[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"high-risk-large-b-cell-lymphoma-lbcl\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:high-risk-large-b-cell-lymphoma-lbcl":43},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":27,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":5},"100587957",false,"NCT06935136","Study to Evaluate the Efficacy and Safety of Axicabtagene Ciloleucel Injection as First-Line Therapy of High-Risk Large B-Cell Lymphoma","A Single-Arm, Multicenter, Open-Label Clinical Study to Evaluate the Efficacy and Safety of Axicabtagene Ciloleucel Injection as First-Line Therapy of High-Risk Large B-Cell Lymphoma","Inclusion Criteria:\n\n* Histologically confirmed LBCL (Large B-Cell Lymphoma) according to the WHO 2016 classification, including the following subtypes:DLBCL-NOS (Diffuse Large B-Cell Lymphoma, Not Otherwise Specified),HGBL (High-Grade B-Cell Lymphoma, including HGBL with MYC, BCL-2, and\u002For BCL-6 rearrangements (DHL\u002FTHL), HGBL-NOS),DLBCL transformed from follicular or marginal zone lymphoma, eligible if the patient has not previously received anthracycline-containing therapy\n* International Prognostic Index (IPI) score of 2-5 at initial diagnosis.\n* Individuals must have a positive interim positron emission tomography (PET) (Deauville PET score of 4 or 5) after 2 cycles (PET2+) of chemoimmunotherapy or high-risk ctDNA status (ctDNA levels not reduced by at least 2-log after two cycles of R-chemotherapy)\n* Age of 18 years or older.\n* Eastern Cooperative Oncology Group (ECOG) performance status score of 0-2.\n* Adequate renal, hepatic, pulmonary, and cardiac function, defined as:\n\n  * Creatinine clearance (estimated by Cockcroft-Gault formula) ≥ 60 mL\u002Fmin\n  * Serum ALT\u002FAST ≤ 2.5 × Upper Limit of Normal (ULN)\n  * Total bilirubin ≤ 1.5 × ULN (except for patients with Gilbert's syndrome)\n  * Left ventricular ejection fraction ≥ 50%, no pericardial effusion as determined by echocardiography, and no clinically significant arrhythmias No clinically significant pleural effusion\n  * Baseline peripheral oxygen saturation \\> 92% under room air ventilation\n  * At least one measurable lesion.\n  * For women of childbearing potential, a negative serum pregnancy test is required (women who have undergone surgical sterilization or are postmenopausal for at least 2 years are considered not to be of childbearing potential).\n\nExclusion Criteria:\n\n* According to the WHO 2016 classification, patients with the following subtypes are excluded:\n\n  * LBCL with T-cell\u002Fhistiocyte-rich background\n  * Primary central nervous system DLBCL\n  * PMBCL (Primary Mediastinal B-Cell Lymphoma)\n  * B-cell lymphoma, unclassifiable, with features intermediate between DLBCL and classical HL (Hodgkin Lymphoma)\n  * Burkitt lymphoma\n  * History of Richter transformation in chronic lymphocytic leukemia\n* Presence of detectable malignant cells in the CSF (cerebrospinal fluid), brain metastases, or history of central nervous system involvement by lymphoma.\n\nPresence of cardiac involvement by lymphoma.\n\n* Prior treatment for LBCL other than two cycles of R-chemotherapy.\n* History of severe immediate hypersensitivity reaction to any of the drugs used in this study.\n* Presence of central nervous system disorders: history of stroke, transient ischemic attack, or reversible posterior leukoencephalopathy syndrome (PRES) within 12 months prior to enrollment.\n* History of acute or chronic active hepatitis B or C infection, unless HBV-DNA and HCV-RNA levels are below the level of detection.\n* Human immunodeficiency virus (HIV) positivity, unless on appropriate antiretroviral therapy with undetectable viral load by PCR and a CD4 count \\> 200 cells\u002FµL.\n* Any medical condition that may interfere with the assessment of the safety or efficacy of the study treatment.\n* History of clinically significant cardiac disease within 12 months prior to enrollment.\n* Any other condition deemed by the investigator as unsuitable for enrollment.","ALL","18 Years",{"count":18,"type":19},60,"ESTIMATED","INTERVENTIONAL",[22],"NA","The goal of this is Single-Arm, Multicenter, Open-Label Clinical Study is to Evaluate the Efficacy and Safety of Axicabtagene Ciloleucel Injection(Axi-cel) as First-Line Therapy of High-Risk Large B-Cell Lymphoma.",[25,26],"CAR-T Cell Therapy","High-risk Large B-cell Lymphoma (LBCL)",[28,29,30],"axi-cel","car-t","LBCL","NOT_YET_RECRUITING","2025-04-21",{"date":34,"type":35},"2025-04-22","ACTUAL",{"date":37,"type":19},"2025-04-30",{"date":39,"type":19},"2028-04-09",{"name":41,"class":42},"Ruijin Hospital","OTHER",""]