptake of 68Ga-PSMA in locally advanced, recurrent and metastatic ACC/SDC by performing 68Ga-PSMA-PET/CT scans

Secondary outcomes

  1. SUV of 68Ga-PSMA in ACC/SDC tumors

    Time frame: 0 days

    SUV of 68Ga-PSMA in ACC/SDC tumors

  2. SUV of 68Ga-PSMA in the background

    Time frame: 0 days

    in order to calculate the SUV tumor to background ratio

  3. correlation of SUV and IHC PSMA-staining

    Time frame: 0 days

    Correlate the tumor uptake (SUV) to the degree of immunohistochemical PSMA expression of the primary tumor on archival tissue

  4. new metastases

    Time frame: 0 days

    To establish whether new metastatic lesions are found by 68GA-PSMA-PET/CT imaging

Sponsors and collaborators

Lead sponsor

Radboud University Medical Center

Other

Collaborators

  • Adenoid Cystic Carcinoma Research Foundation

Registry information

Official study title

68Ga-PSMA-PET/CT Imaging for Locally Advanced, Recurrent and Metastatic Adenoid Cystic Carcinoma or Salivary Duct Carcinoma

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Oct 24, 2017
Registry last updated
May 30, 2018

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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