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IL-18 Armored STEAP1 CAR T Cells for the Treatment of Metastatic Castration Resistant Prostate Cancer

28 août 2026 mis à jour par: Fred Hutchinson Cancer Center

Phase 1 Dose-Escalation and Expansion Study of IL-18 Armored STEAP1 CAR T in Participants With mCRPC

This phase I trial tests the safety, side effects, best dose and how well giving IL-18 armored STEAP1 CAR T cells after lymphodepleting chemotherapy (with cyclophosphamide and fludarabine) works for the treatment of castration resistant prostate cancer that has spread from where it first started (primary site) to other places in the body (metastatic). Giving chemotherapy, with cyclophosphamide and fludarabine, prior to CAR T cells helps kill cancer cells in the body and prepare the body to receive the CAR T cells. Chimeric antigen receptor (CAR) T-cell therapy is a type of treatment in which a patient's T cells (a type of immune system cell) are changed in the laboratory so they will attack cancer cells. T cells are taken from a patient's blood. Then the gene for a special receptor that binds to a certain protein on the patient's cancer cells is added to the T cells in the laboratory. The special receptor is called a chimeric antigen receptor. Large numbers of the CAR T cells are grown in the laboratory and given to the patient by infusion for treatment of certain cancers. Giving IL-18 armored STEAP1 CAR T cells after lymphodepleting chemotherapy may be safe, tolerable and/or effective in treating patients with metastatic castration resistant prostate cancer.

Aperçu de l'étude

Description détaillée

OUTLINE:

Patients undergo leukapheresis. Patients receive cyclophosphamide intravenously (IV) and fludarabine IV on days -5 to -3. Patients receive FH-STEAP1 IL-18 CAR T cell IV on day 0. Patients may continue to receive androgen deprivation therapy per standard of care, throughout the study. Patients undergo nuclear medicine bone scan, computed tomography (CT) scan, magnetic resonance imaging (MRI) and/or positron emission tomography (PET) scan, tumor biopsy and blood sample collection throughout the study. Patients may also undergo multigated acquisition (MUGA) scan or echocardiography during screening.

After completion of study treatment, patients are followed up on day +1, +3, +7, +10, +14, +21, + 28, months 2-6, month 9, month 12, then every 6 months until year 5 then yearly until year 15.

Type d'étude

Interventionnel

Inscription (Estimé)

20

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

    • Washington
      • Seattle, Washington, États-Unis, 98109
        • Fred Hutch/University of Washington Cancer Consortium
        • Contact:
        • Chercheur principal:
          • Rosa Nadal Rios, MD, PhD

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  • Documented, histologically confirmed adenocarcinoma of the prostate
  • Measurable disease by RECIST 1.1 criteria or bone only metastases with measurable PSA (≥ 1ng/mL)
  • Must have mCRPC with progressive disease (PD), stable disease (SD), lack of clinical benefit or intolerance to ≥ 1 line of systemic therapy, after becoming castration resistant
  • Have received the following for metastatic prostate cancer:

    • At least two lines of Food and Drug Administration (FDA)-approved therapies with at least one being a second-generation androgen receptor signaling inhibitor.
    • Targeted therapies for which they are eligible in the metastatic setting unless the patient has contraindications to receiving those medications, the agents are not available to the patient or the patient declines to receive these drugs due to personal preference
  • Castrate levels of testosterone (< 50 ng/dL) with or without the use of androgen deprivation therapy
  • 18 years or older at the time of enrollment
  • Capable of understanding and providing written informed consent
  • Fertile male participants and their female partners must be willing to use an effective contraceptive method before, during, and for at least 4 months after the FH-STEAP1 IL-18 CAR T cell infusion
  • Participants will be permitted to receive radiation therapy for palliative purposes throughout the study period, except during the 2-week period prior to undergoing leukapheresis
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • Serum creatinine ≤ 1.5 x upper limit of normal (ULN) or estimated creatinine clearance > 50 mL/min as calculated using the Cockcroft-Gault formula and not dialysis dependent
  • Total bilirubin ≤ 1.5 x ULN. Participants with suspected Gilbert syndrome may be included if total bilirubin (bili) > 3 mg/dL but no other evidence of hepatic dysfunction
  • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) < 5 x ULN
  • ≤ grade 1 dyspnea and oxygen saturation (SaO2) ≥ 92% on ambient air. If pulmonary function tests (PFTs) are performed based on the clinical judgement of the treating physician, participants with forced expiratory volume at 1 second (FEVI) ≥ 50% of predicted and carbon monoxide diffusing capability (DLCO) (adjusted for lung volume) of ≥ 40% of predicted will be eligible
  • All participants ≥ 60 years of age are required to have left ventricular ejection fraction (LVEF) evaluation performed within 1 year prior to lymphodepletion chemotherapy. LVEF may be established with an echocardiogram or MUGA scan, and left ejection fraction must be ≥ 45%
  • Absolute neutrophil count (ANC) > 1500 cells/ mm^3
  • Hemoglobin ≥ 9g g/dL
  • Platelets > 100,000 per mm^3

Exclusion Criteria:

  • Expecting to conceive or father children for the duration of the trial through 4 months after T cell infusion
  • Patients that require immediate therapy due to mass effect or spinal cord compression
  • Active autoimmune disease: Participants with active autoimmune disease requiring chronic immunosuppressive therapy are excluded. Case by case exemptions are possible with approval by principal investigator (PI)
  • Corticosteroid therapy at a dose equivalent of > 10 mg of prednisone per day (or equivalent). Pulsed corticosteroid use for disease control is acceptable
  • Concurrent use of other investigational anti-cancer agents except for androgen deprivation therapy
  • Uncontrolled concurrent illness: Participants may not have uncontrolled respiratory, endocrine, renal, gastrointestinal, genitourinary or systemic infection. There are exceptions to this criterion:

    • HIV positive participants on highly active antiretroviral therapy (HAART) with a CD4 count > 500 cells/mm^3 are considered controlled, as are individuals with a history of hepatitis C who have successfully completed antiviral therapy with an undetectable viral load, and those with hepatitis B who have hepatitis well controlled on medication;
    • Patients who have recent history of cerebrovascular accident, transient ischemic attack should be cleared by the neurology service before enrolling this study
    • Patients who have recent history of coronary artery disease or cardiac arrhythmia should be cleared by the cardiology service before enrolling this study. Case by case exemptions are possible with approval by PI
  • Participants with brain metastasis
  • Active treatment for prior immune related adverse event to any immunotherapy: Participants receiving ongoing treatment for prior serious immune-related adverse events are excluded, with exception of hormone supplementation or corticosteroid therapy at equivalent of > 10 mg prednisone (or equivalent) per day, unless otherwise approved by PI
  • Patients with a second malignancy in addition to their prostate cancer are not eligible if the second malignancy has required systemic treatment within the past 4 years or is not in complete remission. There are exceptions to this criterion: successfully treated non-metastatic basal cell and squamous cell skin carcinoma
  • Other medical, social, or psychiatric factor that interferes with medical appropriateness and/or ability to comply with study, as determined by the PI
  • Known allergic reactions to any of the components of study treatments
  • Participants who do not have a reasonable standard-of-care bridging therapy option available, as determined by the treating medical oncologist, to maintain disease control should clinically significant disease progression or worsening symptoms occur during the screening and T-cell manufacturing period

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: N / A
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Treatment (chemotherapy, FH-STEAP1 IL-18 CAR T cells)
Patients undergo leukapheresis. Patients receive cyclophosphamide intravenously (IV) and fludarabine IV on days -5 to -3. Patients receive FH-STEAP1 IL-18 CAR T cell IV on day 0. Patients may continue to receive androgen deprivation therapy per standard of care, throughout the study. Patients undergo nuclear medicine bone scan, CT scan, MRI and/or PET scan, tumor biopsy and blood sample collection throughout the study. Patients may also undergo MUGA scan or echocardiography during screening.
Passer une IRM
Autres noms:
  • IRM
  • Résonance magnétique
  • Balayage d'imagerie par résonance magnétique
  • Imagerie Médicale, Résonance Magnétique / Résonance Magnétique Nucléaire
  • M
  • Imagerie IRM
  • Imagerie RMN
  • NMRI
  • Imagerie par résonance magnétique nucléaire
  • Imagerie par résonance magnétique (IRM)
  • IRMs
  • Imagerie par résonance magnétique (procédure)
  • IRM structurelle
Subir une collecte d'échantillons de sang
Autres noms:
  • Collecte d'échantillons biologiques
  • Spécimen biologique collecté
  • Collecte de spécimens
  • Collection d'échantillons
Étant donné IV
Autres noms:
  • Cytoxane
  • CTX
  • (-)-Cyclophosphamide
  • 2H-1,3,2-Oxazaphosphorine, 2-[bis(2-chloroéthyl)amino]tétrahydro-, 2-oxyde, monohydraté
  • Carloxane
  • Ciclofosfamida
  • Ciclofosfamide
  • Cicloxal
  • Clafène
  • Clapène
  • CP monohydraté
  • CYCLO-cellule
  • Cycloblastine
  • Cyclophosphame
  • Cyclophosphamide monohydraté
  • Monohydrate de cyclophosphamide
  • Cyclophosphamide
  • Cyclophosphane
  • Cyclostine
  • Cytophosphane
  • Fosfaséron
  • Genoxal
  • Genuxal
  • Lédoxine
  • Mitoxane
  • Néosar
  • Revimmuniser
  • Syklofosfamide
  • WR-138719
  • Asta B 518
  • B-518
  • B518
  • WR 138719
  • WR138719
  • Frindovyx
Étant donné IV
Autres noms:
  • Fluradosa
Subir une leucaphérèse
Autres noms:
  • Leucocytophérèse
  • Leucophérèse thérapeutique
  • Aphérèse adsorbante des leucocytes
  • Aphérèse de réduction des globules blancs
Passer un PET scan
Autres noms:
  • Imagerie médicale, Tomographie par émission de positrons
  • ANIMAUX
  • TEP-scan
  • Scan de tomographie par émission de positrons
  • Tomographie par émission de positrons
  • PT
  • Tomographie par émission de positrons (procédure)
Passer un scanner
Autres noms:
  • TDM
  • CHAT
  • Scanner
  • Tomographie axiale informatisée
  • Tomographie assistée par ordinateur
  • Tomodensitométrie
  • tomographie
  • Tomographie axiale informatisée (procédure)
  • Tomodensitométrie (TDM)
  • Scan de chat diagnostique
  • Type de service de scan de chat diagnostique
Subir un scan MUGA
Autres noms:
  • Balayage du bassin sanguin
  • Angiographie à l'équilibre des radionucléides
  • Imagerie du pool sanguin contrôlé
  • MUGA
  • Ventriculographie des radionucléides
  • RNVG
  • Numérisation SYMA
  • Numérisation d'acquisition synchronisée à plusieurs portes
  • Numérisation MUGA
  • Balayage d'acquisition multi-portes
  • Balayage du ventriculogramme radionucléide
  • Balayage du pool cardiaque contrôlé
  • Analyse RNV
Subir une biopsie tumorale
Autres noms:
  • Bx
  • BIOPSIE_TYPE
Subir une échocardiographie
Autres noms:
  • Échocardiographie
  • CE
Given FH-STEAP1 IL-18 CAR T cells IV
Autres noms:
  • Monothérapie médicament
  • Traitement à un seul agent
  • Traitement de médicament unique
Receive standard of care androgen deprivation therapy
Autres noms:
  • ADT
  • Thérapie de privation androgénique
  • Thérapie anti-androgène
  • Traitement anti-androgène
  • Traitement antiandrogène
  • Thérapie de privation hormonale
Undergo nuclear medicine bone scan
Autres noms:
  • Scintigraphie osseuse

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Treatment-related unexpected grade 3 or higher toxicity
Délai: Up to 28 days post infusion
Up to 28 days post infusion
Incidence of adverse events
Délai: Up to 28 days post infusion
Up to 28 days post infusion
Prostate cancer response
Délai: Up to 1 year post infusion
Assessed by Prostate Cancer Working Group 3 (PCWG3) criteria.
Up to 1 year post infusion

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Progression free survival
Délai: From initiation of protocol treatment to disease progression or death of any cause, up to 1 year post infusion
Will be analyzed using Kaplan-Meier method and the results will be summarized by the median with a 95% confidence interval if appropriate.
From initiation of protocol treatment to disease progression or death of any cause, up to 1 year post infusion
Overall survival
Délai: From initiation of protocol treatment to death of any cause, up to 1 year post infusion
Will be analyzed using Kaplan-Meier method and the results will be summarized by the median with a 95% confidence interval if appropriate.
From initiation of protocol treatment to death of any cause, up to 1 year post infusion
Objective response rate
Délai: Up to 1 year post infusion
Defined as complete response or partial response by Response Evaluation Criteria in Solid Tumors 1.1 criteria and PCWG 3.
Up to 1 year post infusion
Stable disease
Délai: Up to 1 year post infusion
Assessed by RECIST 1.1 criteria and PCWG3.
Up to 1 year post infusion
Clinical benefit
Délai: Up to 1 year post infusion
Defined as overall response and stable disease assessed by RECIST 1.1 criteria and PCWG3.
Up to 1 year post infusion
Overall response
Délai: Up to 1 year post infusion
Assessed by immune RECIST criteria.
Up to 1 year post infusion
Prostate specific antigen (PSA) response
Délai: From baseline, up to 15 years
Defined as ≥ 50% reductions in PSA. The estimation with an exact 95% confidence interval will be provided.
From baseline, up to 15 years

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: Rosa Nadal Rios, MD, PhD, Fred Hutch/University of Washington Cancer Consortium

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

31 octobre 2026

Achèvement primaire (Estimé)

31 octobre 2030

Achèvement de l'étude (Estimé)

31 octobre 2044

Dates d'inscription aux études

Première soumission

28 août 2026

Première soumission répondant aux critères de contrôle qualité

28 août 2026

Première publication (Réel)

4 septembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

4 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

28 août 2026

Dernière vérification

1 août 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Oui

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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