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NCT07595770RecruitingPhase 2

Adebrelimab Combined With Neoadjuvant Chemoradiotherapy for Esophageal Squamous Cell Carcinoma

A Study on the Safety and Efficacy of Adalimumab Combined With Chemoradiotherapy as Neoadjuvant Therapy for Esophageal Squamous Cell Carcinoma

Source: ClinicalTrials.gov · Last updated 19 May 2026

Brief summary (registry, in English)

This study aims to systematically evaluate the safety and efficacy of adalimumab combined with paclitaxel, carboplatin, and short-course radiotherapy in the neoadjuvant treatment of esophageal squamous cell carcinoma.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
37 (estimated)
First submitted
13 May 2026
Start date
22 May 2026
Primary completion date
1 Jan 2028
Lead sponsor
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
NCT number
NCT07595770

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 37
  • From 22 May 2026 to the primary completion date, 1 Jan 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • 1\. Patients who have received or are currently receiving chemotherapy, radiotherapy, immunotherapy, or targeted therapy
  • 2\. Patients with distant metastasis or inability to undergo resection after evaluation by thoracic surgeons
  • 5\. Patients with a history of autoimmune diseases who were receiving immunosuppressive therapy prior to enrollment, with immunosuppressive doses\>10 mg/day or oral prednisone for more than 2 weeks

Other illness

  • 6\. Severe allergy to immune preparations

Lab values

  • 4\. Severe impairment of heart, liver, and kidney function (heart function grade 3-4, ALT and/or AST exceeding the upper limit of normal by more than 1.5 times, Cr (serum creatinine) exceeding the upper limit of normal by more than 1.5 times)
  • 7\. Abnormal coagulation function: (PT\>16s, APTT\>53s, TT\>21s, Fib\<1.5 g/L), bleeding tendency or during thrombolytic or anticoagulant therapy

Other

  • 3\. Simultaneously developing tumors in other parts of the body
  • 8\. Pregnancy or lactation period
  • 9\. Other situations as judged by investigators not suitable for inclusion.;

Who the study is looking for

  • \- 1. Provided informed consent and sign the informed consent form;
  • 2\. Male or female, Aged 18-75 years (counted on the date of signing informed consent);
  • 3\. Pathological confirmed ESCC;
  • 4\. Patients assessed by thoracic oncologists as resectable without distant metastasis
  • 5\. Patients evaluate with clinical staging of T1-4aN1-3M0 or T3-4aN0M0(AJCC 9.0) based on imaging and pathological examination results;
  • 6\. Have at least one assessable lesion according to the RECIST V1.1
  • 7\. ECOG-PS score: 0-1;
  • 8\. Patients with normal function of organs such as heart, brain, lungs, and kidneys who can tolerate surgery;
  • 9\. With a life expectancy of ≥ 6 weeks;
  • 10\. Adequate major organ function without severe hematologic, cardiac, pulmonary, hepatic, renal, or bone marrow dysfunction, and no immunodeficiency disease;

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sun Yat Sen Memorial Hospital of Sun Yat sen University
Coordinator of this site? Confirm its status
GuangzhouChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.