About this trial
Hepatocellular carcinoma (HCC) is the most common liver primary cancer with a high rate of mortality. Since the results of IMbrave150, immunotherapy have emerged as a standard of care for HCC patients advanced and/or unresectable in first line of treatment. The objective response rate was about 30%, but half of patients would present only stable disease and about 20% progressive disease.
Faecalibacterium prausnitzii is one of the most abundant bacterial in human gut microbiota, around 5% of total bacteria in feces.
For patients with metastatic melanoma, treated with ipilimumab, an antibody targeting CTLA-4 (Cytotoxic T-lymphocyte-associated antigen 4), patients with a baseline gut microbiota enriched with Faecalibacterium had a significantly better clinical outcomes. In patients with metastatic melanoma, the level of Faecalibacterium prausnitzi at baseline was predictive of response to anti-PD-1 (programmed death-1) or anti-CTLA-4 therapy. EXL01 is a pharmacological preparation of Faecalibacterium prausnitzii strains. Preclinical murine study suggests that the administration of EXL01 could reverse the resistance to ICI induced by antibiotics (unpublished data).
We thus plan to test the concept of microbiota modification in patients treated with standard-of-care approved first-line immunotherapy for advanced HCC. We would include patients refractory to first-line treatment, and test the addition of EXL01 to standard-of-care approved first-line immunotherapy in order to reverse resistance.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Male and Female
Age ≥18 years at time of signing informed consent
Presenting with HCC, diagnosed either by histological or radiological criteria as described by EASL
Locally advanced or metastatic and/or unresectable HCC according a Multidisciplinary Team meeting
Disqualifiers
Partial response achieved under standard-of-care approved first-line immunotherapy
CTCAE Grade ≥3 or more toxicity under standard-of-care approved first-line immunotherapy, or persistent toxicity Grade >1
Liver involvement > 50%
Presence of major macro vascular invasion (except Vp1/Vp2)
Trial design
Single group
Treatments tested in this trial
EXL01
DrugEXL01 contains an unmodified single strain of F. prausnitzii
Treatment groups
Trial outcomes
Primary outcomes
Objective Response Rate at week12
ORR defined as the best observed overall tumor response (BOR) from inclusion to W12, according RECIST 1.1 criteria
Adverse event
safety of atezolizumab-bevacizumab with bacterial supplementation EXL01
Secondary outcomes
Overall tumor response
Overall tumor response according to the mRECIST, RECIST 1.1 and iRECIST.
Objective Response Rate at week12
ORR at week 12 according to mRECIST and iRECIST criteria
Objective Response Rate at M6 and M12
The ORR at M6, M12, according to the mRECIST, RECIST 1.1 and iRECIST criteria.
The Disease control rate (DCR),
The Disease control rate (DCR), as the proportion of patients with BOR as CR, PR or stable disease (SD) defined according to the mRECIST, RECIST 1.1 and iRECIST criteria at W12, M6, M12.
Sponsors and contacts
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