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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.

Aperçu de l'étude

Statut

Pas encore de recrutement

Les conditions

Type d'étude

Interventionnel

Inscription (Estimé)

200

Phase

  • Phase 2

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

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 d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur actif: Opération
surgery
Expérimental: 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.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Délai
2-year Disease-Free Survival (DFS) rate in the watchful waiting arm
Délai: 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

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
2-year Overall Survival (OS) in the watchful waiting arm
Délai: From randomization to death, up to 2 years
From randomization to death, up to 2 years
2-year OS in the surgery arm
Délai: From randomization to death, up to 2 years
From randomization to death, up to 2 years
R0 resection rate
Délai: Assessed at surgery
Assessed at surgery
Pathological Complete Response (pCR) rate
Délai: Assessed at surgery
Assessed at surgery
Major Pathological Response (MPR) rate
Délai: Assessed at surgery
Assessed at surgery
Event-Free Survival (EFS)
Délai: 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
Délai: 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
Délai: 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
Délai: 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)
Délai: 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.

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

1 juin 2026

Achèvement primaire (Estimé)

31 décembre 2027

Achèvement de l'étude (Estimé)

31 décembre 2028

Dates d'inscription aux études

Première soumission

9 avril 2026

Première soumission répondant aux critères de contrôle qualité

7 mai 2026

Première publication (Réel)

13 mai 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

13 mai 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

7 mai 2026

Dernière vérification

1 mars 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • NAT-ESCC-01

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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