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PSMA PET/CT-Guided SBRT Plus Darolutamide in mHSPC (PSMA-DaroRT)

6. september 2026 oppdatert av: Hao Zeng, West China Hospital

A Multicenter, Prospective, Randomized Controlled Phase II Trial of PSMA PET/CT-Guided Stereotactic Body Radiotherapy Combined With Darolutamide and Androgen Deprivation Therapy in Patients With Metastatic Hormone-Sensitive Prostate Cancer

This is a multicenter, randomized, open-label phase 2 study for men with metastatic hormone-sensitive prostate cancer. About 254 participants will first receive 6 months of darolutamide plus androgen deprivation therapy. Participants whose cancer has not progressed and who still have active tumor lesions on prostate-specific membrane antigen positron emission tomography/computed tomography (PSMA PET/CT) will then be randomly assigned to one of two groups. One group will continue darolutamide plus androgen deprivation therapy. The other group will receive stereotactic body radiotherapy (SBRT) to all active tumor lesions identified by PSMA PET/CT, while continuing darolutamide plus androgen deprivation therapy. The main purpose of this study is to find out whether adding PSMA PET/CT-guided SBRT can help participants live longer without tumor growth seen on scans or death. The study will also evaluate prostate-specific antigen (PSA) changes, time to castration-resistant prostate cancer, overall survival, side effects, and quality of life.

Studieoversikt

Detaljert beskrivelse

Metastatic hormone-sensitive prostate cancer is usually treated with systemic therapy, including androgen deprivation therapy and androgen receptor pathway inhibitors such as darolutamide. However, some patients still have active tumor lesions after initial systemic treatment, and these residual lesions may contribute to later disease progression.

This study is designed to test whether adding targeted radiotherapy to residual active tumor lesions can improve disease control. All enrolled participants will first receive 6 months of darolutamide plus androgen deprivation therapy. After this initial treatment period, participants will undergo clinical and imaging assessment, including prostate-specific membrane antigen positron emission tomography/computed tomography (PSMA PET/CT), to evaluate whether active tumor lesions remain.

Participants who have no disease progression and still have PSMA PET/CT-positive active tumor lesions will be randomly assigned in a 1:1 ratio to one of two groups. Participants in the control group will continue darolutamide plus androgen deprivation therapy. Participants in the experimental group will continue darolutamide plus androgen deprivation therapy and will also receive stereotactic body radiotherapy (SBRT) to all active tumor lesions identified by PSMA PET/CT, including active lesions in the prostate or prostate bed and metastatic sites when appropriate.

This is a multicenter, prospective, randomized, open-label phase 2 study. The study plans to enroll about 254 men with metastatic hormone-sensitive prostate cancer. The main question is whether PSMA PET/CT-guided SBRT, when added to darolutamide and androgen deprivation therapy after 6 months of initial systemic treatment, can increase the proportion of participants who are alive without radiographic disease progression at 3 years after randomization.

Participants will be followed regularly with physical examinations, blood tests including prostate-specific antigen (PSA), testosterone monitoring when required, imaging examinations, assessment of adverse events, and quality-of-life questionnaires. Imaging-based disease progression will be assessed using standard criteria for soft tissue and bone lesions. Safety will be monitored throughout the study, including side effects related to darolutamide, androgen deprivation therapy, and radiotherapy.

The study will also explore whether PSMA PET/CT imaging features, PSA changes, circulating tumor DNA, and molecular features of tumor or blood samples are associated with treatment response, disease progression, or survival outcomes. These exploratory analyses may help identify future biomarkers for selecting patients who are more likely to benefit from combined systemic therapy and PSMA PET/CT-guided radiotherapy.

Studietype

Intervensjonell

Registrering (Antatt)

254

Fase

  • Fase 2

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

    • Sichuan
      • Chengdu, Sichuan, Kina, 610041
        • West China Hospital, Sichuan University

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

Inclusion Criteria:

  • Male participants aged ≥18 years and <85 years.
  • Histologically confirmed prostate adenocarcinoma.
  • No neuroendocrine carcinoma, ductal adenocarcinoma, small-cell carcinoma, signet-ring cell carcinoma, or sarcomatoid carcinoma component.
  • Metastatic prostate cancer confirmed by imaging and/or pathological evidence.
  • Baseline PSMA PET/CT assessment demonstrates a total of ≤20 metastatic lesions.
  • No prior radical prostatectomy or radiotherapy for prostate cancer.
  • No prior systemic anti-tumor therapy that may affect the efficacy assessment of this study, including androgen receptor signaling inhibitors (ARSIs; e.g., abiraterone, enzalutamide, apalutamide, rezvilutamide, or darolutamide), chemotherapy, PARP inhibitors, radionuclide therapy, or other such treatments.
  • Short-term androgen deprivation therapy (ADT) and/or first-generation antiandrogen therapy prior to enrollment is permitted, provided that the interval from the first initiation of any such treatment to the date of enrollment does not exceed 3 months (≤12 weeks).
  • Expected survival >12 months.
  • Able to understand the study and voluntarily sign written informed consent.
  • Able and willing to comply with study visits and protocol procedures.
  • Willing to provide tumor tissue, blood, and other biological samples as required by the study protocol.
  • Absolute neutrophil count ≥1.5 × 10^9/L.
  • Platelet count ≥100 × 10^9/L.
  • Hemoglobin ≥90 g/L.
  • Total bilirubin ≤1.5 × upper limit of normal.
  • Alanine aminotransferase and aspartate aminotransferase ≤2.5 × upper limit of normal.
  • Serum albumin ≥20 g/L.
  • Serum creatinine ≤1.5 × upper limit of normal or creatinine clearance ≥50 mL/min.
  • Eastern Cooperative Oncology Group performance status ≤2.

Exclusion Criteria:

  • Current or prior history of another primary malignancy.
  • History of another malignancy within 3 years that differs from the study cancer in primary site or histology.
  • History of papillary thyroid carcinoma is allowed if it is well controlled.
  • History of basal cell carcinoma of the skin is allowed if it is well controlled.
  • History of squamous cell carcinoma of the skin is allowed if it is well controlled.
  • History of cervical carcinoma in situ is allowed if it is well controlled.
  • Prior radical prostatectomy.
  • Prior external beam radiotherapy.
  • Prior radical or ablative local therapy for prostate cancer.
  • Prior treatment with an androgen receptor signaling inhibitor, including abiraterone, enzalutamide, apalutamide, rezvilutamide, or darolutamide.
  • Prior chemotherapy for prostate cancer.
  • Major surgery within 4 weeks before enrollment.
  • Serious trauma within 4 weeks before enrollment.
  • Contraindication to radiotherapy.
  • Spinal cord compression.
  • Active enteritis.
  • Severe pelvic infection.
  • Inability to maintain the required body position for radiotherapy.
  • History of allergy to PET/CT tracer.
  • Nuclear medicine assessment showing super bone imaging.
  • Marked discordance between PSMA PET/CT and FDG PET/CT findings.
  • Disease progression during the 6-month run-in period of androgen deprivation therapy plus darolutamide before randomization.
  • Unacceptable toxicity during the 6-month run-in period of androgen deprivation therapy plus darolutamide before randomization.
  • No active tumor lesion on PSMA PET/CT after the 6-month run-in period.
  • Allergy to any component of the study treatment.
  • Active or poorly controlled serious infection.
  • Human immunodeficiency virus infection.
  • Acute or chronic active hepatitis B infection, defined as positive hepatitis B surface antigen with hepatitis B virus DNA >1 × 10^3/mL.
  • Acute or chronic active hepatitis C infection, defined as positive hepatitis C virus antibody with hepatitis C virus RNA >15 IU/mL.
  • Active pulmonary tuberculosis.
  • Other serious infectious disease.
  • New York Heart Association class III or IV congestive heart failure.
  • Persistent symptomatic arrhythmia.
  • Uncontrolled atrial fibrillation.
  • Left ventricular ejection fraction below the lower limit of normal on repeated echocardiographic assessments.
  • Uncontrolled hypertension, defined as systolic blood pressure ≥160 mmHg or diastolic blood pressure ≥100 mmHg.
  • Arterial thrombotic, embolic, or ischemic event within 6 months before enrollment.
  • Myocardial infarction within 6 months before enrollment.
  • Unstable angina within 6 months before enrollment.
  • Cerebrovascular accident within 6 months before enrollment.
  • Transient ischemic attack within 6 months before enrollment.
  • Medical condition requiring warfarin or coumarin anticoagulation therapy.
  • Uncontrolled hypercalcemia, defined as ionized calcium >1.5 mmol/L, total calcium >12 mg/dL, or corrected serum calcium above the upper limit of normal.
  • Symptomatic hypercalcemia requiring continuous bisphosphonate therapy.
  • Uncontrolled adrenal insufficiency.
  • History of abdominal fistula within 6 months before enrollment.
  • History of gastrointestinal perforation within 6 months before enrollment.
  • History of intra-abdominal abscess within 6 months before enrollment.
  • Severe non-healing wound.
  • Severe non-healing ulcer.
  • Gastrointestinal disease that may impair absorption.
  • Active peptic ulcer disease.
  • Uncontrolled nausea.
  • Uncontrolled vomiting.
  • Uncontrolled diarrhea.
  • History of small bowel resection that may impair drug absorption.
  • Other acute or chronic disease, psychiatric disorder, or laboratory abnormality that may increase the risk associated with study participation or study treatment.
  • Other acute or chronic disease, psychiatric disorder, or laboratory abnormality that may interfere with interpretation of study results.
  • Any other medical or psychological condition that, in the investigator's judgment, may affect participant safety, compliance, or study integrity.
  • Any condition that, in the investigator's judgment, makes the participant unsuitable for this study.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: PSMA PET/CT-Guided SBRT + Darolutamide + ADT
After a 6-month run-in period of darolutamide plus androgen deprivation therapy, eligible participants without disease progression and with residual PSMA PET/CT-positive active tumor lesions will receive PSMA PET/CT-guided stereotactic body radiotherapy to all active tumor lesions while continuing darolutamide plus androgen deprivation therapy.
Stereotactic body radiotherapy will be delivered in the experimental arm after the 6-month run-in period of darolutamide plus androgen deprivation therapy. Radiotherapy will target all residual PSMA PET/CT-positive active tumor lesions, while participants continue darolutamide plus androgen deprivation therapy. Target lesions may include active lesions in the prostate or prostate bed and metastatic sites. Dose and fractionation will be selected according to lesion location, lesion size, and organ-at-risk constraints as specified in the study protocol.
Darolutamide will be administered orally at 600 mg twice daily with food during the 6-month run-in period in combination with androgen deprivation therapy. After randomization, darolutamide will be continued in both treatment groups according to the assigned treatment strategy. Treatment may be interrupted or dose-reduced according to protocol-defined toxicity management rules.
Androgen deprivation therapy will be maintained throughout study treatment in both groups. The method of androgen deprivation therapy will be selected by the investigator according to the participant's clinical condition and may include surgical castration or medical castration with a luteinizing hormone-releasing hormone agonist or antagonist. Treatment will aim to maintain castrate testosterone levels according to the study protocol.
Aktiv komparator: Darolutamide + ADT
After a 6-month run-in period of darolutamide plus androgen deprivation therapy, eligible participants without disease progression and with residual PSMA PET/CT-positive active tumor lesions will continue darolutamide plus androgen deprivation therapy without local radiotherapy.
Darolutamide will be administered orally at 600 mg twice daily with food during the 6-month run-in period in combination with androgen deprivation therapy. After randomization, darolutamide will be continued in both treatment groups according to the assigned treatment strategy. Treatment may be interrupted or dose-reduced according to protocol-defined toxicity management rules.
Androgen deprivation therapy will be maintained throughout study treatment in both groups. The method of androgen deprivation therapy will be selected by the investigator according to the participant's clinical condition and may include surgical castration or medical castration with a luteinizing hormone-releasing hormone agonist or antagonist. Treatment will aim to maintain castrate testosterone levels according to the study protocol.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
3-Year Radiographic Progression-Free Survival (rPFS)
Tidsramme: From randomization to 3 years after randomization
Radiographic progression-free survival (rPFS) is defined as the time from randomization to radiographic disease progression or death from any cause, whichever occurs first. Progression is assessed using RECIST 1.1 for soft tissue and PCWG3 criteria for bone lesions. The 3-year rPFS rate will be estimated using the Kaplan-Meier method.
From randomization to 3 years after randomization

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Overall Radiographic Progression-Free Survival (o-rPFS)
Tidsramme: From first dose of induction therapy to radiographic progression or death, assessed up to 60 months
Overall radiographic progression-free survival is defined as the time from the first dose of induction therapy with darolutamide plus androgen deprivation therapy to the first occurrence of radiographic disease progression or death from any cause, whichever occurs first. Radiographic progression will be assessed according to RECIST 1.1 for soft-tissue lesions and PCWG3 criteria for bone lesions.
From first dose of induction therapy to radiographic progression or death, assessed up to 60 months
PSA Progression-Free Survival (PSA-PFS)
Tidsramme: From randomization to PSA progression or death, assessed up to 60 months
PSA progression-free survival is defined as the time from randomization to PSA progression per PCWG3 criteria or death from any cause, whichever occurs first. For participants with a PSA decline from baseline, PSA progression is defined as a ≥25% increase and an absolute increase of ≥2 ng/mL from the PSA nadir, confirmed by a second consecutive value obtained ≥3 weeks later. For participants without a PSA decline from baseline, PSA progression is defined as a ≥25% increase from baseline with an absolute increase of ≥2 ng/mL after 12 weeks of treatment.
From randomization to PSA progression or death, assessed up to 60 months
Time to Castration-Resistant Prostate Cancer (CRPC)
Tidsramme: From randomization to development of castration-resistant prostate cancer, assessed up to 60 months
Time to castration-resistant prostate cancer is defined as the time from randomization to the development of castration-resistant prostate cancer under castrate testosterone levels, defined as serum testosterone <50 ng/dL or <1.7 nmol/L. Castration-resistant prostate cancer is defined by biochemical progression, radiographic progression, or unequivocal clinical progression according to protocol-defined criteria.
From randomization to development of castration-resistant prostate cancer, assessed up to 60 months
Overall Survival (OS)
Tidsramme: From randomization to death from any cause, assessed up to 60 months
Overall survival is defined as the time from randomization to death from any cause.
From randomization to death from any cause, assessed up to 60 months
PSA Response Rate (≥50% Decline From Baseline)
Tidsramme: From randomization to PSA response, assessed up to 36 months
PSA response rate is defined as the proportion of participants who achieve a ≥50% decline in serum PSA from baseline (at randomization) at any time during treatment, confirmed by at least one repeat measurement approximately 4 weeks later.
From randomization to PSA response, assessed up to 36 months
Best Percent Change in PSA From Baseline
Tidsramme: From randomization up to 36 months
Best percent change in PSA from baseline is defined as the maximum percent decrease from baseline PSA at randomization to the lowest observed PSA value during follow-up.
From randomization up to 36 months
PSA Nadir
Tidsramme: From randomization up to 36 months
PSA nadir is defined as the lowest serum PSA value observed from randomization through the end of prespecified follow-up.
From randomization up to 36 months
Time to PSA Nadir
Tidsramme: From randomization up to 36 months
Time to PSA nadir is defined as the time from randomization to the date when the lowest serum PSA value is first observed.
From randomization up to 36 months
Incidence and Severity of Adverse Events
Tidsramme: From first study treatment to 30 days after the last study treatment or radiotherapy, whichever occurs later
Safety will be assessed by the incidence and severity of treatment-emergent adverse events, treatment-emergent serious adverse events, adverse events of special interest, darolutamide-related adverse events, adverse events leading to treatment discontinuation, and adverse events with fatal outcome. Adverse events will be graded according to CTCAE v6.0.
From first study treatment to 30 days after the last study treatment or radiotherapy, whichever occurs later
Quality of Life (EORTC QLQ-C30)
Tidsramme: Baseline at randomization and prespecified follow-up visits up to 36 months
Quality of life will be assessed using EORTC QLQ-C30 questionnaires. Scores and changes from baseline over time will be summarized and compared between treatment groups.
Baseline at randomization and prespecified follow-up visits up to 36 months
Quality of Life (QLQ-PR25)
Tidsramme: Baseline at randomization and prespecified follow-up visits up to 36 months
Quality of life will be assessed using EORTC QLQ-PR25 questionnaires. Scores and changes from baseline over time will be summarized and compared between treatment groups.
Baseline at randomization and prespecified follow-up visits up to 36 months
Quality of Life (EQ-5D)
Tidsramme: Baseline at randomization and prespecified follow-up visits up to 36 months
Quality of life will be assessed using EQ-5D questionnaires. Scores and changes from baseline over time will be summarized and compared between treatment groups.
Baseline at randomization and prespecified follow-up visits up to 36 months

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Samarbeidspartnere

Etterforskere

  • Hovedetterforsker: Hao Zeng, MD, PhD, West China Hospital

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

15. september 2026

Primær fullføring (Antatt)

1. august 2031

Studiet fullført (Antatt)

1. oktober 2031

Datoer for studieregistrering

Først innsendt

7. juni 2026

Først innsendt som oppfylte QC-kriteriene

14. juni 2026

Først lagt ut (Faktiske)

16. juni 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

10. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

6. september 2026

Sist bekreftet

1. april 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

UBESLUTTE

IPD-planbeskrivelse

Individual participant data (IPD) sharing has not been decided at this time. Any future sharing will be considered after study completion and publication, subject to IRB/ethics approval, applicable regulations, participant privacy protections, and data use agreements. Requests, if allowed, would require submission of a research proposal and will be evaluated by the study team.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

produkt produsert i og eksportert fra USA

Ja

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