Denne side blev automatisk oversat, og nøjagtigheden af ​​oversættelsen er ikke garanteret. Der henvises til engelsk version for en kildetekst.

Relugolix in Patients With High-risk, Localized or Locally Advanced Prostate Cancer Who Are Candidates for Radical Prostatectomy. (HEROIC)

3. november 2026 opdateret af: Istituto Oncologico Veneto IRCCS

A Randomized, Controlled, Phase 3 Study of Relugolix in Patients With High-risk, Localized or Locally Advanced Prostate Cancer Who Are Candidates for Radical Prostatectomy.

This study is designed to evaluate the efficacy of Relugolix for 3 months before radical prostatectomy + lymph node dissection followed by 6 months Relugolix versus radical prostatectomy + lymphnode dissection followed by 6 months Relugolix. Relugolix is an oral highly selective LHRH antagonist given daily that has been shown to achieve androgen deprivation in both phase I and phase II trials and was finally approved in the phase III HERO trial.

Relugolix is approved in the United States (US) and Europe for the treatment of advanced prostate cancer.

The HERO trial enrolled patients with castration sensitive prostate cancer and compared their sustained castration rate at 48weeks to leuprolide. While the safety profile of the 2 agents was similar, relugolix achieved castrate levels of testosterone faster and provided a higher overall rate of castration. In the phase III HERO trial, relugolix demonstrated suppression of testosterone concentrations to castration levels in 96.7% of patients from Day 29 through 48 weeks, which was superior to leuprolide and resulted in a 54% lower risk of major adverse cardiovascular events. Relugolix also demonstrated superior efficacy to leuprolide for key secondary endpoints, including the cumulative probability of testosterone suppression to castrate levels (< 50 ng/dL) on day 4 and on day 15, PSA response (> 50% decrease) at day 15 with confirmation at day 29, the cumulative probability of testosterone suppression to profound castrate levels (< 20 ng/dL) on day 15, and mean FSH level at the end of week 24. Testosterone recovery was investigated in a subgroup of patients (n = 184): 54% of relugolix recipients versus 3% of leuprolide recipients had testosterone recovery to ≥ 280 ng/dL 90 days after completing 48 weeks of treatment.Relugolix was generally well tolerated in men with prostate cancer, with most adverse events being consistent with physiologic effects of testosterone suppression. Most adverse events were of grade 1 or 2 severity. In a phase II study comparing relugolix to degarelix the global health status, as assessed by EORTC-QLQ-C30, and sexual activity and hormonal treatment-related symptoms, as assessed by the EORTC-QLQ-PR25, were negatively affected during treatment in both groups. Within 12 wk after treatment discontinuation, sexual activity scores improved by a mean of 12.1 for relugolix and 6.6 for degarelix and hormonal treatment-related symptoms changed by a mean of -5.0 and -1, respectively. Similarly, AMS total and subscale scores (sexual, psychological, and somatic) worsened during treatment in both groups but after treatment discontinuation, the mean percentage change in AMS total scores was -15% in the relugolix group and -2.9% in the degarelix group.

The fast testosterone recovery with relugolix was associated with a rapid improvement in a range of castration-related symptoms on QoL measures.

Building upon the practice-changing evidence established by the PROTEUS trial, evaluating oral Relugolix as a perioperative backbone in high-risk patients candidate for radical prostatectomy offers distinct pharmacological, safety, and patient-centered advantages. While PROTEUS validated the clinical benefit of perioperative androgen receptor pathway modulation, Relugolix provides rapid and profound testosterone suppression without an initial surge, paired with a significantly lower cardiovascular risk profile and markedly accelerated post-treatment testosterone and Quality of Life (QoL) recovery compared to standard LHRH agonists. In the HEROIC trial, testing a 3-month neoadjuvant Relugolix induction phase prior to surgery followed by 6 months of adjuvant Relugolix (Arm A) versus immediate surgery followed by 6 months of adjuvant Relugolix (Arm B) addresses whether an all-oral GnRH antagonist strategy can reproduce perioperative oncological downstaging and improve Biochemical Recurrence-Free Survival (bRFS) while optimizing cardiovascular safety and patient recovery.

Studieoversigt

Status

Ikke rekrutterer endnu

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

268

Fase

  • Fase 3

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Undersøgelse Kontakt Backup

Studiesteder

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 99 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Han

Beskrivelse

Inclusion Criteria:

  • Male who are at least 18 Years on the day of signing informed consent;
  • Candidate for radical prostatectomy (RP);
  • Adequate organ function (hepatic, renal, hematologic and cerebral) determined at the discretion of the treating physician;
  • Eastern Cooperative oncology Group (ECOG) Performance Status Score of 0 or 1
  • High risk PCa [biopsy Gleason score 8-10 {ISUP GG 4-5}, PSA >20 ng/ml, cT2c [MRI based], and/or cN1 disease) or non onrgan confined disease defined as cT3-4 and/or cN + [MRI based] any ISUP grade any PSA and were amenable to RP + extended pelvic lymph node dissection (ePLND). A minimun score of Gleason 7(4+3) will be allowed.
  • Staging with PSMA PET/CT (systemic and local) and mpMRI of the prostate and pelvis (as mandatory prebiopsy staging procedure).

Exclusion Criteria:

  • History or presence of soft tissue/bone metastasis or metastasis in distant lymph nodes (pelvic lymph nodes below the iliac bifurcation that are less than (<) 2 centimetres (cm) in diameter [short axis] either radiographically or pathologically are allowed.)
  • History of bilateral orchiectomy
  • Prior or current radiation therapy for treatment of prostate cancer
  • Received an investigational intervention ≤ 4 weeks before the planned first dose of study intervention
  • History of seizure or condition that may predispose to seizure (including, but not limited to prior stroke, transient ischemic attack or loss of consciousness ≤1 year prior to randomization; brain arteriovenous malformation; or intracranial masses such as schwannomas and meningiomas that are causing edema or mass effect)
  • Active or symptomatic viral hepatitis or chronic liver disease or HIV
  • History of pituitary or adrenal dysfunction
  • Clinically significant heart disease as evidenced by myocardial infarction, or arterial thrombotic events in the past 6 months, severe or unstable angina, or New York Heart Association (NYHA) Class II-IV heart disease or cardiac ejection fraction measurement of <50% at baseline
  • Other malignancy
  • Any condition, which, in the opinion of the investigator, would preclude participation in this trial
  • Gastrointestinal conditions affecting Absorption
  • Hypersensitivity to the active substance or to any of the excipients of the study medication
  • Any psychological, cognitive, familial, sociological or geographical condition that, in the investigator's opinion, compromises the patient's ability to understand the patient information, to give informed consent or to comply with the study protocol
  • Participation in another interventional clinical trial during this trial or within 4 weeks before entry into this trial. There may be exceptions at the discretion of the (coordinating) investigator
  • Any clinical contraindication to experimental drug adoption as per physician discretion

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Crossover opgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Arm A (Experimental)

Relugolix orally (loading dose of 360 mg on Day 1, followed by 120 mg once daily) as neoadjuvant therapy for 3 months prior to radical prostatectomy (RP) with extended pelvic lymphadenectomy (ePLND). Subsequently, post-operative adjuvant treatment with Relugolix for 6 months (loading dose 360 mg, followed by 120 mg/day).
Medicin: Relugolix-Neoadjuvant treatment

The perioperative treatment will be based on 3 months of Androgen Deprivation Therapy (ADT) with relugolix 120 mg followed by radical prostatectomy (RP) and lymph node dissection.

The Relugolix administration will be based on a loading dose of 360 mg, corresponding on 3 tablets, on the first day followed by a 120 mg (one tablet) dose taken once daily at approximately the same time each day.

Relugolix can be taken with or without food. Tablets should be taken with some liquid as needed and should be swallowed whole.
Aktiv komparator: Arm B (Control)

Immediate undergoing radical prostatectomy (RP) with extended pelvic lymphadenectomy (ePLND), followed by 6 months of post-operative adjuvant treatment with oral Relugolix (loading dose of 360 mg on Day 1, followed by 120 mg once daily).
Medicin: Relugolix-Adjuvant treatment

Patients allocated on control arm will receive only postoperative treatment. Postoperative treatment will be based on 6 months of relugolix 120 mg after RP.

The Relugolix administration will be based on a loading dose of 360 mg, corresponding on 3 tablets, on the first day, followed by a 120 mg (one tablet) dose taken once daily at approximately the same time each day.

Relugolix can be taken with or without food. Tablets should be taken with some liquid as needed and should be swallowed whole.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Biochemical Recurrence-Free Survival (bRFS)
Tidsramme: Through study completion, an average of 3 years

Biochemical Recurrence-Free Survival (bRFS) defined as the time from randomization to the first documented evidence of biochemical recurrence, measured as:

  • A confirmed serum PSA value ≥ 0.2 ng/mL after radical prostatectomy (two consecutive determinations at least 3 weeks apart), or
  • The clinical decision to initiate salvage therapy (radiotherapy or systemic therapy) for a documented biochemical recurrence (any non-protocol defined treatment)
  • Any new evidence of metastatic disease on bone or PSMA PET/mpMRI [imaging modalities as per physician or multidisciplinary team decision's discretion]
  • Any local recurrence in the prostate bed, as determined by PSMA PET/ mpMRI; [imaging modalities as per physician or multidisciplinary team decision's discretion].

Patients without an event will be censored at the date of their last PSA assessment.
Through study completion, an average of 3 years

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Metastasis-Free Survival (MFS)
Tidsramme: Through study completion, an average of 3 years

MFS will be defined as the time from randomization to the first radiological evidence of distant metastasis (confirmed by blinded independent central review, BICR) or death from any cause.
Through study completion, an average of 3 years
Pathological Complete Response (pCR)
Tidsramme: Through study completion, an average of 3 years

pCR will be defined as no residual tumor ypT0 detected in the prostatectomy specimen, as assessed by a pathology BICR);
Through study completion, an average of 3 years
Minimal Residual Disease (MRD)
Tidsramme: Through study completion, an average of 3 years

MRD will be defined as presence of residual tumor ≤ 5 mm in maximal cross-sectional dimension provided it is confined to the prostate, i.e. ypT2 or lower. The primary pathology assessment will be performed by a blinded independent central review (BICR).
Through study completion, an average of 3 years
Overall Survival (OS)
Tidsramme: Through study completion, an average of 3 years

Overall Survival (OS) will be defined as time from randomization to death from any cause
Through study completion, an average of 3 years
Time to Castration-Resistant Prostate Cancer (CRPC)
Tidsramme: Through study completion, an average of 3 years

Time to Castration-Resistant Prostate Cancer (CRPC) will be evaluated as time from randomization to evidence of disease progression at CRPC
Through study completion, an average of 3 years
Time to First Salvage Therapy (Radiotherapy or systemic)
Tidsramme: Through study completion, an average of 3 years

Time to First Salvage Therapy will be evaluated as time from randomization to the start date of the first systemic therapy or radiotherapy (RT)
Through study completion, an average of 3 years
Testosterone suppression and recovery
Tidsramme: Through study completion, an average of 3 years

Testosterone suppression and recovery will be defined as:

o Proportion of patients achieving testosterone ≤ 50 ng/dL and ≤ 20 ng/dL during treatment.
Through study completion, an average of 3 years
Testosterone suppression and recovery
Tidsramme: Through study completion, an average of 3 years

Testosterone suppression and recovery will be defined as:

o Time to testosterone recovery (≥ 280 ng/dL) after treatment discontinuation.
Through study completion, an average of 3 years
PSA kinetics
Tidsramme: Through study completion, an average of 3 years

PSA kinetics will be evaluated as proportion of patients achieving ≥ 90% PSA reduction from baseline, and PSA < 0.2 ng/mL at Week 25.
Through study completion, an average of 3 years
Quality of Life (QoL)
Tidsramme: Through study completion, an average of 3 years

Quality of Life (QoL) will be assessed by EORTC-QLQ-C30 domain scores at ICF signing, at the end of perioperative period (for Arm A), at 15 days from RP; 4 weeks post-RP; 12 weeks post-RP; End Of Treatment; 12 weeks post-EOT; 6 months post-EOT; 12 months post-EOT
Through study completion, an average of 3 years
Quality of Life (QoL)
Tidsramme: Through study completion, an average of 3 years

Quality of Life (QoL) will be assessed by EORTC-QLQ-PR25 domain scores at ICF signing, at the end of perioperative period (for Arm A), at 15 days from RP; 4 weeks post-RP; 12 weeks post-RP; End Of Treatment; 12 weeks post-EOT; 6 months post-EOT; 12 months post-EOT
Through study completion, an average of 3 years
Safety and tolerability of Relugolix
Tidsramme: Through study completion, an average of 3 years

Safety and tolerability during the treatment will be recorded and graded according to the NCI-Common Terminology Criteria for Adverse Events (CTCAE) v.5. Grade refers to the severity of the adverse event. A grading (severity) scale is provided for each adverse event term. The CTCAE displays Grades 1 through 5 with unique clinical descriptions of severity for each AE. Safety and tolerability will be evaluated also as laboratory, ECG abnormalities and cardiovascular events (MACE).
Through study completion, an average of 3 years

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Istituto Oncologico Veneto IRCCS

Samarbejdspartnere

Accord Healthcare Italia S.r.l.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

31. januar 2027

Primær færdiggørelse (Anslået)

31. januar 2030

Studieafslutning (Anslået)

29. december 2031

Datoer for studieregistrering

Først indsendt

27. oktober 2026

Først indsendt, der opfyldte QC-kriterier

3. november 2026

Først opslået (Faktiske)

10. november 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

10. november 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

3. november 2026

Sidst verificeret

1. november 2026

Mere information

Begreber relateret til denne undersøgelse

Nøgleord

Andre undersøgelses-id-numre

  • IOV- PR-01-2024 HEROIC
  • 2025 (U.S. NIH-bevilling/kontrakt)
  • 2025-524702-15-00 (Ctis)

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Abonner