[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hepatic-metastasis-of-pancreatic-cancer\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hepatic-metastasis-of-pancreatic-cancer":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":5},"100631729","phase-2-hepatic-arterial-infusion-of-sodium-bicarbonate-nahco3-combined-with-nasox-regimen-and-programmed-death-1-pd-1-inhibitors-for-pancreatic-cancer-liver-metastases-100631729",false,"NCT07504471","Hepatic Arterial Infusion of Sodium Bicarbonate (NaHCO3) Combined With NASOX Regimen and Programmed Death-1 (PD-1) Inhibitors for Pancreatic Cancer Liver Metastases","A Prospective, Single-Center, Phase II Clinical Study of Hepatic Arterial Infusion of Sodium Bicarbonate (NaHCO3) Combined With NASOX Regimen (Liposomal Irinotecan, Oxaliplatin, and S-1) Hepatic Arterial Infusion Chemotherapy (HAIC) and Intra-Arterial Programmed Death-1 (PD-1) Inhibitors for Liver Metastases From Pancreatic Cancer","Inclusion Criteria:\n\n* Aged 18 years and above, with no gender restrictions;\n* Pathologically confirmed pancreatic cancer (originating from the pancreatic ductal epithelium), with metastasis to the liver;\n* Eastern Cooperative Oncology Group (ECOG) performance status score of 0 to 2;\n* Adequate organ function, meeting the following criteria:\n\n  a. Hematological tests:\n  1. Neutrophils ≥ 1.5 × 10⁹ \u002FL;\n  2. White blood cells ≥ 3.0 × 10⁹ \u002FL;\n  3. Platelets ≥ 85 × 10⁹ \u002FL;\n  4. Hemoglobin ≥ 70 g\u002FL; b. Biochemical tests:\n\n  \u003C!-- -->\n\n  1. Total bilirubin ≤ 2× upper limit of normal (ULN) (for subjects with biliary obstruction, after biliary drainage ≤ 2.5 × ULN);\n  2. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) in metastatic subjects ≤ 5 × ULN;\n  3. Albumin level ≥ 28 g\u002FL;\n  4. Creatinine clearance rate ≥ 60 ml\u002Fmin; c. Cardiac function tests:\n\n  \u003C!-- -->\n\n  1. Normal electrocardiogram (ECG) or ECG abnormalities deemed clinically insignificant by the investigator;\n  2. Left ventricular ejection fraction (LVEF) ≥ lower limit of normal;\n* At least 3 weeks post-surgery, radiotherapy, chemotherapy, or other anti-tumor treatments, with general physical condition or related adverse reactions having recovered (toxicity ≤ grade 1) or stabilized;\n* Willing to participate and sign the informed consent form;\n* Good compliance and agreement to cooperate with survival follow-up.\n\nExclusion Criteria:\n\n* Subjects with ascites requiring clinical intervention (including moderate to large amounts of ascites; subjects with ascites need to be stable for more than 4 weeks after drainage);\n* Clinically severe gastrointestinal diseases (including bleeding, infectious inflammation, perforation, obstruction, or diarrhea greater than grade 1);\n* NRS pain score ≥ 4 after standardized treatment with analgesics;\n* Second primary malignancy within 5 years (except cured carcinoma in situ, basal cell, or squamous cell skin cancer; subjects with other previous tumors can be enrolled if there has been no recurrence within 5 years);\n* Uncontrolled cardiovascular or cerebrovascular diseases with clinical symptoms, including but not limited to: ① NYHA class III or higher heart failure; ② unstable angina; ③ myocardial infarction or stroke within 6 months; ④ supraventricular or ventricular arrhythmias requiring treatment or intervention; ⑤ uncontrolled hypertension (systolic blood pressure \\&gt; 150 mmHg and\u002For diastolic blood pressure \\&gt; 90 mmHg despite optimal treatment);\n* Known active hepatitis B subjects (HBsAg positive and HBV DNA ≥ 10³ copies or ≥ 1000 U\u002Fml);\n* Active infection or unexplained fever \\&gt; 38.5°C during the screening period or on the day of administration (subjects with fever caused by tumors can be enrolled as judged by the investigator), which, in the investigator\\&#39;s judgment, would affect the subject\\&#39;s participation in this trial or interfere with the evaluation of efficacy;\n* Pregnant or breastfeeding women;\n* Women of childbearing potential with a positive blood (urine) pregnancy test during the screening period (both male and female subjects should use reliable contraception during the trial and for 3 months after the last dose to prevent pregnancy);\n* Subjects with other medical or social issues that, in the investigator\\&#39;s judgment, might affect their ability to sign informed consent, participation in the trial, or interpretation of the trial results;\n* Patients with an estimated survival time of ≤ 3 months are not included in this study.","ALL","18 Years",{"count":19,"type":20},50,"ESTIMATED","INTERVENTIONAL",[23],"PHASE2","This Phase II clinical study evaluates the safety and efficacy of a combination therapy for patients with pancreatic cancer that has spread to the liver. Because liver metastases are a major factor in the progression of pancreatic cancer, this research utilizes Hepatic Arterial Infusion Chemotherapy (HAIC) to deliver high-concentration treatment directly into the tumor's blood supply. The multi-step strategy involves first infusing Sodium Bicarbonate to neutralize the acidic tumor microenvironment , followed by the NASOX chemotherapy regimen (Oxaliplatin and Liposomal Irinotecan) and an intra-arterial PD-1 inhibitor to boost immune response. Patients also receive oral S-1 to maintain treatment effect. The primary goal is to determine if this integrated approach can improve Overall Survival for patients compared to historical standard treatments.",[26,27],"Pancreatic Neoplasms","Hepatic Metastasis of Pancreatic Cancer","RECRUITING","2026-03-26",{"date":31,"type":32},"2026-03-31","ACTUAL",{"date":34,"type":20},"2026-03-23",{"date":36,"type":20},"2027-12-31",{"name":38,"class":39},"Ruijin Hospital","OTHER"]