SHR2554 Plus Liposomal Mitoxantrone as First-line Treatment for Peripheral T-cell Lymphoma (PTCL)
An Open-label, Multicenter, Phase Ib/II Exploratory Clinical Study of EZH2 Inhibitor SHR2554 in Combination With Liposomal Mitoxantrone for the First-line Treatment of Peripheral T-cell Lymphoma
Descripción general del estudio
Estado
Estado
Condiciones
Condiciones
Intervención / Tratamiento
Intervención / Tratamiento
Tipo de estudio
Tipo de estudio
Inscripción (Estimado)
Inscripción
Fase
Fase
- Fase 2
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
Estudio Contacto
- Nombre: Liang Huang
- Número de teléfono: +86 022-23608126
- Correo electrónico: huangliang@ihcams.ac.cn
Criterios de participación
Criterio de elegibilidad
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Age ≥18 years old,regardless of gender;
- Centrally confirmed histopathological/cytologic diagnosis of PTCL with the following subtypes:Peripheral T-cell lymphoma, not otherwise specified (PTCL, NOS);Follicular helper T (TFH) cell lymphoma of lymph nodes, including angioimmunoblastic, follicular, NOS; Enteropathy-associated T-cell lymphoma(EATL); Monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL)and any other PTCL subtypes deemed by the investigator to be eligible for inclusion.
- No prior anti-tumor therapy.
- There must be at least one measurable or evaluable lesion that meets the Lugano 2014 criteria for lymphoma: Measurable lesion: Nodal lesions with major diameter greater than 1.5cm and minor diameter greater than 1.0cm as assessed by PET/CT or Computed Tomography (CT) and/or Magnetic Resonance Imaging (MRI); Or the length of extranodal lesions >1.0cm; 2)Evaluable lesions: PET-CT showed increased uptake in lymph nodes or extranodal regions (higher than liver) and imaging features consistent with lymphoma;
- ECOG performance status score: 0-2;
- Expected survival time ≥3 months;
- Have adequate organ and bone marrow functiont;
- No concurrent hemophagocytic lymphohistiocytosis (HLH). If a patient has clinically diagnosed HLH, enrollment eligibility will be determined by the investigator based on an evaluation of the patient's general physical condition following targeted anti-HLH therapy.
- Women of childbearing potential must have a negative serum pregnancy test within 7 days before the first dose of medication; Effective contraception should be used from the time of informed consent until 6 months after the last dose of study drug.
- Capable of understanding the study procedures and voluntarily signing a written informed consent form (ICF).;
Exclusion Criteria:
- Prior treatment with epigenetic agents before enrollment;
- Patients with a history of severe cardiac disease, history of radiation therapy to the mediastinal/pericardial region, cumulative anthracycline dose > 550 mg (doxorubicin equivalent), prior use of mitoxantrone, baseline left ventricular ejection fraction (LVEF) < 50%, or history of exposure to other cardiotoxic drugs;
- History of other primary aggressive malignancies that are not in remission, or have been in remission for less than 3 years;
- Primary central nervous system (CNS) lymphoma or secondary CNS involvement.
- Known allergy or hypersensitivity to the study drugs or their related metabolites;
- Currently participating in another clinical study, or less than 4 weeks elapsed from the end of treatment in a previous clinical study to the planned start of study treatment;
- Pregnant or lactating women;
- Active infections;
- Medical History and Concurrent Conditions;
- History of Human Immunodeficiency Virus (HIV) infection and/or Acquired Immunodeficiency Syndrome (AIDS);
- Patients with mental disorders or those unable to provide informed consent
- Any other condition deemed by the investigator to be unsuitable for study enrollment;
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)
Número de brazos
Armas e Intervenciones
Grupo de participantes/brazoGrupo de participantes/brazo |
Intervención / TratamientoIntervención / Tratamiento |
|---|---|
|
Experimental: SHR2554 combined with Liposomal Mitoxantrone
|
Patients will receive 6 cycles of SHR2554 combined with liposomal mitoxantrone as induction therapy.
All patients who achieve a complete response (CR) after induction therapy are eligible for transplantation.
Patients achieving CR or partial response (PR), as well as those post-transplantation, may receive SHR2554 maintenance therapy in 28-day cycles.
Maintenance therapy will continue until disease progression or other reasons for discontinuation.
The maximum duration of SHR2554 administration in the maintenance phase will not exceed 24 months.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Incidence of Dose-Limiting Toxicities (DLT)
Periodo de tiempo: Cycle 1 (28 days)
|
Adverse events (AE) defined as DLT events per protocol
|
Cycle 1 (28 days)
|
|
Complete response (CR) rate
Periodo de tiempo: up to 6 months after enrollment
|
The proportion of subjects evaluated as complete response (CR) according to Lugano 2014 efficacy evaluation criteria
|
up to 6 months after enrollment
|
Medidas de resultado secundarias
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Adverse events(AE)
Periodo de tiempo: From the first day of medication to 28 days after the last dose
|
The safety of the drug was evaluated by NCI-CTC AE 6.0 standard.
Hematologic and non-hematologic toxicity.
|
From the first day of medication to 28 days after the last dose
|
|
Objective response rate (ORR)
Periodo de tiempo: up to 6 months after enrollment
|
The proportion of subjects evaluated as complete response (CR) and partial response (PR) according to Lugano 2014 efficacy evaluation criteria
|
up to 6 months after enrollment
|
|
Duration of Response (DOR)
Periodo de tiempo: up to 2.5 years post first treatment
|
The time from the first assessment of CR/PR to the first assessment of PD or death from any cause in the subject
|
up to 2.5 years post first treatment
|
|
Duration of complete response (CR)
Periodo de tiempo: up to 2.5 years post first treatment
|
The time from the first assessment of CR to the first assessment of PD or death from any cause in the subject
|
up to 2.5 years post first treatment
|
|
Progression-free Survival (PFS)
Periodo de tiempo: Up to 2.5 years
|
From the time subjects were enrolled to the time of disease progression (in any way) or death from any cause.
|
Up to 2.5 years
|
|
Overall survival (OS)
Periodo de tiempo: Up to 2.5 years
|
From the date of inclusion to date of death, irrespective of cause.
|
Up to 2.5 years
|
Colaboradores e Investigadores
Patrocinador
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Inicio del estudio
Finalización primaria (Estimado)
Finalización primaria
Finalización del estudio (Estimado)
Finalización del estudio
Fechas de registro del estudio
Enviado por primera vez
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Publicado por primera vez
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización publicada
Última actualización enviada que cumplió con los criterios de control de calidad
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Otros números de identificación del estudio
Otros números de identificación del estudio
- IIT2026083
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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