Identification of an Immune Single Cell Transcriptomic Profile of Responder and Non-responder Hepatocellular Carcinoma Patients Treated With Immune-checkpoint Inhibitors

Recruiting now

Conditions studied: Advanced HCC Treated by Systemic Immunotherapy

In brief

The study aims to analyze blood samples from patients with advanced hepatocellular carcinoma who are receiving systemic treatment with immunotherapy. The objective is to determine whether treatment exposure leads to changes in the transcriptomic patterns of peripheral blood mononuclear cells (PBMCs), if these changes are associated with treatment response, and whether certain pre-treatment transcriptomic signatures can predict response to treatment. As an exploratory objective, PBMCs derived from patients exposed to immune checkpoint inhibitors will be co-cultured with their paired tumor cells in organoid cultures. This aims to assess whether these preclinical 3D models correlate with clinical outcomes.

Key facts

Study ID

NCT07273708

Run by

Fondazione IRCCS Policlinico San Matteo di Pavia

People needed

20

Starts

2025-03-15

Expected to finish

2026-07-01

Last updated by the study team

2025-12-09

Who can join

Age: 18 and older, up to 90. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• diagnosis of advanced HCC treated with atezolizumab plus bevacizumab or tremelimumab single dose plus durvalumab (STRIDE regimen) as first-line treament
• age ≥18 and <90 years at time of signing informed consent
• Signed Informed Consent Form

You may not qualify if…

• Life expectancy of <12 months due to concomitant diseases
• Active or history of autoimmune disease or immune deficiency on inflammatory chronic diseases
• Ongoing drug abuse
• History of malignancy other than HCC within 3 years prior to study entry with the following exception:
• Completely resected malignancies with a negligible risk of metastasis or death (e.g., 5-year OS rate 90%) and without evidence of recurrence for > 3 years prior to study entry
• adequately treated non-melanoma skin carcinoma or lentigo maligna without evidence of metastases.
• adequately treated carcinoma in situ of the cervix without evidence of recurrence
• localised prostate cancer
• adequately treated non invasive or in situ urothelial cancers
• evidence or history of positive HIV test
• inability to comply with the study protocol, in the investigator's judgment

Where it is running

• Fondazione IRCCS Policlinico San Matteo — Pavia, Lombardy, Italy (enrolling)

Full record on ClinicalTrials.gov

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