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

28 de agosto de 2026 actualizado por: 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.

Descripción general del estudio

Estado

Aún no reclutando

Condiciones

Intervención / Tratamiento

Descripción detallada

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.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

20

Fase

  • Fase 1

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

    • Washington
      • Seattle, Washington, Estados Unidos, 98109
        • Fred Hutch/University of Washington Cancer Consortium
        • Contacto:
        • Investigador principal:
          • Rosa Nadal Rios, MD, PhD

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

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 de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: 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.
Someterse a una resonancia magnética
Otros nombres:
  • Resonancia magnética
  • Resonancia magnetica
  • Exploración de imágenes por resonancia magnética
  • Imágenes Médicas, Resonancia Magnética / Resonancia Magnética Nuclear
  • SRES
  • Imágenes de RM
  • Imágenes de RMN
  • RMN
  • Imágenes de resonancia magnética nuclear
  • Imágenes por resonancia magnética (IRM)
  • resonancia magnética nuclear
  • Imágenes por resonancia magnética (procedimiento)
  • Resonancias magnéticas
  • Resonancia magnética estructural
Someterse a la recolección de muestras de sangre
Otros nombres:
  • Recolección de muestras biológicas
  • Muestra biológica recolectada
  • Coleccion de especimenes
  • Recolección de muestras
Dado IV
Otros nombres:
  • Citoxano
  • CTX
  • (-)-ciclofosfamida
  • 2H-1,3,2-oxazafosforina, 2-[bis(2-cloroetil)amino]tetrahidro-, 2-óxido, monohidrato
  • Carloxano
  • Ciclofosfamida
  • Cicloxal
  • Clafen
  • Clafeno
  • CP monohidrato
  • Célula CYCLO
  • Cicloblastina
  • Ciclofosfano
  • Monohidrato de ciclofosfamida
  • Ciclostina
  • Citofosfano
  • Fosfaseron
  • Genoxal
  • Genuina
  • Ledoxina
  • Mitoxano
  • Neosar
  • Revimmune
  • Siklofosfamid
  • WR-138719
  • Asta B 518
  • B-518
  • B 518
  • B518
  • WR 138719
  • WR138719
  • Frindovyx
Dado IV
Otros nombres:
  • Fluradosa
Someterse a leucoféresis
Otros nombres:
  • Leucocitoféresis
  • Leucoféresis Terapéutica
  • Aféresis por adsorción de leucocitos
  • Aféresis para la reducción de glóbulos blancos
Someterse a una exploración PET
Otros nombres:
  • Imágenes médicas, tomografía por emisión de positrones
  • MASCOTA
  • Escaneo de mascotas
  • Tomografía por emisión de positrones
  • Tomografía de emisión de positrones
  • PT
  • Tomografía por emisión de positrones (procedimiento)
Someterse a una tomografía computarizada
Otros nombres:
  • Connecticut
  • GATO
  • Análisis de gato
  • Tomografía Axial Computarizada
  • Tomografía axial computarizada
  • Tomografía computarizada
  • tomografía
  • Tomografía axial computarizada (procedimiento)
  • Tomografía computarizada (TC)
  • Escaneo de gato de diagnóstico
  • Tipo de servicio de escaneo de gato de diagnóstico
Someterse a un escaneo MUGA
Otros nombres:
  • Exploración de la piscina de sangre
  • Angiografía con radionúclidos de equilibrio
  • Imagen de piscina de sangre cerrada
  • MUGA
  • Ventriculografía con radionúclidos
  • RNVG
  • Escaneo SIMA
  • Escaneo de adquisición sincronizado de múltiples puertas
  • Escaneo MUGA
  • Escaneo de adquisición de puertas múltiples
  • Exploración de ventriculograma con radionúclidos
  • Escaneo de grupo de corazón cerrado
  • Escaneo RNV
Someterse a biopsia tumoral
Otros nombres:
  • Caja
  • BIOPSIA_TIPO
Sufrir ecocardiografía
Otros nombres:
  • Ecocardiografía
  • CE
Given FH-STEAP1 IL-18 CAR T cells IV
Otros nombres:
  • Monoterapia con drogas
  • Tratamiento de agente único
  • Terapia de drogas individuales
Receive standard of care androgen deprivation therapy
Otros nombres:
  • ADT
  • Terapia de privación de andrógenos
  • Terapia antiandrogénica
  • Tratamiento Antiandrógeno
  • Terapia de privación hormonal
Undergo nuclear medicine bone scan
Otros nombres:
  • Gammagrafía ósea

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Treatment-related unexpected grade 3 or higher toxicity
Periodo de tiempo: Up to 28 days post infusion
Up to 28 days post infusion
Incidence of adverse events
Periodo de tiempo: Up to 28 days post infusion
Up to 28 days post infusion
Prostate cancer response
Periodo de tiempo: Up to 1 year post infusion
Assessed by Prostate Cancer Working Group 3 (PCWG3) criteria.
Up to 1 year post infusion

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Progression free survival
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: Up to 1 year post infusion
Assessed by RECIST 1.1 criteria and PCWG3.
Up to 1 year post infusion
Clinical benefit
Periodo de tiempo: 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
Periodo de tiempo: Up to 1 year post infusion
Assessed by immune RECIST criteria.
Up to 1 year post infusion
Prostate specific antigen (PSA) response
Periodo de tiempo: 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

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Colaboradores

Investigadores

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

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

31 de octubre de 2026

Finalización primaria (Estimado)

31 de octubre de 2030

Finalización del estudio (Estimado)

31 de octubre de 2044

Fechas de registro del estudio

Enviado por primera vez

28 de agosto de 2026

Primero enviado que cumplió con los criterios de control de calidad

28 de agosto de 2026

Publicado por primera vez (Actual)

4 de septiembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

4 de septiembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

28 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • RG1126433
  • NCI-2026-06012 (Identificador de registro: CTRP (Clinical Trial Reporting Program))
  • FH21226 (Otro identificador: Fred Hutch/University of Washington Cancer Consortium)

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

Sí

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .