TALENT Study: Phase II Trial of Adjuvant L-TIL Plus Tislelizumab in Resectable NSCLC Without pCR After Neoadjuvant Chemoimmunotherapy

Official title

A Prospective Phase II Clinical Trial Evaluating Liquid Tumor-infiltrating Lymphocytes (L-TIL) in Combination With Tislelizumab as Adjuvant Therapy in Patients With Resectable Stage II to IIIB (N2) Non-small Cell Lung Cancer (NSCLC) Who Have Undergone Surgery Following Neoadjuvant Treatment With an Immune Checkpoint Inhibitor Plus Platinum-based Doublet Chemotherapy and Did Not Achieve a Pathological Complete Response (pCR)

Overview

This study evaluates the preliminary efficacy and safety of adjuvant therapy with liquid tumor-infiltrating lymphocytes (L-TIL) in combination with tislelizumab in patients with resectable stage II-IIIB non-small cell lung cancer (NSCLC) who underwent surgery after neoadjuvant treatment with an immune checkpoint inhibitor plus platinum-based doublet chemotherapy but did not achieve a pathological complete response (pCR).

Interventions

• Biological L-TIL cells injection
  Autologous peripheral blood TILs will be infused 4 times, each at a dose of ≥1 × 10⁹ cells, administered 2-3 days after each tislelizumab infusion.
• Drug Tislelizumab
  Tislelizumab will be given at 400 mg every 6 weeks for a total of 8 cycles of adjuvant treatment.

Primary outcome measures

• 2-year Disease Free Survival [Time frame: 2 years]

Secondary outcome measures (6)

• Disease free survival (DFS) [Time frame: Up to 3 years]
• Overall survival (OS) [Time frame: Up to 5 years]
• Adverse event (AE) [Time frame: Up to 5 years]
• Locoregional Recurrence-Free Survival (LRFS) [Time frame: Up to 3 years]
• Distant Metastasis-Free Survival (DMFS) [Time frame: Up to 3 years]
• Lung Cancer-Specific Survival (LCSS) [Time frame: Up to 5 years]

Eligibility criteria

Inclusion criteria

• Histologically or cytologically confirmed NSCLC with imaging indicating resectable stage II-IIIB (N2) disease according to the ninth edition of the AJCC lung cancer TNM staging system;
• No prior anti-tumor treatment;
• Negative for EGFR/ALK/ROS1 mutations;
• Eastern Cooperative Oncology Group (ECOG) performance status score of 0-1;
• Undergone 2-4 cycles of neoadjuvant therapy combining immunotherapy and chemotherapy, followed by surgical resection with R0 margins but without achieving a complete pathological response (non-pCR);
• Adequate organ function as defined below (without using any blood products or hematopoietic growth factors within 14 days):

Normal bone marrow reserve: neutrophil count ≥1.5×10⁹/L, lymphocyte count ≥0.6×10⁹/L, platelet count ≥100×10⁹/L, hemoglobin ≥90g/L; Normal renal function: serum creatinine ≤1.5 mg/dL and/or creatinine clearance rate ≥60 mL/min; Normal liver function: total bilirubin ≤1.5 times ULN, AST and ALT ≤1.5 times ULN; Normal coagulation function: APTT ≤1.5 times ULN, INR ≤1.5 times ULN, PT ≤1.5 times ULN; Left ventricular ejection fraction (LVEF) ≥50% on echocardiography; Pulmonary function test showing FEV1 ≥60%;

• For non-surgically sterilized or women of childbearing potential, must agree to use medically approved contraception (such as an intrauterine device, contraceptive pills, or condoms) during the study treatment period and for 3 months after the end of treatment; must have a negative serum or urine HCG test within 7 days prior to study entry; must not be breastfeeding;

Exclusion criteria

• Vaccination within 28 days prior to the first dose, except for inactivated vaccines;
• Major surgery within 28 days prior to the first dose;
• History of other malignancies within 5 years prior to screening;
• Congenital or acquired immunodeficiency, such as HIV infection, or active hepatitis (for inclusion criteria, ALT and AST levels must be within specified limits; for hepatitis B: HBV DNA >10\^4/ml; for hepatitis C: HCV RNA >10\^3/ml; for chronic hepatitis B carriers, HBV DNA >2000 IU/ml (>10\^4 copies/ml), antiviral treatment must be concurrently administered during the study period);
• Unstable or severe concurrent diseases within 6 months prior to the first dose, such as severe/unstable angina pectoris, symptomatic congestive heart failure, myocardial infarction, pulmonary hypertension, life-threatening ventricular arrhythmias requiring maintenance therapy, stroke, and uncontrolled severe seizures;
• Clinically significant active pneumonia or other respiratory system diseases severely affecting lung function at screening;
• Active autoimmune diseases, history of autoimmune diseases, or conditions requiring systemic corticosteroids or immunosuppressive drugs;
• Arterial or venous thrombotic events occurring within 6 months prior to screening;
• History or CT findings indicating active tuberculosis within 1 year prior to enrollment that was untreated;
• Active infections requiring systemic anti-infective treatment;
• Active gastrointestinal bleeding or contraindications to IL-2 use;
• Previous bone marrow transplant or solid organ transplant;
• Other serious acute or chronic medical or psychiatric illnesses (including suicidal ideation or behavior within one year) that may increase the risk associated with participation in the study or administration of the investigational treatment, interfere with the investigational treatment and follow-up, or affect the subject's compliance;

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

N/A

Model

Single group

Masking

Open label

Primary purpose

Treatment

Study locations

China · 1 center

• Tianjin Medical University Cancer Institute and Hospital — Tianjin

Identifiers

NCT: NCT07330037 · TALENT

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗