Expanded Access Ga68 PSMA PET Imaging

Overview

Información sobre este estudio

The primary objective of this study is to provide access to [Ga-68] PSMA-11 imaging (PET/CT or PET/MR) for patients diagnosed with untreated high-risk prostate cancer or biochemically recurrent prostate cancer.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria -
Patients with Untreated High Risk Prostate Cancer:

Patients with prostate cancer, who have not received anticancer therapy and who meet at least one of the following criteria for high-risk prostate cancer are eligible for inclusion in this expanded access IND study:

  • Serum prostate-specific antigen (PSA) concentration of 20 ng/mL or more.
  • Pathologic criteria of International Society of Uropathology (ISUP) grade group 3–5: ISUP grades 3-5 are equivalent to pathologic Gleason scores of 4+3, 8, 9 or 10.
  • Local staging of T3 or worse, indicating that cancer has invaded into tissues outside of the prostate gland, as seen at either CT or MRI.

Inclusion Criteria - 
Patients with Biochemically Recurrent Prostate Cancer:

Patients with prostate cancer, who have undergone initial anticancer therapy in the form of surgery or radiation and who meet at least one of the following criteria are eligible for inclusion in this expanded access IND study:

  • In patients who are post prostatectomy, a PSA > 0.2ng/mL on 2 consecutive tests;
  • In patients who have undergone definitive prostate radiation, a PSA rise ≥ 2.0 ng/mL above nadir PSA.

Exclusion Criteria:

  • Patients unable to provide informed consent.
  • Patients with a life expectancy less than 6 months.
  • Additional exclusion criteria may be added based on demand.

 

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Rochester, Minn.

Investigador principal de Mayo Clinic

Geoffrey Johnson, M.D., Ph.D.

Cerrado para la inscripción

Contact information:

Casey Burns

Burns.Casey@mayo.edu

More information

Publicaciones

Publications are currently not available
.
CLS-20509688

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