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RE-irradiation for Isolated FOCal Recurrence of Prostate Cancer With Ultrahypofracted SBRT (RE-FOCUS)

4 września 2026 zaktualizowane przez: European Institute of Oncology

RE-irradiation for Isolated FOCal Recurrence of Prostate Cancer With Ultrahypofracted SBRT: The RE-FOCUS Study - Pushing the Boundaries of Precision and Efficacy

Prostate cancer (PCa) is one of the most frequently diagnosed malignancies in men worldwide, with the highest prevalence observed in developed countries. Patients affected by localized disease can be treated with several local modalities, including radical prostatectomy (RP), external beam radiotherapy (EBRT) and brachytherapy (BT). Although the advances in treatment strategies, after primary treatment 5 to 60% of men experience biochemical recurrence (BCR).

Przegląd badań

Status

Jeszcze nie rekrutacja

Warunki

Szczegółowy opis

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.

Typ studiów

Obserwacyjny

Zapisy (Szacowany)

60

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

Kopia zapasowa kontaktu do badania

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie

Metoda próbkowania

Próbka bez prawdopodobieństwa

Badana populacja

All enrolled patients will receive standard-of-care CyberKnife-based SBRT to the pelvic target. Androgen deprivation therapy (ADT), including its indication, timing, and duration, will be prescribed at the discretion of the treating radiation oncologist based on clinical judgment and individual patient characteristics.

Opis

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

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Acute GU adverse events
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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.

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Biochemical progression-free survival (bPFS)
Ramy czasowe: 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

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Śledczy

  • Główny śledczy: BARBARA A JERECZEK-FOSSA, MD, PhD, European Institute of Oncology, Milano. Mi, Italy 20141
  • Główny śledczy: BARBARA JERECZEK-FOSSA, MD, PhD, European Institute of Oncology, Milano. Mi, Italy 20141

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Szacowany)

1 września 2026

Zakończenie podstawowe (Szacowany)

1 maja 2030

Ukończenie studiów (Szacowany)

1 maja 2030

Daty rejestracji na studia

Pierwszy przesłany

31 sierpnia 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

4 września 2026

Pierwszy wysłany (Rzeczywisty)

9 września 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

9 września 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

4 września 2026

Ostatnia weryfikacja

1 lipca 2026

Więcej informacji

Terminy związane z tym badaniem

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

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