Fast TILs for Metastatic Cancer with Pleural Disease
This study is testing a new immunotherapy called Fast TILs to treat cancers that have spread to the lining of the lungs (pleura) or malignant mesothelioma. This treatment uses your own immune cells, specifically T-cells from your pleural fluid, which are grown in a lab at AHN West Penn. These special cells are then put back into your chest through a catheter, along with a drug called Interleukin-2 (IL-2). The main goal is to see if this treatment can be made locally and if it's safe. You might be able to join if you are between 18 and 79 years old, have cancer that has spread to your pleura or mesothelioma with fluid buildup, and standard treatments haven't worked. The study plans to enroll 10 participants, but its current status is unclear.
- Study design
- This is a first-in-human, single-arm study (meaning all participants receive the same treatment) that plans to enroll 10 participants.
- What's involved
- You will have pleural fluid collected, undergo chemotherapy, and then receive the Fast TILs and Interleukin-2 through a pleural catheter.
- Compensation
- Not stated in the trial record.
- Follow-up
- The feasibility of manufacturing the treatment is measured at 30 days after treatment.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Fast TILs to Treat Metastatic Cancer Patients With Pleural Disease
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- David Bartlett, MD · PRINCIPAL_INVESTIGATOR · Allegheny Health Network
Who to contact
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What this trial measures
- Document the feasibility of local manufacture of ACT product from drained pleural effusions using the CliniMACS Prodigy® device30 days
flow cytometry for cellular ACT identity
- Document the feasibility of local manufacture of ACT product from drained pleural effusions using the CliniMACS Prodigy® device30 days
cytotoxicity assays for ACT potency
- Document the feasibility of local manufacture of ACT product from drained pleural effusions using the CliniMACS Prodigy® device30 days
flow cytometry for cellular ACT purity
- To demonstrate the safety of intrapleural administration of the locally manufactured ACT product plus Interleukin 2 (IL-2) to study patients5 years
incidence of Treatment-Emergent Adverse Events (Safety) of intrapleural administration of the locally manufactured ACT product, as assessed by Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.