NCT05019846RecruitingPhase 3
SRT Versus SRT+ADT in Prostate Cancer
Stereotactic Prostate Radiotherapy With or Without Androgen Deprivation Therapy, a Phase III, Multi-institutional Randomized-controlled Trial. The SPA Trial.
Source: ClinicalTrials.gov · Last updated 18 Apr 2023 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
To clarify the role of short-term Androgen deprivation therapy (ADT) in the context of intermediate unfavorable and a subclass of high-risk patients treated with prostate Stereotactic radiotherapy (SRT). In intermediate unfavorable risk group, when choosing standard external beam radiotherapy, short term ADT is superior in terms of biochemical disease free survival (bDFS) to EBRT alone. In high risk disease, results of the combination therapy are even more clear. Prostate SRT has been endorsed as option for primary radical treatment for prostate cancer. In such patients, the benefit of ADT is still unknown and the decision is left to clinical judgement. For these reasons, it seems to be relevant to propose a randomized, open label, phase III clinical trial of prostate SBRT + 6 months ADT versus prostate SBRT alone in intermediate unfavorable and a subgroup of high risk prostate cancer patients.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 3
- Study type
- Interventional
- Enrollment
- 310 (estimated)
- First submitted
- 2 Aug 2021
- Start date
- Sept 2021
- Primary completion date
- Dec 2025
- Lead sponsor
- Marco Lorenzo Bonu
- Diseases
- Prostate cancer
- NCT number
- NCT05019846
- EudraCT number
- 2020-005754-23
What you commit to
- Study type: Interventional · Phase 3
- Planned participants: 310
- From Sept 2021 to the primary completion date, Dec 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Previous prostate surgery other than TURP (at least 6 weeks prior to start of SBRT).
- Previous pelvic RT
- Prior androgen deprivation therapy (excluding 5alpha reductase inhibitors)
- Any prior active treatment for prostate cancer; patients on previous active surveillance are eligible if inclusion criteria are met
- Bilateral hip prothesis or any implant that could seriously interfere with dosimetric calculations
- 5alpha reductase inhibitors not discontinued 4 weeks prior to randomization
Other illness
- History of Malignant tumors in the previous 2 years excluding non melanoma cancers of the skin. If a patient presents an anamnesis of malignancy (excluding non melanoma skin cancers) it must be free from disease since 24 months at the time of enrollement.
- Active severe inflammatory bowel disease
- Controindication or hypersensitivity to the use of Triptoreline
- History of bone fractures and fall
Lab values
- Risk factors for abnormal heart rhythms or QT prolongation.
- Use of concomitant medications that prolong the QT/QTc interval
Age
- Age \>80 years.
Other
- cT4a, cT3b or pelvic lymph node involvement
Who the study is looking for
- Histological confirmation of prostate acinar adenocarcinoma with a minimum of 10 biopsy cores taken
- Prostate protocol MRI for local staging
- Patients belonging to intermediate unfavorable group according to the D'Amico/NCCN risk group classification:
- -Grade group 3 or/and
- -2-3 risk factors for intermediate category (PSA 10-20 ng/ml/ Grade group 2-3/ cT2b cT2c) or/and
- -biopsy cores positive ≥50%
- Patients belonging to a subclass of high risk group according to the D'Amico/NCCN risk group classification:
- -ISUP group 4 (GS 4+4, 3+5, 5+3) or
- -cT3a stage or
- PSA\>20
- Eastern Coooperative Oncology Group (ECOG) PS 0-2
- Ability of the patient to understand and sign a written informed consent document
- Ability and willingness to comply with patients reported outcome questionnaires schedule during the study time
- IPSS 0-15
- Prostate Volume less than 100cc
- PSA must be dosed maximum 60 days before randomization
- No pathologic lymph nodes and distant metastasis on PET (fluorocholine) scan or CT scan+bone scan.
- Contraceptive measures for patients with partners with reproductive potential must be explained
Age in the registry: 18 years to 80 years · Sex: Male · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| ASST Spedali Civili of Brescia Coordinator of this site? Confirm its status | Brescia | Italy | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.