Study on TIL Engineered With Membrane-Binding Cytokine for the Treatment of Advanced Gynecologic Tumors

Launched by SHANGHAI JUNCELL THERAPEUTICS · Jul 20, 2022

Keywords

ClinConnect Summary

This clinical trial is exploring a new treatment option for women with advanced gynecologic tumors that have not responded to standard therapies. The study is testing a special type of immune cell therapy called TIL (tumor-infiltrating lymphocytes) that has been modified to enhance its effectiveness. These modified cells are taken from the patient's own tumor tissue, grown in the lab, and then infused back into the patient after a short treatment to prepare their body. The main goals are to assess how safe this treatment is and whether it can help improve the patients' condition.

To participate in this trial, women aged 18 to 75 who have been diagnosed with advanced gynecologic tumors may be eligible if they have already tried other treatments without success. Candidates should have enough healthy cells in their blood and a tumor that can be sampled. Participants can expect close monitoring throughout the study, as researchers will track any side effects and the treatment's effectiveness. It's important to note that those with certain health conditions, such as severe heart or lung issues, or ongoing infections, may not qualify for this trial.

Gender

FEMALE

Eligibility criteria

• Inclusion Criteria:
• • 1. Age: 18 years to 75 years;
• • 2. Histologically diagnosed as primary/relapsed/metastasized Gynecological tumors;
• • 3. Expected life-span more than 3 months;
• • 4. Karnofsky≥60% or ECOG score 0-2;
• • 5. Test subjects have failed standard treatment regimens, or there are no standard treatment regimens available.
• • 6. Test subjects must have tumor regions eligible for biopsy or resection, or malignant body fluid where TILs can be isolated;
• • 7. At least 1 evaluable tumor lesion;
• 8. Hematology and Chemistry（within 7 days prior to enrollment）:
• • Absolute count of white blood cells≥2.5×10\^9/L;
• • Absolute count of neutropils≥1.5×10\^9/L;
• • Absolute count of lymphocytes ≥0.7×109/L；
• • Platelet count≥100×10\^9；
• • hemoglobin≥90 g/L;
• • Activated partial thromboplastin time (APTT) ≤1.5xULN (Unless received anticoagulant therapy within the previous 3 days);
• • International normalized ratio (INR) ≤1.5xULN (Unless received anticoagulant therapy within the previous 3 days);
• • Serum creatinine ≤1.5mg/dL(or ≤132.6μmol/L), or clearance rate≥50mL/min;
• • Serum ALT/AST ≤3×ULN(subjects with liver metastasis ≤3×ULN);
• • Totol bilirubin≤1.5×ULN;
• • 9. no absolute or relative contraindications to operation or biopsy;
• • 10. Test subjects with child-bearing potential must be willing to practice approved highly effective methods of contraception at the time of informed consent, and continue within 1 year after the completion of lymphodepletion；
• • 11. Any malignant tumor-targeting therapies, including radiotherapy, chemotherapy and biologics must cease 28 days before obtaining TILs;
• • 12. Be able to understand and sign the informed consent document;
• • 13. Be able to stick to follow-up visit plan and other requirements in the agreement.
• Exclusion Criteria:
• • 1. Need glucocorticoid treatment, and daily dose of Prednisone greater than 15mg (or equivalent doses of hormones) or outoimmune diseases requiring immunomodulatory treatment;
• • 2. Forced expiratory volume in one second (FEV1) less than 2L, diffusing capacity of the lung for carbon monoxide (DLCO) (calibrated) less than 40%;
• • 3. Significant cardiovascular anomalies according to any of the following definition: New York Heart Association (NYHA) Grade III or IV congestive heart failure, clinically significant low blood pressure, uncontrollable symptomatic coronary artery diseases, or ejection fraction less than 35%; Severe cardiac rhythm and conduction anomaly, such as ventricular arrhythmia requiring clinical intervention, second-third degree atrio-ventricular conductive block, etc.
• • 4. Human immunodeficiency virus (HIV) infection or anti-HIV antibody positive, active HBV or HCV infection (HBsAg positive and/or anti-HCV positive), syphilis infection or Treponema pallidum antibody positive;
• • 5. Severe physical or mental diseases;
• • 6. Have a systemic active infection requiring treatment, or have positive blood cultures(or imaging evidence of infection);
• • 7. Having been treated within a month or being treated now with other medicines, or other biologic therapy, chemo-or radiotherapy;
• • 8. History of allergy to chemical compound consisting of chemical and biologic substances resembling cell therapy;
• • 9. Having received immunotherapy and developed irAE level greater than Level 3;
• • 10. Previous anti-tumor treatment AE did not return to CTCAE5.0 version grade 1 or below (toxicity considered by the investigator as non-safety concerns like alopecia excluded);
• • 11. Females in pregnancy or lactation;
• • 12. History of organ transplantation, allogeneic stem cell transplantation, and renal replacement therapy;
• • 13. Researchers considering the test subject as having a history of other severe systemic diseases, or other reasons inappropriate for the clinical study.