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Adebrelimab Plus Full-course Neoadjuvant Therapy for Resectable Locally Advanced ESCC (Phase 2) (NAT-ESCC-01)

A Prospective, Single-Center, Phase II Clinical Trial of Adebrelimab Combined With Full-Course Neoadjuvant Therapy for Watchful Waiting or Surgery in Patients With Resectable Locally Advanced Esophageal Squamous Cell Carcinoma

This is a prospective, single-center, randomized phase 2 study of adebrelimab plus full-course neoadjuvant therapy in resectable locally advanced esophageal squamous cell carcinoma. Patients achieving clinical complete response (cCR) after neoadjuvant treatment will be randomized 1:1 to watchful waiting with 2 cycles consolidation chemo-Immunotherapy or standard surgery. Primary endpoint is 2-year DFS. Secondary endpoints include OS, pCR/MPR, R0 resection rate, safety, and quality of life.

Descripción general del estudio

Estado

Aún no reclutando

Condiciones

Tipo de estudio

Intervencionista

Inscripción (Estimado)

200

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

  • Nombre: Peng Tang Peng Tang
  • Número de teléfono: +8618622228653
  • Correo electrónico: 18526812877@163.com

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:

  • Patients voluntarily participate in this study, sign an informed consent form, and demonstrate good compliance;
  • At least 18 years of age; gender is not restricted;
  • ECOG performance status: 0-1;
  • Patients with histologically confirmed resectable esophageal squamous cell carcinoma clinically staged as (T1N+M0 or T2-4aNanyM0);
  • No prior anticancer therapy for esophageal cancer, including chemotherapy, hormone therapy, radiation therapy, or immunotherapy;
  • Laboratory tests must meet the following criteria (within 7 days prior to baseline enrollment):

    1. Complete blood count (CBC):

      1. Hemoglobin (Hb) ≥ 90 g/L (no blood transfusion within the past 14 days);
      2. Neutrophil count (NEUT) ≥ 1.5 × 10⁹/L;
      3. Platelet count (PLT) ≥ 100 × 10⁹/L;
      4. White blood cell count (WBC) ≥ 3 × 10⁹/L;
    2. Biochemical Tests:

      1. Alanine transaminase (ALT) and aspartate transaminase (AST) ≤ 2.5×ULN;
      2. Serum total bilirubin (TBIL) ≤ 1.5×ULN;
      3. Serum creatinine (Cr) ≤ 1.5×ULN; (or creatinine clearance (CCr) ≥ 60 mL/min);
    3. Coagulation function: Activated partial thromboplastin time (APTT), International Normalized Ratio (INR), and prothrombin time (PT) ≤ 1.5×ULN;
    4. Thyroid function: Thyroid-stimulating hormone (TSH) ≤ ULN (if abnormal, FT3 and FT4 levels should also be evaluated; if FT3 and FT4 levels are normal, the patient may be enrolled);
    5. Doppler ultrasound assessment: Left ventricular ejection fraction (LVEF) ≥50%;
  • Female participants must agree to use contraceptive measures, such as an intrauterine device (IUD), oral contraceptives, or condoms, during the study and for 6 months after study completion; they must have a negative serum pregnancy test within 7 days prior to study enrollment and must not be breastfeeding; male participants must agree to use contraceptive measures during the study and for 6 months after study completion.

Exclusion Criteria:

  • Concurrent malignant neoplasms (except for cured basal cell carcinoma of the skin);
  • Diagnosis of cervical esophageal cancer;
  • History of severe hypersensitivity reactions following administration of other monoclonal antibodies;
  • Presence of any active autoimmune disease or history of autoimmune disease (such as, but not limited to: autoimmune hepatitis, interstitial pneumonia, enteritis, vasculitis, or nephritis; asthma requiring bronchodilators for medical intervention); however, the following patients are eligible for enrollment: vitiligo, psoriasis, or alopecia not requiring systemic treatment; well-controlled type 1 diabetes; hypothyroidism with normal thyroid function following replacement therapy;
  • Requiring immunosuppressants, or systemic or absorbable topical corticosteroids for immunosuppressive purposes (dose > 10 mg/day of prednisone or other corticosteroids of equivalent potency), and still using them within 2 weeks of the first dose;
  • Uncontrolled pleural effusion, pericardial effusion, or ascites requiring repeated drainage;
  • Uncontrolled symptoms of brain metastases, spinal cord compression, or carcinomatous meningitis occurring within 4 weeks prior to the first dose, or patients with brain or meningeal disease identified by CT or MRI at screening;
  • Patients with any severe and/or uncontrolled medical conditions, including:

    1. Acute or recurrent myocardial ischemia or myocardial infarction; poorly controlled and clinically significant arrhythmias; and heart failure of Class II or higher (New York Heart Association [NYHA] functional class); LVEF (left ventricular ejection fraction) < 50%;
    2. Active or uncontrolled severe infection (≥ Grade 2 CTC AE infection);
  • Receipt of a prophylactic or attenuated vaccine within 4 weeks prior to the first dose;
  • Other factors, as determined by the investigator, that may lead to forced discontinuation of the study, such as other serious illnesses (including psychiatric disorders) requiring concomitant treatment, severe laboratory abnormalities, or family or social factors that could compromise the subject's safety.
  • If HBsAg (+) and/or HBcAb (+), HBV DNA must be < 500 IU/mL (if the local center's lower limit of detection is higher than 500 IU/mL, the investigator may decide on enrollment based on specific circumstances) and the subject must continue to receive effective anti-HBV therapy during the study, or must have already started treatment with entecavir or tenofovir prior to study drug administration;
  • If HCV antibodies are positive, HCV-RNA testing must be performed; subjects with HCV-RNA > 10³ copies/mL must be excluded;
  • HIV-positive.

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
Comparador activo: Cirugía
surgery
Experimental: Combination therapy with chemotherapy and immunotherapy

Adebrelimab Injection,intravenous infusion, Day 1, every 3 weeks for 2 cycles. Albumin-bound paclitaxel 260 mg/m², carboplatin AUC = 5, intravenous infusion, Day 1, every 3 weeks for 2 cycles.

Two cycles of chemotherapy combined with immunotherapy.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
2-year Disease-Free Survival (DFS) rate in the watchful waiting arm
Periodo de tiempo: Assessed from randomization to disease recurrence, progression, or death, up to 2 years
Assessed from randomization to disease recurrence, progression, or death, up to 2 years

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
2-year Overall Survival (OS) in the watchful waiting arm
Periodo de tiempo: From randomization to death, up to 2 years
From randomization to death, up to 2 years
2-year OS in the surgery arm
Periodo de tiempo: From randomization to death, up to 2 years
From randomization to death, up to 2 years
R0 resection rate
Periodo de tiempo: Assessed at surgery
Assessed at surgery
Pathological Complete Response (pCR) rate
Periodo de tiempo: Assessed at surgery
Assessed at surgery
Major Pathological Response (MPR) rate
Periodo de tiempo: Assessed at surgery
Assessed at surgery
Event-Free Survival (EFS)
Periodo de tiempo: From enrollment to progression/recurrence/death, up to 2 years
From enrollment to progression/recurrence/death, up to 2 years
Clinical Complete Response (cCR) rate
Periodo de tiempo: Within 1-2 weeks prior to surgery, after completion of neoadjuvant therapy.
Assessed after completion of neoadjuvant therapy, prior to surgical resection.
Within 1-2 weeks prior to surgery, after completion of neoadjuvant therapy.
EORTC QLQ-C30 Quality of Life Score
Periodo de tiempo: Baseline, 6 months, 12 months, 24 months
Assessed using the European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire Core 30 (QLQ-C30). The scale ranges from 0 to 100, with higher scores indicating better quality of life for functional scales and worse symptoms for symptom scales.
Baseline, 6 months, 12 months, 24 months
Treatment Completion Rate
Periodo de tiempo: From first study treatment to end of neoadjuvant therapy,Evaluation period: up to 12 months.
The proportion of patients who complete the planned neoadjuvant therapy regimen as defined in the protocol.
From first study treatment to end of neoadjuvant therapy,Evaluation period: up to 12 months.
Adverse Event (AE) and Serious Adverse Event (SAE) Incidence (CTCAE v6.0)
Periodo de tiempo: From first study treatment to 30 days after last study treatment.
Incidence of all adverse events (AEs) and serious adverse events (SAEs) graded according to the Common Terminology Criteria for Adverse Events (CTCAE) version 6.0.
From first study treatment to 30 days after last study treatment.

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 junio de 2026

Finalización primaria (Estimado)

31 de diciembre de 2027

Finalización del estudio (Estimado)

31 de diciembre de 2028

Fechas de registro del estudio

Enviado por primera vez

9 de abril de 2026

Primero enviado que cumplió con los criterios de control de calidad

7 de mayo de 2026

Publicado por primera vez (Actual)

13 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

13 de mayo de 2026

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

7 de mayo de 2026

Última verificación

1 de marzo de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • NAT-ESCC-01

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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