Hypofractionated Radiotherapy with a Focal Microboost for the Treatment of High-Risk and Locally Advanced Prostate Cancer

Inclusion Criteria

• Provision of signed and dated informed consent form
• Stated willingness to comply with all study procedures and availability for the duration of the study
• Biologically male patients aged 18 years and older
• Ability to receive pelvic radiotherapy and be willing to adhere to the protocol regimen
• Previously untreated prostate cancer (with cytotoxic chemotherapy, cryotherapy, ablative treatment, surgical or radiation therapy). Prior transurethral resection of prostate (TURP) is permitted if 90 days or more prior to the start of radiotherapy
• Localized or locally advanced prostate cancer meeting National Comprehensive Cancer Network (NCCN) criteria for high risk, very high risk or non-metastatic, pelvic lymph node positive defined as having at least one or more of the following: * Prostate specific antigen (PSA) >20 ng/mL prior to starting ADT. * cT3a-T4 by digital exam or imaging. * Gleason score of 8-10 (grade group 4 or 5). * Staged as N1M0 by the treating investigator (pelvic lymph node positive, below the aortic bifurcation) based on soft tissue imaging within 120 days prior to registration (may include CT, MRI or PSMA PET/CT, of fluciclovine choline PET/CT)
• History and physical exam within 120 days prior to registration
• Eastern Cooperative Oncology Group (ECOG) performance status 0-2
• Be able to undergo MRI of the prostate and/or pelvis as a component of RT planning
• Have at least one MRI visible target for microboost (Prostate Imaging-Reporting and Data System [PI-RADS] ≥ 4 version 2.0)
• Bone and soft tissue imaging as clinically indicated for staging within 120 days prior to registration
• For males: use of condoms or other methods to ensure effective contraception with partner during radiation and for six months after completion of radiation
• Hemoglobin >= 9.0 g/dL independent of transfusion (within 120 days prior to registration)
• Platelet count >= 100,000 x 10 ^9/microliter independent of transfusion (within 120 days prior to registration)
• Total bilirubin < 2 x institutional upper limits of normal (ULN is 1.2 mg/dL). If labs are done at outside institution, total bilirubin should be < 2.4 (within 120 days prior to registration)
• Agreeable and eligible to receive long term (defined as 12-36 months) ADT as a standard component of prostate cancer therapy

Exclusion Criteria

• Concurrent use of testosterone supplementation unless discontinued by time of registration
• Definitive radiologic evidence of metastatic disease outside of the pelvic nodes on conventional imaging (bone scan, CT scan, MRI)
• Prior pelvic radiotherapy
• Pre-existing conditions or overall health status which disqualifies the patient from curative intent-RT. Patients with life expectancy less than 5 years are not eligible
• Treatment with another investigational prostate cancer therapy within 12 months
• Prior total prostatectomy, cryotherapy, high-intensity focused ultrasound, irreversible electroporation, MRI ablation, laser ablation, transurethral ultrasound ablation, aquablation directed towards the prostate for any prostate disease or condition
• Prior or concurrent invasive pelvic malignancy (except non-melanomatous skin cancer) or lymphomatous or hematogenous malignancy, unless disease free for a minimum of 5 years
• Any condition that, in the opinion of the investigator, would preclude participation in this study
• Prior pharmacologic androgen ablation for prostate cancer is allowed only if the onset of androgen ablation (both luteinizing hormone-releasing hormone [LHRH] agonist and oral anti-androgen) is ≤ 90 days prior to registration
• Inability to undergo implantation of gold fiducial markers or rectal spacer gel
• Patients with a prior or concurrent malignancy whose natural history or treatment has the potential to interfere with the safety or efficacy assessment of the investigational regimen