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Active Not Recruiting NCT05602935

Efficacy and Safety of SOX Regimen Combined With Camrelizumab as Neoadjuvant Treatment in Locally Advanced Gastric Cancer: a Phase II, Single-arm Study

Conditions: Stomach Neoplasms, Digestive System Neoplasms, Neoplasms, Digestive System Diseases, Stomach Diseases, Neoplasms by Site

Sex: All
Ages: 18 Years – 75 Years
Phase: PHASE2
Enrollment: 30
Sponsor: The Second Affiliated Hospital of Fujian Medical University

Location: China

Summary

This is a single-arm, phase II study of camrelizumab combined with SOX regimen in subjects with resectable locally advanced gastric cancer. The patients will receive camrelizumab ,S-1 and oxaliplatin given every 3 weeks for 3 cycles as neoadjuvant therapy. After the surgery, adjuvant therapy which includes camrelizumab and SOX regimen will begin.

Eligibility Criteria

Inclusion Criteria:Aged 18-75 years, male or female;Histologically or cytological confirmed gastric adenocarcinoma;Without prior systematic therapy;The Eastern Cooperative Oncology Group Performance status (ECOG PS) 0-1;With measurable lesions according to Response Evaluation Criteria in Solid Tumors (RECIST) 1.1;Clinically diagnosed stage cT3-4bN0-3M0 evaluated by CT/MRI/EUS;Life expectancy of at least 3 months;Adequate function of blood, heart, liver, kidney and thyroid.Exclusion Criteria:History of immunodeficiency, including HIV positive, or other acquired or congenital immunodeficiency disease, or history of organ transplantation or allogeneic bone marrow transplantation;Unresectable tumor evaluated by investigator;Present of poorly controlled cardiac symptoms or disease, including but not limited to: (1) heart failure with NYHA class II or above (2) unstable angina, (3)myocardial infarction occurred within 1 year (4) clinical significance supraventricular or ventricular arrhythmias without clinical intervention or poorly controlled after clinical intervention;With tumors in other sites;History of any active autoimmune disease, including but not limited to: interstitial pneumonia, enteritis, hepatitis, hypohysitis, vasculitis, nephritis, hyperthyroidism, hypothyroidism (may be considered after hormone replacement therapy);Patients with psoriasis or childhood asthma/allergy who have been in complete remission and do not need any intervention as adults may be considered for inclusion, but patients requiring medical intervention with bronchodilators may not be included;Has a history of allergy to monoclonal antibody, any component of PD-1 Inhibitor, S-1 and oxaliplatin;With any mental illness;Pregnant or lactating women.

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05602935). StuddyBuddy aggregates publicly available trial information.