RecruitingPhase 1Phase 2NCT06530303

Biological Tumor Infiltrating Lymphocytes Therapy With Immunotherapy for Colon and Rectum Cancer

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


Sponsor

Essen Biotech

Enrollment

85 participants

Start Date

Sep 29, 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) and Aldesleukin (interleukin-2, IL-2) immunotherapy in patients with advanced or metastatic refractory colon and rectal cancer (colorectum). 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, while Aldesleukin will be used to further stimulate the TILs. 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 provide 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 is testing a treatment for colon and rectal cancer that uses the patient's own tumor-fighting immune cells (called tumor-infiltrating lymphocytes, or TILs), grown and expanded in a lab, combined with immunotherapy drugs. This is called biological TIL therapy. **You may be eligible if...** - You are between 16 and 90 years old - You have a histologically confirmed colorectal cancer (primary, relapsed, or metastatic) - Your cancer has failed standard treatments, or no standard treatment is available - You have a tumor that can be biopsied or removed to harvest TILs - Your general health is acceptable (able to perform basic daily activities) - Your estimated survival is more than 3 months **You may NOT be eligible if...** - Your cancer has no accessible tumor tissue for TIL extraction - Your health is too poor to tolerate the treatment - You have autoimmune conditions that would react badly to immunotherapy 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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NCT06530303


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