Neoadjuvant Serplulimab in Combination With Chemotherapy in Locally Advanced Gastric or Gastro-esophageal Junction Cancer

Neoadjuvant Serplulimab in Combination With Chemotherapy in Locally Advanced Gastric or Gastro-esophageal Junction Cancer: a Single-arm Phase 2 Trial

evaluate efficacy and safety of neoadjuvant Serplulimab in Combination With Chemotherapy in Locally Advanced Gastric or Gastro-esophageal Junction Cancer

Study Overview

• Status: Recruiting
• Conditions: Gastric Adenocarcinoma
• Intervention / Treatment: Drug: Serplulimab+SOX

• Study Type: Interventional
• Enrollment (Estimated): 35
• Phase: Phase 2

Contacts and Locations

• Study Contact: Name: hongjie zhan; Phone Number: 18622228706; Email: hongjiezhan@163.com

Study Locations

• China
  • Tianjin, China
    • Recruiting
    • Tianjin Medical University Cancer Institute & Hospital
    • Contact: hongjie zhan, MD; Phone Number: 022-23109106; Email: hongjiezhan@163.com

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• histologically documented adenocarcinoma of Gastric or Gastroesophageal Junction. 2. clinically diagnosed stage T3-4aN+M0 according to ultrasound endoscopy or enhanced CT/MRI scan. 3. Male or female. Age ≥ 18 years and ≤75 years. 4. surgeons participating in this study consider the lesion a resectable one. 5. ECOG 0~1 6. Physical condition and adequate organ function to ensure the success of abdominal surgery. 7. Adequate hematological function: Neutrophil count ≥ 1.5 × 109/L, Platelets ≥ 100 × 109/L and Hemoglobin ≥90g/L. 8. Adequate liver function: Total bilirubin ≤ 1.5 × upper limit of normal (ULN); AST (SGOT) and ALT (SGPT) < 2.5 × ULN . ALP ≤ 2.5 × upper limit of normal (ULN); ALB ≥30g/L. 9. Adequate renal function: Serum creatinine ≤ 1.5 x ULN, and creatinine clearance ≥ 60 ml/min. 10. Adequate coagulation function: INR/PT≤ 1.5 x ULN, aPTT≤ 1.5 x ULN. 11. No serious concomitant disease that will threaten the survival of patients to less than 5 years. 12. Written (signed) informed consent. 13. Good compliance with the study procedures, including lab and auxiliary examination and treatment. 14. Female patients should not be pregnant or breast feeding. 15. PD-L1 assessment

Exclusion Criteria:

• patients with distant metastasis or unresectable primary lesion. 2. patients with T1, T2 lesion according to CT/MRI or ultrasound endoscopy. 3. history of chemo, radiation, immune therapy or radical resection for the GC/GEJ. 4. patients with active autoimmune disease or history of refractory autoimmune disease. 5. patients with active malignant tumor in recent 2 years, except the tumor studied in this research or cured locally tumor like resected basal cell or squamous cell skin cancer, superficial bladder cancer, cervical or breast carcinoma in situ. 6. uncontrollable pleural effusion, pericardial effusion, or ascites in 2 weeks before recruitment. 7. patients who have digestive tract bleeding in 2 weeks before recruitment or with high risk of bleeding. 8. perforation / fistula of GI tract in 6 months before recruitment. 9. patients with upper GI tract obstruction or functional abnormality or malabsorption syndrome, which can affect absorption of S-1. 10. losing over 20% body weight in 2 months before recruitment. 11. pulmonary disease history: interstitial pulmonary disease, non-infective pneumonitis, pulmonary fibrosis, acute pulmonary disease. 12. uncontrollable systemic diseases, including diabetes, hypertension, etc. 13. severe chronic or active infections in need of systemic antibacterial, antifungal, or antiviral treatment, including TB or HIV, etc. 14. patients with untreated chronic hepatitis B or HBV DNA over 500 IU/ml or positive HCV RNA. 15. patients with any cardiovascular risk factors below:

  1. cardiac chest pain occurring in 28 days before recruitment, defined as moderate pain that limits daily activity.
  2. pulmonary embolism with symptoms occurring in 28 days before recruitment.
  3. acute myocardial infarction occurring in 6 months before recruitment.
  4. any history of heart failure reaching grade 3/4 of NYHA in 6 months before recruitment.
  5. ventricular arrhythmias of Grade 2 or grater in 6 months before recruitment, or accompanied by supraventricular tachyarrhythmias requiring medical treatment.
  6. cerebrovascular accident within 6 months before recruitment. 16. patients with peripheral neuropathy NCI CTC AE grade 1, except those with only deep tendon reflex disappearing. 17. moderate or severe renal injury [creatinine clearance rate≤50 ml/min (according to Cockroft & Gault equation)], or Scr>1.5 x ULN. 18. dipyrimidine dehydrogenase (DPD) deficiency. 19. allergic to any drug in this study. 20. history of allogeneic stem cell transplantation or organ transplantation. 21. use of steroids (dosage>10mg/d prednisone) or other systemic immune suppressive therapy in 14 days before recruitment, except patients treated with regimens below: a. steroids for hormone replacement (dosage>10mg/d prednisone); b. steroids for local application with little systemic absorption; c. short -term (≤ 7 days) steroids for preventing allergy or vomiting. 22. vaccinated with live vaccine in 4 weeks before recruitment. 23. receiving immune (interleukin, interferon, thymin) treatment or treatment of other trials in 28 days before recruitment. 24. receiving palliative radiation in 14 days before recruitment. 25. history of anti PD-1, PD-L1, PD-L2 or any other specific T cell costimulation or checkpoint pathway targeted treatment. 26. receiving operation in 28 days before recruitment, only if the operation is a minimally invasive one e.g. PICC. 27. for patients with uncontrolled epilepsy, CNS diseases or history of mental disorder, researchers should evaluate whether their diseases will impede their signing of informed consent or compliance of treatment.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Neoadjuvant chemotherapy	Drug: Serplulimab+SOX; Serplulimab+Oxaliplatin+S1

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
PCR	Pathological complete regression rate	3 months after the last subject participating in

Collaborators and Investigators

• Sponsor: Tianjin Medical University Cancer Institute and Hospital

Study record dates

Study Major Dates

• Study Start (Actual): May 27, 2023
• Primary Completion (Estimated): December 30, 2024
• Study Completion (Estimated): December 31, 2024

Study Registration Dates

• First Submitted: July 4, 2024
• First Submitted That Met QC Criteria: July 4, 2024
• First Posted (Actual): July 11, 2024

Study Record Updates

• Last Update Posted (Actual): July 11, 2024
• Last Update Submitted That Met QC Criteria: July 4, 2024
• Last Verified: June 1, 2024

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Neoplasms by Histologic Type; Neoplasms; Carcinoma; Neoplasms, Glandular and Epithelial; Adenocarcinoma
• Other Study ID Numbers: HLX10IIT12-TJMUCH

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No