About this trial

This phase II trial tests how well carboplatin before surgery works in treating patients with high-risk prostate cancer and an inherited BRCA1 or BRCA2 gene mutation. Carboplatin is in a class of medications known as platinum-containing compounds. It works in a way similar to the anticancer drug cisplatin, but may be better tolerated than cisplatin. Carboplatin works by killing, stopping, or slowing the growth of tumor cells. Giving carboplatin before surgery may shrink tumors in patients with high-risk prostate cancer with BRCA1 and BRCA2 gene mutations.

Eligibility criteria

Qualifiers

Participant must have histologic diagnosis of prostate adenocarcinoma

cT3a - cT4x

Grade group 4 or 5 (Gleason sum 8-10)

PSA > 20 ng/mL prior to registration

Disqualifiers

Participant must not have evidence of distant metastatic disease by conventional imaging within 90 days prior to registration

NOTE: cN1 detected only by PSMA-PET is permitted if urologist deems sites of disease to be potentially completely resectable

Participant must not have received prior radiation therapy (RT) to the pelvic region

Participant must not have a prior or concurrent malignancy whose natural history or treatment (in the opinion of the treating physician) has the potential to interfere with the safety or efficacy assessment of protocol treatment

Trial design

Treatments tested in this trial

  • Biospecimen Collection
  • Carboplatin
  • Chest Radiography
  • Computed Tomography
  • Magnetic Resonance Imaging
  • PSMA PET Scan
  • Surgical Procedure

Treatment groups

44 Participants
are divided into 1 treatment group

Locations

133
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

SWOG Cancer Research Network

Lead sponsor

National Cancer Institute (NCI)

Collaborator