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

2026년 9월 4일 업데이트: 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).

연구 개요

상태

아직 모집하지 않음

정황

상세 설명

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.

연구 유형

관찰

등록 (추정된)

60

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 연락처 백업

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

샘플링 방법

비확률 샘플

연구 인구

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.

설명

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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Acute GU adverse events
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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)
기간: 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)
기간: 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.

2차 결과 측정

결과 측정
측정값 설명
기간
Biochemical progression-free survival (bPFS)
기간: 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

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

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

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 9월 1일

기본 완료 (추정된)

2030년 5월 1일

연구 완료 (추정된)

2030년 5월 1일

연구 등록 날짜

최초 제출

2026년 8월 31일

QC 기준을 충족하는 최초 제출

2026년 9월 4일

처음 게시됨 (실제)

2026년 9월 9일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 9월 9일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 9월 4일

마지막으로 확인됨

2026년 7월 1일

추가 정보

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미국 FDA 규제 의약품 연구

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아니

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