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Radium-223 for High-Volume Metastatic Hormone Sensitive Prostate Cancer (GUARD-QUANTUM)

16. Juli 2026 aktualisiert von: Alianza multidisciplinar para la investigación de los tumores genitourinarios -GUARD

Quantitative Unified Assessment of Novel Triplet Therapy and Unconventional Maintenance With Radium-223 for High-Volume Metastatic Hormone Sensitive Prostate Cancer: A Phase II Pilot Trial

GUARD-QUANTUM is a prospective, phase II, single-arm, non-randomized, non-blinded, investigator-initiated study. The rationale behind studying this combination lies in the potential additive or synergistic benefits that may arise from concurrently targeting androgen receptor signaling pathways and bone metastases.

Studienübersicht

Status

Noch keine Rekrutierung

Bedingungen

Intervention / Behandlung

Detaillierte Beschreibung

The trial will enroll competitively up to 50 patients with mHSPC and high volume disease (i.e. ≥4 bone metastatic foci in Tc-99m bone scanning, with at least one focus located outside the pelvis or vertebral bodies in the spine AND/OR visceral metastasis shown on computed tomography or magnetic resonance imaging not including lymph nodes). Patients should have started and be on treatment as per standard of care with first-line triplet therapy consisting of chemical or surgical androgen deprivation therapy (ADT), docetaxel and darolutamide. At least four cycles of docetaxel should have been administered and the last dosing of docetaxel be < 12 weeks prior the first planned dose of Ra223. Patients should have a good performance status (ECOG PS 0-2 and Charlson score ≤ 3) and have recovered from any prior toxicity from triplet therapy. Previous treatments other than chemotherapy for locoregional disease are acceptable.

Additionally to the IMPs and AXMPs, the study includes the administration of at least two doses of a bone protecting agent (zoledronic acid or denosumab) is required before the first administration of Ra223, and the bone protecting agent should have been started at least 6 weeks before the first administration of Ra223. Patients should also start treatment with vitamin D and calcium supplements

Studientyp

Interventionell

Einschreibung (Geschätzt)

50

Phase

  • Phase 2

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studienorte

  • Spanien
      • Barcelona, Spanien, 08036
        • Hospital Clinic de Barcelona
        • Kontakt:
        • Hauptermittler:
          • A Principal Investigator Designated by the Sponsor, M.D., Ph.D.
      • Barcelona, Spanien, 08041
        • Hospital Santa Creu i Sant Pau
        • Kontakt:
        • Hauptermittler:
          • A Principal Investigator Designated by the Sponsor, M.D., Ph.D.
      • Las Palmas de Gran Canaria, Spanien, 35016
        • Complejo Hospitalario Universitario Materno-Infantil de Gran Canaria (CHUIMI)
        • Kontakt:
        • Hauptermittler:
          • A Principal Investigator Designated by the Sponsor, M.D., Ph.D.
      • Madrid, Spanien, 28040
        • Hospital Clínico San Carlos
        • Kontakt:
        • Hauptermittler:
          • A Principal Investigator Designated by the Sponsor, M.D., Ph.D.
      • Madrid, Spanien, 28041
        • Hospital Universitario 12 de Octubre
        • Kontakt:
        • Hauptermittler:
          • A Principal Investigator Designated by the Sponsor, M.D., Ph.D.
      • Madrid, Spanien, 28046
        • Hospital Universitario La Paz
        • Kontakt:
        • Hauptermittler:
          • A Responsible Person Designated by the Sponsor, M.D., Ph.D.
      • Madrid, Spanien, 28050
        • Hospital Universitario HM Sanchinarro
        • Kontakt:
        • Hauptermittler:
          • A Principal Investigator Designated by the Sponsor, M.D., Ph.D.
      • Oviedo, Spanien, 33011
        • Hospital Universitario Central de Asturias (HUCA)
        • Kontakt:
        • Hauptermittler:
          • A Principal Investigator Designated by the Sponsor, M.D., Ph.D.
      • Santander, Spanien, 39008
        • Hospital Universitario Marques de Valdecilla
        • Kontakt:
        • Hauptermittler:
          • A Principal Investigator Designated by the Sponsor, M.D., Ph.D.
      • Santiago de Compostela, Spanien, 15706
        • Complejo Hospitalario Universitario de Santiago (CHUS)
        • Kontakt:
        • Hauptermittler:
          • A Principal Investigator Designated by the Sponsor, M.D., Ph.D.
      • Valencia, Spanien, 46009
        • Instituto Valenciano de Oncología (IVO)
        • Kontakt:
        • Hauptermittler:
          • A Principal Investigator designed by the Sponsor, M.D., Ph.D.
      • Valladolid, Spanien, 47003
        • Hospital Clínico Universitario de Valladolid (HCUV)
        • Kontakt:
        • Hauptermittler:
          • A Principal Investigator Designated by the Sponsor, M.D., Ph.D.

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

INCLUSION CRITERIA

Subjects must fulfill all of the following inclusion criteria to be eligible for enrollment to the study:

  1. Patients must be fully informed about the study and sign the informed consent form (ICF) before any study specific assessment.
  2. Patients ≥18 years old.
  3. ECOG performance status of 0 to 2 and Charlson score ≤ 3 prior to study entry, after docetaxel.
  4. Patients with histologically or cytologically confirmed diagnosis of prostate adenocarcinoma.

  5. Patients should have received triplet therapy with ADT (luteinizing hormone releasing hormone analogue (LHRHA) for continuous treatment or previous bilateral orchidectomy), docetaxel and darolutamide as first-line therapy for mHSPC. The following conditions apply:

    1. Received ≥ 4 cycles of docetaxel.
    2. Treatment with docetaxel should be finished ≤ 12 weeks before the first planned dose of Ra223.
    3. Having no progression of the disease after triplet therapy completion and before inclusion.

    Note: patients with prior therapies for locoregional disease are acceptable

  6. Patients should have recovered from any prior toxicity from ADT, darolutamide or docetaxel to CTCAE grade 1 or baseline levels.
  7. Presence of at least 4 bone metastasis on the screening bone scan, with or without lymph node and/or visceral metastases.
  8. Asymptomatic or mildly symptomatic (defined as short form question #3 in Brief Pain Inventory worst pain must be < 4).

  9. Patients should be willing to initiate or continue bisphosphonates /denosumab, calcium and vitamin D supplements (Section 7.4.4) prior to the first dose of Ra223.

    Note: Patients must start treatment with a bone protecting agent (at doses used to reduce the incidence of skeletal related events) before the time of signing the ICF. A minimum of two doses is recommended before the first administration of Ra223. The first administration of Ra223 should be scheduled at least 6 weeks after the first administration of the bone protecting agent.

  10. T-score ≥ -2.5 on a DXA scan done in the past 12 months. A DXA scan performed during the screening period will be encouraged but not mandated.

  11. Adequate organ and bone marrow function as follows (subject must not have received any growth factor within 4 weeks or a blood transfusion within 7 days of the hematology laboratory):

    1. Absolute neutrophil count (ANC) ≥ 1.5 x109/L;
    2. Platelets ≥ 100 x109/L;
    3. Hemoglobin ≥ 9.0 g/dl;
    4. Total bilirubin level ≤ 1.5 x institutional upper limit of normal (ULN), except for patients with Gilbert's disease ≤ 5.0 x ULN;
    5. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 x ULN;
    6. Creatinine ≤ 1.5 x ULN;
    7. CrCl < 30 mL/min;
    8. Albumin > 25 g/L.
  12. Participants who have pregnant partners must use a condom and those with partners of childbearing potential must use a condom and another adequate birth control measure if engaging in sexual activities during the study treatment period and for at least 1 week after last dose of darolutamide and 6 months after the last dose of Ra223. A highly effective method of birth control is defined as those which result in low failure rate (i.e., less than 1% per year) when used consistently and correctly.

EXCLUSION CRITERIA:

Subjects with any of the following could not enroll in this study:

  1. Presence of tumor lesion in central nervous system through radiologically confirmed diagnosis.
  2. Prior history of malignancies other than prostate adenocarcinoma (except patients with basal cell, squamous cell carcinoma of the skin, in-situ carcinoma or low-grade superficial bladder cancer, or the patient has been free of malignancy for a period of 3 years prior to inclusion).

  3. Patients experiencing progression during previous ADT or meeting criteria for castration resistant prostate cancer (CRPC).

    Note: Prior ADT is allowed.

  4. External irradiation, brachytherapy, or local treatment (including radiofrequency ablation, cryotherapy, high intensity focused ultrasound, etc.) within 4 weeks prior to the first dose of study treatment.
  5. Received prior chemotherapy for prostate cancer other than as part of first-line triplet therapy for mHSPC.
  6. Major surgery within 4 weeks prior to treatment.
  7. Prior hemibody external radiotherapy.
  8. Corticosteroids are allowed only at a dose ≤ 10 mg of prednisone (or equivalent) no matter the indication.

  9. Receiving abiraterone treatment as part of the first-line triplet therapy for mHSPC.

    Note: An increased risk of death and fractures was observed in a clinical study in which Ra223 was added to abiraterone acetate and prednisone/prednisolone in patients with asymptomatic or mildly symptomatic CRPC and this is the rationale to not include patients with this combination.

  10. Plan to receive any other antitumor therapies during this trial.
  11. Treatment with an investigational drug within the previous 4 weeks, or planned during the treatment period.

  12. Any other serious illness or medical condition such as, but not limited to:

    1. Any uncontrolled infection ≥ Grade 2 according to NCI-CTCAE v6.0;
    2. Gastrointestinal disorder affecting absorption (e.g., gastrectomy or active peptic ulcer disease);
    3. Crohn's disease or ulcerative colitis;
    4. Osteonecrosis of the jaw;
    5. Non-malignant bone disease with an osteoblastic activity;
    6. Bone marrow dysplasia;
    7. Fecal incontinence;
    8. Life-threatening illness unrelated to cancer.

  13. Significant cardiovascular disease including:

    1. Uncontrolled angina within 3 months prior to screening;
    2. Congestive heart failure New York Heart Association (NYHA) class III or IV, or patients with history of congestive heart failure NYHA class III or IV in the past, unless a screening echocardiogram or multi-gated acquisition scan (MUGA) performed within 3 months results in a left ventricular ejection fraction that is ≥ 45%. Of note, MUGA scans at baseline will not be mandated.
    3. History of clinically significant ventricular arrhythmias (e.g., ventricular tachycardia, ventricular fibrillation, torsades de pointes);
    4. History of Mobitz II second degree or third degree heart block without a permanent pacemaker in place;
    5. Uncontrolled hypertension as indicated by a resting systolic blood pressure > 160 millimeters of mercury (mm Hg) or diastolic blood pressure > 100 mm Hg at screening; Note: Initiation or adjustment of antihypertensive medication(s) is permitted prior to inclusion. Blood pressure must be re-assessed on two occasions that are separated by a minimum of 1 hour. The mean SBP / DBP values from each blood pressure assessment must be ≤ 160/100 mm Hg in order for a patient to be eligible for the study.
  14. Known hypersensitivity to any of the study drugs, study drug classes, or excipients in the formulation of the study drugs. No known hypersensitivity to Ra223 (refer to summary of product characteristics [SmPC]).
  15. Contraindication to both CT and MRI contrast agents.
  16. Contraindications for the use of bisphosphonates or denosumab as per physician judgment.
  17. Involvement in another therapeutic trial involving an experimental drug.
  18. Drug or alcohol abuse.
  19. Any medical condition that in the opinion of the investigator will negatively affect patients' clinical status when participating in this trial.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: N / A
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: QUANTUM intervention

Six intravenous administrations of Radium-223 chloride, in a dose of 55 kBq/kg body weight standard dose with a treatment interval between administrations of 4 weeks. Treatment with Ra223 could be prematurely discontinued in case of progression, unacceptable toxicity, withdrawal or death.

Patients received backgrount therapy with ADT and darolutamide
Arzneimittel: Ra223
Six intravenous administrations of Radium-223 chloride, in a dose of 55 kBq/kg body weight standard dose with a treatment interval between administrations of 4 weeks. Treatment with Ra223 could be prematurely discontinued in case of progression, unacceptable toxicity, withdrawal or death.
Arzneimittel: Darolutamide Oral Tablet
Darolutamide at 600 mg twice daily. Darolutamide administration will continue until progression, unacceptable toxicity, withdrawal or death, whichever comes first.
Sonstiges: Androgen Deprivation Therapy (ADT)
Standard of care ADT (surgical or drug). Administration will continue until progression, unacceptable toxicity, withdrawal or death, whichever comes first.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Treatment compliance
Zeitfenster: Throughout the study treatment period, approximately 6 months
Measured as the total number of cycles administered to each patient. Patients will be categorized in two groups, complete treatment compliance (complete ≥5 cycles of Ra223) and incomplete treatment compliance (complete <5 cycles of Ra223). The proportion of patients in each category and their 95% confidence interval (CI) calculated by Clopper-Pearson will be given.
Throughout the study treatment period, approximately 6 months

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Prostate-specific antigen (PSA) response rates
Zeitfenster: Throughout the study period, approximately 18 months
Response is defined as PSA <0.02 ng/mL at Ra223 completion. Rate of PSA response is defined as the number of subjects with absolute PSA response, divided by the total number of subjects evaluable for absolute PSA response (with high PSA levels at baseline).
Throughout the study period, approximately 18 months
Total alkaline phosphatase response rates
Zeitfenster: Throughout the study period, approximately 18 months
Defined as a reduction of ≥30% from the baseline value, before the first dose of study treatment (Ra223). The ALP response will be assessed only in patients with ALP increased levels at baseline. Percentage of patients who experience these reductions throughout the study period.
Throughout the study period, approximately 18 months
Radiographic progression-free survival (rPFS)
Zeitfenster: Throughout the study period, approximately 18 months
Defined from the day of first dose of Ra223 to the day the first event of radiological progression or death (due to any cause) is recorded. Assessed by investigator and defined as motivated by the recommendations of the Prostate Cancer Clinical Trials Working Group 3for the "delay/prevent" objective. rPFS will be estimated by Kaplan-Meier method. Patients who are alive without evidence of radiological progression at their last imaging assessment will be censored at that date.
Throughout the study period, approximately 18 months
Time to pain progression
Zeitfenster: Throughout the study period, approximately 18 months

Measured according to Brief Pain Inventory (BPI). Pain progression is defined in patients in the 'pain evaluable' population as:

an increase of 2 or more points in the BPI's "worst pain in 24 hours"-score from baseline observed at 2 consecutive evaluations ≥4 weeks apart, or initiation of short or long-acting opioid use for pain.

Time-to-pain progression is defined as the time (days) from the first dose of study treatment (Ra223) date, to the date of pain progression
Throughout the study period, approximately 18 months
Time to next systemic antineoplastic therapy
Zeitfenster: Throughout study period, approximately 18 months
This is the interval of time between first dose of study treatment (Ra223) and the first day of initiation of a next line of systemic antineoplastic therapy after the initial scheduled treatment.
Throughout study period, approximately 18 months
Time to castration resistance
Zeitfenster: Throughout the study period, approximately 18 months
Defined as the time to PSA progression (according to PCWG3 criteria is defined as the date that a 25% or greater increase and absolute increase of 2 ng/mL or more from the nadir [lowest at or after baseline] is documented, which both are confirmed by a second value obtained at least 3 weeks later, including all potential PSA values ≥2 ng/mL above nadir and ≥25% increase above nadir between initial assessment date and confirmation assessment date) with serum testosterone being at castrate level <0.50 ng/mL, or the time to progression by soft tissue lesions or bone lesions (as described above), whatever comes first.
Throughout the study period, approximately 18 months
Overall survival (OS)
Zeitfenster: Throughout the study period, approximately 18 months
Measured from the date of first dose of study treatment (Ra223) to the date of death whatever the cause of death. OS will be estimated by Kaplan-Meier method. Patients who are alive are censored at the date of the most recent follow-up examination.
Throughout the study period, approximately 18 months
Time to symptomatic skeletal event
Zeitfenster: Throughout the study period, approximately 18 months

Defined as the time elapsed between the day of first dose of study treatment administration (Ra223) to the day of symptomatic skeletal event recorded for each patient.

Symptomatic Skeletal-related events (SSEs) are defined as the first event of:

the first use of external-beam radiation therapy to relieve skeletal symptoms, new symptomatic pathologic vertebral or non-vertebral bone fractures, spinal cord compression, or tumor-related orthopedic surgical intervention.
Throughout the study period, approximately 18 months
Incidence of dose interruption
Zeitfenster: Throughout the study treatment period, approximately 6 months
Percentage of patients experiencing dose interruptions
Throughout the study treatment period, approximately 6 months
Health-related quality of life (HRQoL) through EQ-5D-5L
Zeitfenster: Throughout the study period, approximately 18 months

The EQ-5D-5L is a standardized, widely used questionnaire designed to measure a person's HRQoL. It evaluates overall health across five distinct dimensions (mobility, self-care, usual activities, pain/discomfort, anxiety/depression) and provides an actionable index score and a visual assessment of health status.

Here we will report the total score:

The top of the scale (100) represents "The best health you can imagine". The bottom of the scale (0) represents "The worst health you can imagine"
Throughout the study period, approximately 18 months
Health-related quality of life (HRQoL) through National Comprehensive Cancer Network Functional Assessment of Cancer Therapy - Prostate (FACT-P)
Zeitfenster: Throughout the study period, approximately 18 months

The FACT-P is a validated, multidimensional, patient-reported questionnaire used to evaluate the HRQOL of men diagnosed with prostate cancer. It is widely used by clinicians and researchers to track physical, emotional, and social well-being over time.

The assessment consists of 39 questions/statements graded on a 5-point Likert scale (ranging from 0 = "not at all" to 4 = "very much"). It is divided into five core domain: physical, social, emotional, functional and prostatic.

Here we will report the total score. The total FACT-P score ranges from 0 to 156. Higher scores represent a better health-related quality of life.
Throughout the study period, approximately 18 months

Andere Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Assessment of disease volume by novel imaging modalities (Prostate-Specific Membrane Antigen Positron Emission Tomography [PET-PSMA])
Zeitfenster: Throughout the study period, approximately 18 months
Patients will be assessed through PT-PSMA. The volume of disease will be reported trhough time. Best tumor size reduction will be reported
Throughout the study period, approximately 18 months
Biomarkers
Zeitfenster: Tumor archival tissue sample at baseline. Blood samples at baseline, within 7 days before end of Cycle 3 (each cycle is 28 days) and at disease progression
Transcriptome and whole genome sequencing to identify biomarkers that correlate with prognosis. Here we will report the most frequent genetic alterations and their prevalence in the study population. The analysis will be done in tumor and blood samples.
Tumor archival tissue sample at baseline. Blood samples at baseline, within 7 days before end of Cycle 3 (each cycle is 28 days) and at disease progression

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Alianza multidisciplinar para la investigación de los tumores genitourinarios -GUARD

Mitarbeiter

Bayer
MFAR

Ermittler

  • Studienstuhl: David Lorente, M.D., Ph.D., Instituto Valenciano de Oncologia
  • Studienstuhl: Guillermo de Velasco, M.D., Ph.D., Hospital Universitario 12 de Octubre

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. September 2026

Primärer Abschluss (Geschätzt)

1. Dezember 2029

Studienabschluss (Geschätzt)

1. Dezember 2029

Studienanmeldedaten

Zuerst eingereicht

2. Juli 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

16. Juli 2026

Zuerst gepostet (Tatsächlich)

21. Juli 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

21. Juli 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

16. Juli 2026

Zuletzt verifiziert

1. Juli 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Schlüsselwörter

Zusätzliche relevante MeSH-Bedingungen

Andere Studien-ID-Nummern

  • SC 2025-01 // 23161
  • 2026-525550-11-00 (Ctis)

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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    Prostatakrebs
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