About this trial

This phase III trial tests two questions by two separate comparisons of therapies. The first question is whether enhanced therapy (apalutamide in combination with abiraterone + prednisone) added to standard of care (prostate radiation therapy and short term androgen deprivation) is more effective compared to standard of care alone in patients with prostate cancer who experience biochemical recurrence (a rise in the blood level of prostate specific antigen \[PSA\] after surgical removal of the prostate cancer).

A second question tests treatment in patients with biochemical recurrence who show prostate cancer spreading outside the pelvis (metastasis) by positron emission tomography (PET) imaging. In these patients, the benefit of adding metastasis-directed radiation to enhanced therapy (apalutamide in combination with abiraterone + prednisone) is tested.

Diagnostic procedures, such as PET, may help doctors look for cancer that has spread to the pelvis. Androgens are hormones that may cause the growth of prostate cancer cells. Apalutamide may help fight prostate cancer by blocking the use of androgens by the tumor cells. Metastasis-directed targeted radiation therapy uses high energy rays to kill tumor cells and shrink tumors that have spread. This trial may help doctors determine if using PET results to deliver more tailored treatment (i.e., adding apalutamide, with or without targeted radiation therapy, to standard of care treatment) works better than standard of care treatment alone in patients with biochemical recurrence of prostate cancer.

Eligibility criteria

Qualifiers

STEP 0: REGISTRATION ELIGIBILITY CRITERIA

Patient must be male and >= 18 years of age.

Patient must have had a radical prostatectomy (RP) as definitive therapy for histopathologically-proven prostatic adenocarcinoma

If time to BCR, defined as time to first detectable PSA ( > lower limit of normal for assay used) after RP, is < 12 months, a minimum PSA level of >= 0.2 ng/mL and a confirmatory reading of >= 0.2 ng/mL is required, per the American Urological Association (AUA) definition (Note: patients with a persistent PSA reading of at least 0.2 ng/mL are eligible)

Disqualifiers

None

Trial design

Treatments tested in this trial

  • 3-Dimensional Conformal Radiation Therapy
  • Apalutamide
  • Computed Tomography
  • Degarelix
  • External Beam Radiation Therapy
  • Fluciclovine F18
  • Goserelin Acetate
  • Intensity-Modulated Proton Therapy
  • Intensity-Modulated Radiation Therapy
  • Leuprolide Acetate
  • Magnetic Resonance Imaging
  • Positron Emission Tomography
  • Quality-of-Life Assessment
  • Questionnaire Administration
  • Relugolix
  • Stereotactic Body Radiation Therapy
  • Triptorelin
  • Volume Modulated Arc Therapy

Treatment groups

804 Participants
are divided into 4 treatment groups

Locations

342
Alaska
Alaska Breast Care and Surgery LLC99508, Anchorage United States
Alaska Oncology and Hematology LLC99508, Anchorage United States
Alaska Women's Cancer Care99508, Anchorage United States
Anchorage Associates in Radiation Medicine98508, Anchorage United States

Sponsors and collaborators

ECOG-ACRIN Cancer Research Group

Lead sponsor

National Cancer Institute (NCI)

Collaborator