Esta página se tradujo automáticamente y no se garantiza la precisión de la traducción. por favor refiérase a versión inglesa para un texto fuente.

Adebrelimab Combined With Chemoradiotherapy in Patients With Large Bulky Stage III Unresectable Non-Small Cell Lung Cancer

24 de abril de 2026 actualizado por: Zhijie Wang, Cancer Institute and Hospital, Chinese Academy of Medical Sciences

A Randomized Controlled Clinical Study of Adebrelimab Combined With Chemoradiotherapy in Patients With Large Bulky Stage III Unresectable Non-Small Cell Lung Cancer

This is a randomized, controlled, multicenter clinical study that enrolled patients with unresectable bulky stage III NSCLC, with PFS as the primary endpoint. The study aims to investigate the efficacy and safety of adebrelimab combined with chemoradiotherapy in the treatment of locally advanced/unresectable stage III non-small cell lung cancer.

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Estimado)

204

Fase

  • Fase 3

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

  • Nombre: Zhijie Wang, MD
  • Número de teléfono: +86 13466323860
  • Correo electrónico: jie_969@163.com

Ubicaciones de estudio

    • Beijing Municipality
      • Beijing, Beijing Municipality, Porcelana, 100021
        • National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

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:

  • Aged between 18 and 75 years;
  • ECOG performance status score of 0 or 1;
  • Histologically or cytologically confirmed non-small cell lung cancer (NSCLC);
  • Unresectable stage III NSCLC (per AJCC 9th edition staging), with primary tumor diameter T ≥ 5 cm or regional metastatic lymph node short-axis diameter N ≥ 2 cm;
  • Expected survival time of at least 3 months;
  • No prior anti-tumor treatment before enrollment, including radiotherapy, chemotherapy, surgery and targeted therapy;
  • Adequate function of major organs;
  • Female subjects must have a negative pregnancy test result and be willing to use effective contraception;
  • Subjects voluntarily participate in the study, sign the informed consent form, with good compliance and willingness to complete follow-up.

Exclusion Criteria:

  • Subjects with known positive EGFR mutation or positive ALK fusion.
  • Histologically or cytologically confirmed mixed SCLC and NSCLC, large cell neuroendocrine carcinoma, and sarcomatoid carcinoma.
  • Participation in another clinical trial within 4 weeks prior to the first study dose or within 5 half-lives of the study drug, whichever is shorter.
  • Subjects who have received systemic immunosuppressive therapy within 2 weeks before the first dose, or those who are expected to require systemic immunosuppressive drugs during the study treatment period.
  • Subjects with congenital or acquired immunodeficiency, such as HIV infection; or with a history of autoimmune diseases.
  • Active hepatitis B, hepatitis C, or co-infection with both hepatitis B and hepatitis C.
  • Uncontrolled third-space effusions, such as massive pleural effusion, ascites or pericardial effusion.
  • History of other malignant tumors (other than NSCLC) within 5 years prior to screening.
  • Subjects with prior interstitial lung disease requiring hormone therapy.
  • Subjects with severe cardiovascular and cerebrovascular diseases.
  • History of severe bleeding events or arterial/venous thromboembolic events.
  • Severe infection within 4 weeks before the first dose; evidence of active tuberculosis infection within 1 year prior to the first dose; active fungal, bacterial and/or viral infections requiring systemic treatment.
  • Subjects with prior or planned allogeneic bone marrow transplantation or solid organ transplantation.
  • History of live attenuated vaccination within 28 days before the first dose, or planned live attenuated vaccination during the study period; pregnant or lactating women; fertile patients who are unwilling or unable to adopt effective contraceptive measures.
  • Known hypersensitivity, anaphylactic reaction or intolerance to adebrelimab, chemotherapy agents, or their excipients.
  • Subjects with a known history of psychoactive substance abuse, alcoholism or drug addiction.

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: After chemoimmunotherapy induction followed by cCRT/sCRT, then maintenance immunotherapy.
Patients receive adebrelimab(1200 mg iv, q3w) combined with chemotherapy for 2 cycles of induction therapy, followed by sequential/concurrent chemoradiotherapy (sCRT/cCRT), and then undergo adebrelimab monotherapy for consolidation treatment.

Patients receive adebrelimab combined with chemotherapy for 2 cycles of induction therapy, followed by sequential/concurrent chemoradiotherapy (sCRT/cCRT), and then undergo adebrelimab monotherapy for consolidation treatment.

adebrelimab: 1200 mg iv, q3w Radiation therapy: Total dose of 60 Gy ± 10% (range: 54 Gy - 66 Gy). Chemotherapy: Regimens will be administered in accordance with guideline recommendations.

Subsequently, patients will receive adebrelimab monotherapy as consolidation treatment, with each treatment cycle lasting 3 weeks. Treatment will be continued until disease recurrence or metastasis, intolerable toxicity, subject's voluntary withdrawal, or investigator's decision to discontinue the subject from the study.

Comparador activo: Receive cCRT/sCRT followed by maintenance immunotherapy.
Adebrelimab monotherapy consolidation is administered after sCRT/cCRT.
Receive cCRT/sCRT followed by maintenance immunotherapy. adebrelimab: 1200 mg iv, q3w Radiation therapy: Total dose of 60 Gy ± 10% (range: 54 Gy - 66 Gy). Chemotherapy: Regimens will be administered in accordance with guideline recommendations. Subsequently, patients will receive adebrelimab monotherapy as consolidation treatment, with each treatment cycle lasting 3 weeks. Treatment will be continued until disease recurrence or metastasis, intolerable toxicity, subject's voluntary withdrawal, or investigator's decision to discontinue the subject from the study.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Progression-Free Survival (PFS)
Periodo de tiempo: From enrollment to the end of monitoring at 1.5 years.
PFS is defined as the time from the first dose of study treatment to the first documentation of disease progression according to RECIST v1.1 (as assessed by investigators) or death from any cause, whichever occurs first. Subjects who are alive without progression at the time of analysis will be censored at the date of the last tumor assessment.
From enrollment to the end of monitoring at 1.5 years.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Overall Survival (OS)
Periodo de tiempo: From enrollment to the end of monitoring at 1.5 years.
OS is defined as the time from the first dose of study treatment to death from any cause. Subjects who are alive at the time of analysis will be censored at the date of last follow-up.
From enrollment to the end of monitoring at 1.5 years.
Objective Response Rate (ORR)
Periodo de tiempo: From enrollment to the end of monitoring at 1.5 years.
ORR is defined as the proportion of subjects who achieve a complete response (CR) or partial response (PR) as per RECIST v1.1.
From enrollment to the end of monitoring at 1.5 years.
Duration of Response (DoR)
Periodo de tiempo: From enrollment to the end of monitoring at 1.5 years.
DoR is defined as the time from the first documentation of CR or PR to the first documentation of disease progression or death.
From enrollment to the end of monitoring at 1.5 years.
The incidence of adverse events
Periodo de tiempo: From enrollment to the end of monitoring at 1.5 years
Incidence, nature, and severity of adverse events (AEs), graded according to NCI-CTCAE v6.0, including immune-related AEs and serious AEs.
From enrollment to the end of monitoring at 1.5 years
Time to Death or Distant Metastasis(TTDM)
Periodo de tiempo: From enrollment to the end of monitoring at 1.5 years
From randomization/enrollment to the first occurrence of distant metastasis or death from any cause, whichever occurs first.
From enrollment to the end of monitoring at 1.5 years

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Incremental Cost-Utility Ratio (ICUR)
Periodo de tiempo: From randomization/enrollment to the end of 1.5-year follow-up.
The Incremental Cost-Utility Ratio (ICUR) is defined as the incremental total cost divided by the incremental quality-adjusted life years (QALYs) between the experimental treatment group and the control group. It reflects the additional cost required to gain one additional unit of health utility outcome (per QALY).
From randomization/enrollment to the end of 1.5-year follow-up.
Patient Quality of Life (QoL)
Periodo de tiempo: From baseline to the end of 1.5-year follow-up.
Patient Quality of Life (QoL) was assessed using validated patient-reported outcome questionnaires. Changes in health-related quality of life from baseline to scheduled follow-up time points were analyzed, including physical function, emotional function, social function and disease-related symptom domains.
From baseline to the end of 1.5-year follow-up.
Exploratory biomarker analysis
Periodo de tiempo: From enrollment to the end of 1.5-year follow-up.
Exploratory analysis of relevant biomarker characteristics and their correlation with clinical efficacy outcomes.
From enrollment to the end of 1.5-year follow-up.

Colaboradores e Investigadores

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

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 mayo de 2026

Finalización primaria (Estimado)

31 de diciembre de 2029

Finalización del estudio (Estimado)

31 de diciembre de 2030

Fechas de registro del estudio

Enviado por primera vez

24 de abril de 2026

Primero enviado que cumplió con los criterios de control de calidad

24 de abril de 2026

Publicado por primera vez (Actual)

1 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

1 de mayo de 2026

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

24 de abril de 2026

Última verificación

1 de abril 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. .

Suscribir