RecruitingPhase 1Phase 2NCT06538012

TIL Therapy Combined With Pembrolizumab for Advanced or Metastatic Refractory Lung Cancer

Efficacy and Safety of Autologous Tumor-Infiltrating Lymphocytes (TIL) Therapy Combined With Pembrolizumab Immunotherapy in Patients With Advanced or Metastatic Refractory Lung Cancer


Sponsor

Essen Biotech

Enrollment

85 participants

Start Date

Aug 20, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This Phase I/II study evaluates the safety and efficacy of autologous tumor-infiltrating lymphocytes (TIL) therapy combined with Pembrolizumab (Keytruda) immunotherapy in patients with advanced or metastatic refractory lung cancer. Lifileucel (Amtagvi), the first FDA-approved TIL therapy, has demonstrated significant success in treating unresectable or metastatic melanoma by utilizing the patient's own immune cells to combat cancer. This study aims to apply a similar approach to lung cancer. TILs will be harvested from patients' tumors, expanded in vitro, and infused back into the patients following a non-myeloablative lymphodepletion regimen. Pembrolizumab, a monoclonal antibody targeting the PD-1 receptor on T cells, will be administered to enhance the immune response. The primary endpoint is to determine the objective response rate (ORR) of this combined therapy. Secondary endpoints include disease control rate (DCR), progression-free survival (PFS), overall survival (OS), duration of response (DOR), and quality of life (QoL). This trial aims to offer a novel, personalized treatment option for patients with limited therapeutic alternatives.


Eligibility

Min Age: 16 YearsMax Age: 90 Years

Plain Language Summary

Simplified for easier understanding

This study tests a combination of TIL therapy (using a patient's own immune cells grown from their tumor) plus pembrolizumab (an immunotherapy drug) for advanced or metastatic lung cancer that has not responded to standard treatments. **You may be eligible if...** - You are aged 16–90 with confirmed primary, relapsed, or metastatic lung cancer - Your cancer has failed standard treatment options - Your tumor can be biopsied or surgically accessed to collect immune cells - You have at least one measurable tumor and are in reasonable physical condition (ECOG 0–2) **You may NOT be eligible if...** - You have very low blood counts or poor organ function - You have active autoimmune disease or serious uncontrolled infection - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BIOLOGICALTumor Infiltrating Lymphocytes (TIL)

Tumor Infiltrating Lymphocytes (TIL) IV

DRUGCyclophosphamide

Cyclophosphamide will be administered as an intravenous (IV) infusion for two days.

DRUGFludarabine

Fludarabine will be administered as an intravenous (IV) infusion for five days.

DRUGInterleukin-2

After TIL infusion, IL-2 will be started as a bolus administration every eight hours, for a maximum of eight doses.

DRUGPembrolizumab

Intravenous (IV) infusion


Locations(1)

District One Hospital

Beijing, Beijing Municipality, China

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NCT06538012


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