Microbiota Modification for Immuno-oncology in Hepatocellular Carcinoma

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorCenter Eugene Marquis

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murine study suggests that the administration of EXL01 could reverse the resistance to ICI induced by antibiotics (unpublished data).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 volunteers

Qualifiers

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

Design model

Single group

Treatments tested in this trial

  • EXL01

    Drug

    EXL01 contains an unmodified single strain of F. prausnitzii

Treatment groups

34 Participants
are divided into 1 treatment group
Group A: standard-of-care approved first-line immunotherapy- EXL01Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Objective Response Rate at week12

ORR defined as the best observed overall tumor response (BOR) from inclusion to W12, according RECIST 1.1 criteria

Time frame
At week12
2

Adverse event

safety of atezolizumab-bevacizumab with bacterial supplementation EXL01

Time frame
Maximum 15 month after le first EXL01 administration

Secondary outcomes

1

Overall tumor response

Overall tumor response according to the mRECIST, RECIST 1.1 and iRECIST.

Time frame
At week6; at week12; at month 6, at month12
2

Objective Response Rate at week12

ORR at week 12 according to mRECIST and iRECIST criteria

Time frame
at week 12
3

Objective Response Rate at M6 and M12

The ORR at M6, M12, according to the mRECIST, RECIST 1.1 and iRECIST criteria.

Time frame
At month 6, at month 12
4

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.

Time frame
At week12; at month 6, at month12

Other outcomes

Sponsors and contacts

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