[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"anti-pd1pdl1-antibody\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:anti-pd1pdl1-antibody":26},{"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":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":28,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":5},"100540940","locoregional-therapy-combined-with-bevacizumab-and-pd1l1-inhibitor-in-advanced-hepatocellular-carcinoma-100540940",false,"NCT06323382","Locoregional Therapy Combined With Bevacizumab and PD1\u002FL1 Inhibitor in Advanced Hepatocellular Carcinoma","Efficacy of Locoregional Therapy Combined With Bevacizumab and PD1\u002FL1 Inhibitor in Advanced Hepatocellular Carcinoma: a Multicenter, Observational, Real-world Study","Inclusion Criteria:\n\n1. HCC diagnosed by histopathological examination or Guidelines for Diagnosis and Treatment of Primary Liver Cancer or the recurrent HCC after surgery;\n2. age between 18 and 75 years;\n3. Stage B (middle stage) or C (late stage) HCC determined in accordance with Barcelona Clinic Liver Cancer staging system (BCLC stage).\n4. Locoregional therapy include TACE or HAIC, locoregional combined with Bevacizumab and PD1\u002FL1 inhibitor as firstline therapy; non-firstline therapy (previous use of any systemic therapy but intolerant or drug resistant).\n5. Child-Pugh class A or B;\n6. Eastern Cooperative Group performance status (ECOG) score of 0-2;\n7. Hemoglobin ≥ 8.5 g\u002FdL Total bilirubin ≤ 30mmol\u002FL Serum albumin ≥ 32 g\u002FL ASL and AST ≤ 5 x upper limit of normal Serum creatinine ≤ 1.5 x upper limit of normal INR ≤ 1.5 or PT\u002FAPTT within normal limits Absolute neutrophil count (ANC) \\>1,500\u002Fmm3\n8. Prothrombin time ≤18s or international normalized ratio \\\u003C 1.7.\n9. Ability to understand the protocol and to agree to and sign a written informed consent document.\n\nExclusion Criteria:\n\n1. Cholangiocellular carcinoma (ICC).\n2. Patients without image information should be excluded;\n3. The survival or patients less than 3 months.\n4. Serious medical comorbidities.\n5. Evidence of hepatic decompensation including ascites, gastrointestinal bleeding or hepatic encephalopathy.\n6. Known history of HIV.\n7. History of organ allograft.\n8. Known or suspected allergy to the investigational agents or any agent given in association with this trial.\n9. Cardiac ventricular arrhythmias requiring anti-arrhythmic therapy.\n10. Evidence of bleeding diathesis.\n11. Patients with clinically significant gastrointestinal bleeding within 30 days prior to study entry.","ALL","18 Years","80 Years",{"count":20,"type":21},240,"ESTIMATED","OBSERVATIONAL","Atezolizumab + Bevacizumab was superior to sorafenib in overall survival in advanced hepatocellular carcinoma. The programmed cell death protein-1 (PD1) and PDL1 inhibitor, was effective and tolerable in patients with advanced hepatocellular carcinoma. We aimed to describe the efficacy and safety of locoregional therapy combined with Bevacizumab and PD1\u002FL1 inhibitor in patients with advanced hepatocellular carcinoma who can not receive radical therapy.",[25,26,27],"Advanced Hepatocellular Carcinoma","Anti-PD1\u002FPDL1 Antibody","Bevacizumab",[27,29,30,31,32,33],"Atezolizumab","Tislelizumab","Toripalimab","Sintilimab","Camrelizumab","RECRUITING","2025-08-10",{"date":37,"type":38},"2025-08-14","ACTUAL",{"date":40,"type":38},"2021-01-01",{"date":42,"type":21},"2025-12-30",{"name":44,"class":45},"Sun Yat-sen University","OTHER"]