Adebrelimab With Chemoradiotherapy and Surgery for G/GEJ

Jiangsu Cancer Hospital

Status and phase

Enrolling

Phase 2

Conditions

Gastroesophageal Adenocarcinoma

Gastric Adenocarcinoma

Treatments

Combination Product: Arm 1: Adebrelimab Combined with Chemoradiotherapy Followed by Surgery

Study type

Interventional

Funder types

Other

Identifiers

NCT06985602

GAS-Jiangsu03

Details and patient eligibility

About

Gastric cancer is one of the most common and deadly cancers globally, characterized by a poor prognosis. Approximately 70% of patients are diagnosed at an advanced stage, and the 5-year survival rate is only around 10%. While advancements in targeted therapies and immunotherapy have improved treatment efficacy and extended survival, advanced gastric and gastroesophageal junction adenocarcinomas remain incurable. Subgroup analyses indicate that patients with limited metastases, such as liver oligometastasis or retroperitoneal lymph node metastasis, may benefit more from conversion therapy. However, current guidelines do not recommend specific treatment protocols for gastric cancer with limited metastasis. Immunotherapy has shown moderate efficacy in selected patients with advanced gastric adenocarcinoma. Additionally, low-dose radiotherapy (LDRT) may synergistically enhance antitumor responses when combined with immunotherapy. This Phase II trial aims to evaluate the safety and efficacy of combining Adebrelimab, chemotherapy, and LDRT before surgery in treating adult patients with gastric or gastroesophageal junction adenocarcinoma.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Pathologically confirmed esophagogastric junction (EGJ)/gastric adenocarcinoma.
Patients with locally advanced disease (AJCC staging T4b or N2 fusion metastasis) or limited metastasis confirmed by endoscopy, CT, MRI, or PET/CT scans, and multidisciplinary team (MDT) discussion.
From a medical and surgical technical perspective, the primary lesion and surrounding abdominal lymph nodes are assessed as potentially resectable; limited metastatic lesions are evaluated by MDT for resectability or for the possibility of achieving curative treatment through other local treatment methods (such as local radiotherapy or radiofrequency ablation).
Exclusion of peritoneal metastasis.
Adequate hematological function: Neutrophil count ≥ 1.5 × 109/L, Platelets ≥ 100 × 109/L and Hemoglobin ≥90g/L.
Adequate liver function: Total bilirubin ≤ 1.5 × upper limit of normal (ULN); AST (SGOT) and ALT (SGPT) < 2.5 × ULN in the absence of liver metastases, or < 5 × ULN in case of liver metastases. ALP ≤ 2.5 × upper limit of normal (ULN); ALB ≥30g/L.
Adequate renal function: Serum creatinine ≤ 1.5 x ULN, and creatinine clearance ≥ 60 ml/min.
Adequate coagulation function: INR/PT≤ 1.5 x ULN, aPTT≤ 1.5 x ULN.
No serious concomitant disease that will threaten the survival of patients to less than 5 years.
Male or female. Age ≥ 18 years and ≤80 years.
Written (signed) informed consent.
Good compliance with the study procedures, including lab and auxiliary examination and treatment.
Female patients should not be pregnant or breast feeding.

Exclusion criteria

Non-adenocarcinoma histology of gastric/esophagogastric junction tumors, such as squamous cell carcinoma or neuroendocrine carcinoma.
The primary lesion is considered unresectable from a medical or surgical technical perspective.
Imaging diagnosis indicates widespread metastasis (metastasis that does not meet the criteria for limited metastasis as defined above is considered widespread metastasis).
Peripheral neuropathy of grade ≥2.
Poor nutritional status, BMI <18.5 kg/m², or PG-SGA score ≥9.
Underwent major surgery or suffered a severe injury within 4 weeks prior to the first dose of the investigational drug.
Presence of uncontrolled pleural effusion, pericardial effusion, or ascites requiring repeated drainage.
Received any investigational drug within 4 weeks prior to the first dose of the study drug.
Required systemic treatment with corticosteroids (daily >10 mg prednisone equivalent) or other immunosuppressive agents within 2 weeks prior to the first dose of the investigational drug.
Received an anti-tumor vaccine or live vaccine within 4 weeks before the first dose of the study drug.
Diagnosed with any active autoimmune disease or a history of autoimmune diseases.
History of immunodeficiency, including a positive HIV test, any acquired or congenital immunodeficiency diseases, or a history of organ transplantation or allogeneic bone marrow transplantation.
Any condition within 14 days prior to treatment requiring systemic corticosteroid therapy (dose>10mg/day of prednisone or equivalent) or other immunosuppressive treatments.
Presence of uncontrolled cardiac symptoms or conditions, such as:
- NYHA Class II or higher heart failure
- Unstable angina
- Myocardial infarction within the past year
- Clinically significant supraventricular or ventricular arrhythmias requiring clinical intervention.
Severe infection within 4 weeks prior to the first dose, including pneumonia requiring hospitalization, bacteremia, or infectious complications.
History of interstitial lung disease, non-infectious pneumonia, pulmonary fibrosis, or other uncontrolled acute pulmonary diseases.
Active pulmonary tuberculosis infection diagnosed by history or CT scan, or a history of active tuberculosis infection within the past year, or a history of untreated active tuberculosis infection more than one year ago.
Active hepatitis B or hepatitis C.
Laboratory abnormalities of sodium, potassium, or calcium greater than Grade 1 within 2 weeks before enrollment that cannot be corrected with treatment.
Known allergy to monoclonal antibodies, any PD-1 components, paclitaxel, capecitabine, or any components used in their formulations.
Pregnant or breastfeeding women, or women of childbearing potential who are unwilling or unable to use effective contraception.