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- Ensayo clínico NCT07836543
Trastuzumab Rezetecan and Adebrelimab, Alone or in Combination, After Chemoradiotherapy for HER2-Altered Unresectable Stage III Lung Cancer
A Randomized, Open-label, Multicenter, Phase II Study of Trastuzumab Rezetecan With Adebrelimab, Trastuzumab Rezetecan Alone and Adebrelimab Alone as Consolidation Therapy in Patients With Unresectable Stage III Non-Small Cell Lung Cancer Harboring HER2 Alterations Without Progression After Definitive Chemoradiotherapy
A randomized phase II study to assess the efficacy and safety of Trastuzumab Rezetecan and/or Adebrelimab as consolidation therapy following chemoradiotherapy in patients with unresectable stage III HER2-altered NSCLC.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
This is a randomized, open-label, multi-center phase II study evaluating the efficacy and safety of consolidation therapy with Trastuzumab Rezetecan combined with Adebrelimab versus Trastuzumab Rezetecan monotherapy versus Adebrelimab monotherapy in patients with unresectable stage III NSCLC harboring HER2 alterations (mutation or overexpression) who have not progressed after definitive concurrent or sequential chemoradiotherapy. Eligible patients will be randomized in a 1:1:1 ratio to receive either combination therapy, SHR-A1811 alone, or Adebrelimab alone for up to 12 months. The primary endpoint is progression-free survival (PFS) per RECIST v1.1.
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 2
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Ming Chen, MD
- Número de teléfono: +86 020-87345647
- Correo electrónico: chenming@sysucc.org.cn
Copia de seguridad de contactos de estudio
- Nombre: Chenfei Wu, MD
- Número de teléfono: +86 020-87345647
- Correo electrónico: wucf@sysucc.org.cn
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Age ≥18 years.
- ECOG performance status 0-1.
- Histologically or cytologically confirmed Non-Small Cell Lung Cancer (NSCLC).
- Radiologically confirmed unresectable Stage III NSCLC per AJCC 9th edition.
- Pathologically confirmed HER2 mutation or HER2 overexpression (IHC 2+ or 3+).
- Life expectancy ≥3 months.
- Completed at least two cycles of platinum-based chemotherapy (concurrent or sequential) with definitive radiotherapy. Consolidation chemotherapy after radiotherapy is not permitted; chemotherapy with or without immunotherapy before concurrent chemoradiotherapy is permitted.
- Total radiotherapy dose 60 Gy ± 10% (54-66 Gy) using IMRT (preferred) or 3D-CRT, with acceptable dosimetric constraints.
- Adequate organ and bone marrow function.
- Negative pregnancy test for women of childbearing potential within 7 days prior to first dose. Willing to use effective contraception during the study and for 180 days after the last dose.
- Signed informed consent form (ICF).
Exclusion Criteria:
- Known EGFR-activating mutations or ALK fusions.
- Presence of other driver gene mutations with approved targeted therapies available.
- Mixed SCLC and NSCLC, large cell neuroendocrine carcinoma, or sarcomatoid carcinoma.
- Prior treatment with HER2-targeted ADCs or HER2 TKIs.
- Malignant pleural effusion, pericardial effusion, or ascites.
- Participation in another clinical trial within 4 weeks or 5 half-lives prior to first dose.
- Systemic immunosuppressive therapy within 2 weeks prior to first dose.
- Known HIV infection.
- Active hepatitis B (HBsAg positive with detectable HBV-DNA and ALT > ULN) or active hepatitis C.
- Active autoimmune disease requiring systemic treatment.
- Other malignancies within 5 years, except adequately treated cervical carcinoma in situ, basal/squamous cell skin carcinoma, localized prostate cancer, or ductal carcinoma in situ.
- Active or history of Grade ≥2 radiation pneumonitis per RTOG/EORTC, or symptomatic interstitial lung disease. Participants with grade 2 radiation pneumonitis that resolves to grade 1 or lower within 14 days without systemic glucocorticoid treatment may undergo screening if the investigator considers there to be no risk of recurrence.
- Significant cardiovascular disease.
- Severe infection within 4 weeks prior to first dose.
- Prior or planned allogeneic bone marrow or solid organ transplantation.
- Live attenuated vaccine within 28 days prior to first dose or planned during study. Pregnancy or breastfeeding.
- Known hypersensitivity to Adebrelimab, Trastuzumab Rezetecan, or any excipients.
- Known history of psychotropic substance abuse, alcohol abuse, or illicit drug use.
- Any condition that might impair the subject's ability to comply with study requirements.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Arm A (Combination Therapy)
Drug: Trastuzumab Rezetecan + Adebrelimab |
Trastuzumab Rezetecan (4.8mg/kg, iv, d1, Q3W) and Adebrelimab (1200mg, iv, d1, Q3W). Treatment will continue for up to 12 months or until disease progression, unacceptable toxicity, or other criteria for treatment discontinuation are met. |
|
Experimental: Arm B (Targeted Monotherapy)
Drug: Trastuzumab Rezetecan |
Trastuzumab Rezetecan (4.8mg/kg, iv, d1, Q3W). Treatment will continue for up to 12 months or until disease progression, unacceptable toxicity, or other criteria for treatment discontinuation are met. |
|
Experimental: Arm C (Immunotherapy Monotherapy)
Drug: Adebrelimab |
Adebrelimab (1200mg, iv, d1, Q3W). Treatment will continue for up to 12 months or until disease progression, unacceptable toxicity, or other criteria for treatment discontinuation are met. |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Progression-Free Survival (PFS)
Periodo de tiempo: Assessed up to approximately 36 months.
|
Defined as the time from randomization to disease progression or death from any cause, whichever occurs first. |
Assessed up to approximately 36 months.
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Overall Survival (OS)
Periodo de tiempo: Assessed up to approximately 60 months.
|
Defined as the time from randomization to death from any cause. |
Assessed up to approximately 60 months.
|
|
Objective Response Rate (ORR)
Periodo de tiempo: Assessed up to approximately 36 months.
|
Defined as the proportion of participants whose best overall response (BOR) is complete response (CR) or partial response (PR), as assessed according to RECIST v1.1. |
Assessed up to approximately 36 months.
|
|
Duration of Response (DoR)
Periodo de tiempo: Assessed up to approximately 36 months.
|
Defined as the time from the first documented response (CR or PR) to the first documented disease progression (PD) or death from any cause, whichever occurs first. |
Assessed up to approximately 36 months.
|
|
Disease Control Rate (DCR)
Periodo de tiempo: Assessed up to approximately 36 months.
|
Defined as the proportion of participants who achieve complete response (CR), partial response (PR), or stable disease (SD) following treatment, as assessed according to RECIST v1.1. |
Assessed up to approximately 36 months.
|
|
Time to Death or Distant Metastasis (TTDM)
Periodo de tiempo: Assessed up to approximately 36 months.
|
Defined as the time from randomization to the first occurrence of distant metastasis or death from any cause. |
Assessed up to approximately 36 months.
|
|
Progression-Free Survival Rate at 6 Months
Periodo de tiempo: 6 months after randomization.
|
Kaplan-Meier estimate of the percentage of participants alive without disease progression at 6 months after randomization. |
6 months after randomization.
|
|
Progression-Free Survival Rate at 12 Months
Periodo de tiempo: 12 months after randomization.
|
Kaplan-Meier estimate of the percentage of participants alive without disease progression at 12 months after randomization. |
12 months after randomization.
|
|
Overall Survival Rate at 12 Months
Periodo de tiempo: 12 months after randomization.
|
Kaplan-Meier estimate of the percentage of participants alive at 12 months after randomization. |
12 months after randomization.
|
|
Overall Survival Rate at 24 Months
Periodo de tiempo: 24 months after randomization.
|
Kaplan-Meier estimate of the percentage of participants alive at 24 months after randomization. |
24 months after randomization.
|
|
Incidence of Adverse Events (AEs)
Periodo de tiempo: Assessed up to approximately 36 months.
|
AEs graded by CTCAE version 6.0 |
Assessed up to approximately 36 months.
|
Otras medidas de resultado
Medida de resultado |
Periodo de tiempo |
|---|---|
|
Patients reported disease-related symptoms and HRQoL by the EORTC QLQ-C30 questionnaires
Periodo de tiempo: Assessed up to approximately 36 months.
|
Assessed up to approximately 36 months.
|
|
Patients reported disease-related symptoms and HRQoL by the EORTC QLQ-LC13 questionnaires
Periodo de tiempo: Assessed up to approximately 36 months.
|
Assessed up to approximately 36 months.
|
Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- MA-NSCLC-II-064
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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