Efficacy and Safety of MSLN CAR-T in Advanced Malignant Tumors

Detailed Description:

This is a prospective, interventional Phase I/II clinical study designed to evaluate the safety and efficacy of MSLN-targeted CAR-T cell therapy in patients with advanced malignant tumors. A total of 20 patients aged 18-75 years with unresectable, locally advanced, recurrent, or metastatic solid malignancies will be enrolled. All patients must have histopathologically confirmed disease and positive MSLN expression in tumor tissue.

MSLN CAR-T cells will be administered as a single intravenous infusion at a total dose of 0.5-2 × 10^6 CAR-T cells/kg. Eligible subjects (N=20) will be assigned by the investigator to receive MSLN CAR-T cell infusion.

Endpoints:

• Primary Endpoint:

o Incidence and severity of treatment-emergent adverse events (TEAEs) within 30 days after MSLN CAR-T cell infusion.

• Secondary Endpoints:

• Objective response rate (ORR = CR + PR) assessed within 8 weeks after infusion;
• Overall survival (OS) and progression-free survival (PFS) at 6 months;
• In vivo expansion and persistence kinetics of infused CAR-T cells.

Inclusion criteria

• Aged 18-75 years (≥18 and ≤75 years), either sex;
• The subject voluntarily participates in the study and provides written informed consent signed by the subject or his/her legally authorized representative;
• Histopathologically confirmed unresectable, locally advanced, recurrent, or metastatic solid malignant tumor; according to the AJCC TNM staging system (8th edition, 2017), subjects diagnosed with stage III or stage IV solid malignant tumors;
• Presence of measurable and evaluable lesions according to RECIST v1.1;
• Positive MSLN expression in tumor tissue confirmed by immunohistochemistry (IHC);
• The subject must have received standard first-line therapy and has experienced disease progression or is intolerant to such therapy;
• The subject is not suitable for curative treatment modalities such as definitive chemoradiotherapy and/or surgery/immune checkpoint inhibitors, or refuses surgical resection;
• No antibody-based therapy administered within 2 weeks prior to cell therapy;
• ECOG performance status 0-2;
• No contraindications to peripheral blood leukapheresis;
• Estimated life expectancy ≥ 3 months.

Exclusion criteria

• History of allergy to any component of the cell product;
• Any of the following hematologic abnormalities on complete blood count (CBC): WBC ≤ 1 × 10^9/L, absolute neutrophil count (ANC) ≤ 0.5 × 10^9/L, absolute lymphocyte count (ALC) ≤ 0.5 × 10^9/L, or platelets (PLT) ≤ 25 × 10^9/L;
• Any of the following laboratory abnormalities, including but not limited to: serum total bilirubin ≥ 1.5 mg/dL; serum ALT or AST > 2.5 × ULN; serum creatinine ≥ 2.0 mg/dL;
• NYHA class III or IV heart failure per the New York Heart Association functional classification, or left ventricular ejection fraction (LVEF) < 50% on echocardiography;
• Abnormal pulmonary function with oxygen saturation (SpO₂) < 92% on room air;
• History of myocardial infarction, coronary angioplasty or stenting, unstable angina, or other clinically significant severe cardiac disease within 12 months prior to enrollment;
• Grade 3 hypertension with poor blood pressure control despite medical treatment;
• History of traumatic brain injury, disturbance of consciousness, epilepsy, or severe cerebral ischemic or hemorrhagic disease;
• Presence of autoimmune disease, immunodeficiency, or other conditions requiring immunosuppressive therapy;
• Presence of uncontrolled active infection;
• Prior treatment with any CAR-T cell product or other genetically modified T-cell therapy;
• Receipt of a live vaccine within 4 weeks prior to enrollment;
• Positive test results for HIV, HBV, HCV, and TPPA/RPR, and/or HBV carriers;
• History of alcohol abuse, illicit drug use, or psychiatric disorders;
• Participation in any other clinical study within 3 months prior to enrollment;
• Female subjects meeting any of the following:

• pregnant or breastfeeding; or
• planning pregnancy during the study period; or
• of childbearing potential and unable/unwilling to use effective contraception;
• Any other condition that, in the opinion of the investigator, makes the subject unsuitable for participation in this study.