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Trastuzumab Rezetecan and Adebrelimab, Alone or in Combination, After Chemoradiotherapy for HER2-Altered Unresectable Stage III Lung Cancer

17 de septiembre de 2026 actualizado por: Ming Chen

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

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

Intervencionista

Inscripción (Estimado)

105

Fase

  • Fase 2

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

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

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

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  1. Age ≥18 years.
  2. ECOG performance status 0-1.
  3. Histologically or cytologically confirmed Non-Small Cell Lung Cancer (NSCLC).
  4. Radiologically confirmed unresectable Stage III NSCLC per AJCC 9th edition.
  5. Pathologically confirmed HER2 mutation or HER2 overexpression (IHC 2+ or 3+).
  6. Life expectancy ≥3 months.
  7. 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.
  8. Total radiotherapy dose 60 Gy ± 10% (54-66 Gy) using IMRT (preferred) or 3D-CRT, with acceptable dosimetric constraints.
  9. Adequate organ and bone marrow function.
  10. 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.
  11. Signed informed consent form (ICF).

Exclusion Criteria:

  1. Known EGFR-activating mutations or ALK fusions.
  2. Presence of other driver gene mutations with approved targeted therapies available.
  3. Mixed SCLC and NSCLC, large cell neuroendocrine carcinoma, or sarcomatoid carcinoma.
  4. Prior treatment with HER2-targeted ADCs or HER2 TKIs.
  5. Malignant pleural effusion, pericardial effusion, or ascites.
  6. Participation in another clinical trial within 4 weeks or 5 half-lives prior to first dose.
  7. Systemic immunosuppressive therapy within 2 weeks prior to first dose.
  8. Known HIV infection.
  9. Active hepatitis B (HBsAg positive with detectable HBV-DNA and ALT > ULN) or active hepatitis C.
  10. Active autoimmune disease requiring systemic treatment.
  11. 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.
  12. 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.
  13. Significant cardiovascular disease.
  14. Severe infection within 4 weeks prior to first dose.
  15. Prior or planned allogeneic bone marrow or solid organ transplantation.
  16. Live attenuated vaccine within 28 days prior to first dose or planned during study. Pregnancy or breastfeeding.
  17. Known hypersensitivity to Adebrelimab, Trastuzumab Rezetecan, or any excipients.
  18. Known history of psychotropic substance abuse, alcohol abuse, or illicit drug use.
  19. Any condition that might impair the subject's ability to comply with study requirements.

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: 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

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

Patrocinador

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)

1 de septiembre de 2026

Finalización primaria (Estimado)

1 de diciembre de 2029

Finalización del estudio (Estimado)

1 de diciembre de 2031

Fechas de registro del estudio

Enviado por primera vez

13 de septiembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

17 de septiembre de 2026

Publicado por primera vez (Actual)

23 de septiembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

23 de septiembre de 2026

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

17 de septiembre de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

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.

No

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. .

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