- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07810660
RE-irradiation for Isolated FOCal Recurrence of Prostate Cancer With Ultrahypofracted SBRT (RE-FOCUS)
RE-irradiation for Isolated FOCal Recurrence of Prostate Cancer With Ultrahypofracted SBRT: The RE-FOCUS Study - Pushing the Boundaries of Precision and Efficacy
Panoramica dello studio
Stato
Condizioni
Descrizione dettagliata
One of the most common sites of recurrence is locally in the prostate gland in case of radiotherapy (RT) as primary treatment, and in the prostate bed in case of surgery as primary treatment. In case of PSA persistence or recurrence after surgery as primary treatment, international guidelines recommend salvage RT as the treatment of choice[7]. But what does international guidelines suggest in case of a clinically confirmed local recurrence after an RT course (either curative or salvage)? This presents a significant clinical challenge, as locally radiorecurrent prostate cancer has emerged as the fourth most common genitourinary malignancy in men, following primary prostate cancer, bladder cancer, and kidney cancer[8]. International guidelines recommend various approaches-from monitoring to local therapy (e.g., surgery, high-intensity focused ultrasound, cryotherapy, re-irradiation) or lifelong castration with androgen deprivation therapy (ADT), with a negative impact on patients' quality of life (QoL) due to the wide range of associated side effects. While salvage prostatectomy has been the traditional curative approach, its high morbidity has driven exploration of alternatives like re-irradiation (re-RT) to improve control and reduce adverse events.
Stereotactic body RT (SBRT) has emerged as a promising, curative, non-invasive salvage option, offering precise re-RT with minimal adverse events, as international guidelines suggest. Valle et al.[9] meta-analysis reported no significant differences in 5-year recurrence-free survival among RP, high-intensity focused ultrasound, cryotherapy, and re-RT techniques via brachytherapy (BT) and SBRT. However, re-RT with SBRT was associated with significantly lower genitourinary (GU) adverse events compared to RP, suggesting equivalent efficacy but potentially lower adverse events with re-RT. Similarly, a systematic review on re-RT for local failure after a prior RT showed a safe toxicity profile and promising overall mortality and biochemical control rates[10].
Furthermore, emerging data suggest that partial-prostate re-RT, targeting only the visible recurrent lesion rather than the entire prostate gland or prostate bed, may further reduce severe adverse events without compromising oncological efficacy.
Despite these promising developments, re-RT remains a complex therapeutic challenge requiring careful patient selection, meticulous dosimetric planning, and multidisciplinary clinical management. The cumulative radiation dose to organs at risk (OARs) from both the first radiotherapy course and the second must be carefully evaluated to minimize the risk of severe late adverse events, while delivering sufficient dose to achieve tumor control. Several SBRT techniques for ultrahypofractionated RT (UHRT, defined as >6 Gy per fraction) have been explored. From the early acute adverse events findings of the PACE-B trial, significantly lower RTOG grade 2 or worse GU adverse events were reported in the treatment arm with CyberKnife. This favorable adverse events likely reflects CyberKnife's capability for intrafraction motion management with digitally reconstructed radiographs (DRRs) throughout delivery and real-time beam corrections when deviations exceed tolerance thresholds, which enhance dose conformality to the target volume while improving dose falloff to adjacent OARs. These technical advantages, combined with demonstrated tumor control rates, should position CyberKnife as the preferred SBRT therapy for locally recurrent PCa following a prior RT course.
Tipo di studio
Iscrizione (Stimato)
Contatti e Sedi
Contatto studio
- Nome: BARBARA A JERECZEK-FOSSA, MD, PhD
- Numero di telefono: +39 0257489037
- Email: barbara.jereczek@ieo.it
Backup dei contatti dello studio
- Nome: GIULIA MARVASO, MD
- Numero di telefono: +39 0257489037
- Email: giulia.marvaso@ieo.it
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
Metodo di campionamento
Popolazione di studio
Descrizione
Inclusion Criteria:
- Age > 18 and < 80 years
- Histologically confirmed adenocarcinoma of the prostate initial diagnosis
- History of a previous adjuvant/salvage RT following prostatectomy or curative RT
- Diagnosis of local recurrence at the restaging imaging in hormone sensitive patients (maximum 1 prostate bed recurrence and 3 intraprostatic recurrences)
- DICOM plan of the previous RT course
- No evidence of greater than grade 2 according to Common Terminology Criteria for Adverse Events (CTCAE) genitourinary (GU) or gastrointestinal (GI) late adverse events from the previous RT course
- Eastern Cooperative Oncology Group (ECOG) Performance Status <2
- Good urinary flow (peak flow >10 mL/s) or IPSS < 15
- Written informed consent for treatment and research purpose
Exclusion Criteria:
- Evidence of distant metastasis at the restaging imaging
- Patients with current concomitant anticoagulant therapy (antiplatelet therapy is allowed even if it will be temporary suspended before fiducials implant)
- Platelets count < 75'000/uL
- Urethral stricture
- Having received previous different salvage treatments for PCa local relapse
- Development of BCR while on ADT
- Concomitant inflammatory bowel disease or other serious systemic comorbidities
- Presence of hip prosthesis
- Impossibility of performing an MRI
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Acute GU adverse events
Lasso di tempo: at the end of treatment and 3 months after the end of treatment
|
Acute GU adverse events will be reported as clinician-reported outcomes (according to CTCAE scoring criteria)
|
at the end of treatment and 3 months after the end of treatment
|
|
Acute GI adverse events
Lasso di tempo: at the end of treatment and 3 months after the end of treatment
|
Acute GI adverse events will be reported as clinician-reported outcomes (according to CTCAE scoring criteria)
|
at the end of treatment and 3 months after the end of treatment
|
|
questionnaire IIEF-5
Lasso di tempo: At the baseline and from the end of radiotherapy through study completion, every three months.
|
The patient fills out the questionnaire IIEF-5
|
At the baseline and from the end of radiotherapy through study completion, every three months.
|
|
questionnaire IPSS
Lasso di tempo: At the baseline and from the end of radiotherapy through study completion, every three months.
|
The patient fills out the questionnaire IPSS
|
At the baseline and from the end of radiotherapy through study completion, every three months.
|
|
questionnaire QLQ-C30
Lasso di tempo: At the baseline and from the end of radiotherapy through study completion, every three months.
|
The patient fills out the questionnaire QLQ-C30
|
At the baseline and from the end of radiotherapy through study completion, every three months.
|
|
Late GU adverse events (CTCAE)
Lasso di tempo: From 6 months after the end of radiotherapy until the end of the study, every six months.
|
Late GU adverse events will be reported as clinician-reported outcomes (according to CTCAE scoring criteria)
|
From 6 months after the end of radiotherapy until the end of the study, every six months.
|
|
Late GI adverse events (CTCAE)
Lasso di tempo: From 6 months after the end of radiotherapy until the end of the study, every six months.
|
Late GI adverse events will be reported as clinician-reported outcomes (according to CTCAE scoring criteria)
|
From 6 months after the end of radiotherapy until the end of the study, every six months.
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Biochemical progression-free survival (bPFS)
Lasso di tempo: through study completion, an average of 1 year
|
Defined as the time from the end of re-RT to either biochemical recurrence (BCR) or last follow-up.
bPFS will be assessed through trimestral PSA evaluation from the end of treatment.
|
through study completion, an average of 1 year
|
Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: BARBARA A JERECZEK-FOSSA, MD, PhD, European Institute of Oncology, Milano. Mi, Italy 20141
- Investigatore principale: BARBARA JERECZEK-FOSSA, MD, PhD, European Institute of Oncology, Milano. Mi, Italy 20141
Studiare le date dei record
Studia le date principali
Inizio studio (Stimato)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- UID 5402
- L2-653 (Altro identificatore: Comitato Etico Lombardia 2)
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .