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Clinical Trials/NCT05667636
NCT05667636
Recruiting
Phase 2

Early Salvage Stereotactic Radiotherapy (esSBRT) for Biochemical Failure After Radical Prostatectomy :a Phase II Study

Regina Elena Cancer Institute1 site in 1 country103 target enrollmentSeptember 27, 2022

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Prostatic Neoplasm
Sponsor
Regina Elena Cancer Institute
Enrollment
103
Locations
1
Primary Endpoint
3-yr BFFS
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

After radical prostatectomy, 30-60% of patients will develop recurrent disease. Salvage radiotherapy, usually at 2 Gy per fraction, is the main treatment option for these patients.

The aim of the present study is to determine the 3-yr biochemical failure free survival of the stereotactic approach in 5 fractions in the context of salvage radiotherapy for biochemical failure after radical prostatectomy.

Detailed Description

The present study aims at delivering 30 Gy to the prostatic bed in 5 fractions. At the same time, the pelvic nodes will be covered to 25 Gy, but in those patients considered at low risk of nodal involvement. In patients with evidence of macroscopic disease at the tumor bed through DCE-MRI, 40 Gy will be delivered in 5 fractions. Selected patients will receive 6-month LHRH analogue preceded by Bicalutamide tablet 50 mg, daily, for 2 weeks to control for possible tumor flare.

Registry
clinicaltrials.gov
Start Date
September 27, 2022
End Date
September 27, 2024
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Giuseppe Sanguineti

Professor

Regina Elena Cancer Institute

Eligibility Criteria

Inclusion Criteria

  • - Able and willing to provide informed consent;
  • Pathologically proven diagnosis of prostatic adenocarcinoma;
  • Biochemical failure (2 consecutive PSA rises above 0.2 ng/ml) after radical prostatectomy;
  • No regional or distant metastases;
  • Eastern Cooperative Oncology Group performance status 0-1

Exclusion Criteria

  • - Previous local treatment of the prostate with radiotherapy, brachytherapy, cryosurgery, high-intensity focused ultrasound or cryotherapy;
  • Previous radiotherapy to the pelvis;
  • Previous or current symptomatic vesicourethral anastomotic stenosis post-RP (weak stream, straining to void, hesitancy and incomplete bladder emptying);
  • PSA level at sRT\> 2 ng/ml;
  • (Each single) Lesion volume within the prostatic fossa at mpMR \>5 cc;
  • Previous chemotherapy for malignancy in past 5 years;
  • Previous androgen deprivation for biochemical failure after RP;
  • Contraindication to short term AD (in case of Px)
  • Presence of nodal or distant metastasis, as confirmed by magnetic resonance (MR) or PET/CT
  • Pathologically positive lymph nodes (pN+) at RP;

Outcomes

Primary Outcomes

3-yr BFFS

Time Frame: 3-years

The primary objective of the study is 3-yr biochemical failure free survival of the stereotactic approach in 5 fractions in the context of salvage radiotherapy for biochemical failure after RP

Secondary Outcomes

  • 3-y OS(3-years)
  • 3-y LC(3-years)
  • 3-y GU GI tox(3-years)
  • 3-y - Patient satisfaction with treatment(3-years)
  • 3-y QoL(3-years)
  • 3-y MFS(3-years)

Study Sites (1)

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