- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT01028313
A Study of Panobinostat (LBH589) as Second-Line Therapy in Patients With Chronic Graft-Versus-Host Disease
A Phase II Study of Panobinostat (LBH589) as Second-Line Therapy in Patients With Chronic Graft-Versus-Host Disease
There is a clear need for effective, steroid-sparing agents for the management of chronic graft-versus-host disease (GVHD). Thus, agents like Histone deacetylase (HDAC) inhibitors, with the potential of decreasing pro-inflammatory events leading to GVHD without affecting graft-versus-leukemia (GVL), may have a central role in the prevention and treatment of GVHD.
This study will look at the efficacy of panobinostat (LBH589), an HDAC inhibitor, in the treatment of patients with chronic GVHD who have failed corticosteroids. In this group of patients, effective steroid-sparing options are limited and are usually associated with profound immunosuppression and decreased GVL effect.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Chronic GVHD is an autoimmune, inflammatory disorder that occurs in the majority of patients who experience acute GVHD. Long-term corticosteroids are still standard therapy for chronic GVHD. Corticosteroids are associated with high morbidity and non-relapse mortality. In addition, corticosteroids are broadly immunosuppressive and can also decrease the GVL effect and increase the incidence of relapse. There is a clear need for effective, steroid-sparing agents for the management of chronic GVHD. Thus, agents like HDAC inhibitors, with the potential of decreasing pro-inflammatory events leading to GVHD without affecting GVL, may have a central role in the prevention and treatment of GVHD.
This study will look at the efficacy of panobinostat (LBH589), an HDAC inhibitor, in the treatment of patients with chronic GVHD who have failed corticosteroids. In this group of patients, effective steroid-sparing options are limited and are usually associated with profound immunosuppression and decreased GVL effect.
Tipo de estudio
Fase
- Fase 2
Contactos y Ubicaciones
Ubicaciones de estudio
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Tennessee
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Nashville, Tennessee, Estados Unidos, 37023
- Tennessee Oncology, PLLC
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Chronic GvHD following allogeneic HSCT of any source (bone marrow, peripheral blood, or cord blood stem cells), from any donor type (related, unrelated, or mismatched) and with any type of malignancy. Chronic GvHD will be defined according to NIH Consensus Criteria.
Patients must have had inadequate response to treatment with steroids and calcineurin inhibitors. Patients must have been treated with an initial dose of at least 1 mg/kg/day of methylprednisolone (MP) or equivalent in combination with tacrolimus or cyclosporine and must fulfill the definition of steroid refractoriness or resistance. Steroid refractoriness or resistance will be defined as:
- Lack of any response after 1 month of treatment with MP, including 15 days of at least 0.5 mg/kg/day.
- Worsening of existing GvHD or new organ involvement at any time following one week of initiation of MP at 1 mg/kg/day.
- Reflare or worsening of GvHD at any time during steroid taper.
- Patients should not have received any drug or treatment for chronic GvHD other than steroids and calcineurin inhibitors (i.e., cyclosporine or tacrolimus).
- Patient must not have evidence of primary disease relapse.
- An ECOG (Eastern Cooperative Oncology Group) performance status of ≤2
- Baseline MUGA or ECHO must demonstrate left ventricular ejection fraction (LVEF) ≥40%.
- No uncontrolled arrhythmias or symptoms of heart disease.
- FEV1, FVC, and DLCO ≥40%.
Laboratory values as follows:
- white blood cell ≥2500/mm³;
- absolute neutrophil count (ANC) ≥1,000/mm³;
- hemoglobin ≥9.5 g%;
- platelets ≥50,000/mm³;
- total bilirubin <3 x upper limits of normal;
- aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤5 × the institutional upper limit of normal (ULN);
- creatinine <1.5 × ULN or creatinine clearance ≥ 50 ml/min;
- serum potassium ≥ LLN;
- serum sodium ≥ LLN;
- serum calcium WNL;
- serum phosphorus WNL;
- serum magnesium WNL;
- Patients with elevated alkaline phosphatase due to bone metastasis may be enrolled.
- TSH and free T4 within normal limits (clinically euthyroid patients are permitted to receive thyroid supplements to treat underlying hypothyroidism).
- Age ≥ 18 years, male or female.
- Ability to understand and willingness to sign a written informed consent document.
Exclusion Criteria:
- Prior HDAC, DAC, HSP90 inhibitors or valproic acid for the treatment of cancer.
- Patients who will need valproic acid for any medical condition during the study or ≤5 days prior to first panobinostat treatment.
- Use of prior immunosuppressants other than steroids and calcineurin inhibitors(i.e. cyclosporine or tacrolimus).
- Chronic active hepatitis or cirrhosis.
Impaired cardiac function including any of the following:
- Patients with congenital long QT syndrome;
- Patients with history or presence of sustained ventricular tachyarrhythmias;
- Patients with any history of ventricular fibrillation or Torsades de Pointes;
- Patients with bradycardia defined as HR <50 bpm. Patients with pacemakers are eligible if HR ≥50 bpm.
- Patients with myocardial infarction or unstable angina ≤6 months prior to starting study drug;
- Right bundle branch block plus left anterior hemiblock (bifasicular block);
- Screening ECG with QTc >450 msec;
- Congestive heart failure (CHF) > New York Heart Association (NYHA) Class II (see Appendix D).
- Concomitant use of drugs with a risk of causing Torsades de Pointes (see Appendix A).
- Other concurrent severe and/or uncontrolled medical conditions.
- Any condition that impairs patient's ability to swallow whole pills or gastrointestinal (GI) tract disease that involves an inability to take oral medication, malabsorption syndrome, a requirement for intravenous (IV)
Plan de estudios
¿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 |
|---|---|
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Experimental: 1
Systemic Therapy
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20 mg PO three times weekly
Otros nombres:
1 mg/kg/day PO continuously
Otros nombres:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
|---|---|
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To assess the response rate to panobinostat of patients with cGvHD inadequately treated with steroids and calcineurin inhibitors.
Periodo de tiempo: 30 months
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30 months
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Medidas de resultado secundarias
Medida de resultado |
Periodo de tiempo |
|---|---|
|
To evaluate the safety and tolerability of panobinostat in patients with cGvHD.
Periodo de tiempo: 30 months
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30 months
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To assess the steroid-sparing capacity of panobinostat (as proportion of patients able to discontinue steroids while receiving, or following therapy with, panobinostat).
Periodo de tiempo: 30 months
|
30 months
|
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To assess changes in quality of life (QOL) after treatment with panobinostat.
Periodo de tiempo: 30 months
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30 months
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To analyze survival at 6 and 12 months after initiation of panobinostat.
Periodo de tiempo: 30 months
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30 months
|
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To evaluate the relapse rate of the underlying malignancy as well as the occurrence of second malignancies at 6 and 12 months after initiation of panobinostat.
Periodo de tiempo: 30 months
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30 months
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Silla de estudio: Daniel R Couriel, M.D., SCRI Development Innovations, LLC
Fechas de registro del estudio
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Enfermedades del sistema inmunológico
- Enfermedad de injerto contra huésped
- Efectos fisiológicos de las drogas
- Mecanismos moleculares de acción farmacológica
- Agentes Autonómicos
- Agentes del sistema nervioso periférico
- Inhibidores de enzimas
- Agentes antiinflamatorios
- Agentes antineoplásicos
- Antieméticos
- Agentes Gastrointestinales
- Glucocorticoides
- Hormonas
- Hormonas, sustitutos hormonales y antagonistas hormonales
- Agentes Antineoplásicos Hormonales
- Agentes neuroprotectores
- Agentes Protectores
- Inhibidores de histona desacetilasa
- Prednisolona
- Acetato de metilprednisolona
- Metilprednisolona
- Hemisuccinato de metilprednisolona
- Acetato de prednisolona
- Hemisuccinato de prednisolona
- Fosfato de prednisolona
- Panobinostat
Otros números de identificación del estudio
- SCRI BMT 02
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