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RecruitingNCT05878977Updated Oct 18, 2024

Biomarkers in Immunotherapy of Melanoma

An interventional study of Immune checkpoint inhibitor in Metastatic Melanoma, Immune Checkpoints Inhibitors and Gastrointestinal Microbiome (Bacterial and Viral), sponsored by Institute of Oncology Ljubljana. Recruiting at 1 site in Slovenia. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-10-18.

Sponsored by Institute of Oncology Ljubljana · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Oct 2022, registered Apr 2023).
  • Started Oct 2022; still recruiting 4 years later.
Phase
Not applicable
Study type
Interventional
Enrollment
150
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

Background: Immunotherapy has been successful in treating advanced melanoma, but a large proportion of patients do not respond to the treatment with immune checkpoint inhibitors (ICIs). Preclinical and small cohort studies suggest biomarkers from the primary tumor, stool and body fluids as markers of response. This prospective study will evaluate gastrointestinal microbiome (bacterial spices and virome) composition and exosomal mRNA expression of PD-L1 and IFNγ correlation with radiological response rates to ICIs treatment of advanced melanoma patients. Methods: Patients treated with immune checkpoint inhibitors as a first line treatment for metastatic melanoma are recruted to the study. Stool samples are submitted before the start of treatment, at the 12 (+/-2) week and 28 (+/-4) week, and at the event ( such as, suspected disease progression/hyperprogressio, immune related adverse event (irAE), etc). Peripheral venous blood samples are taken additionaly at the same time points for cytologic and molecular tests. Histological material from the tumor tissue is obtained before the start of immunotherapy treatment. Primary objectives are to determine whether human gastrointestinal microbiome (bacterial and viral) and exosomal mRNA expression of PD-L1 and IFNγ predict response to treatment with PD-1 and CTLA-4 inhibitors and are associated with occurrence of irAE in patients with metastatic melanoma at different time points. Response is evaluated radiologically with imaging methods in accordance with the irRECIST criteria. Conclussion: Despite the great success of the treatment of metastatic melanoma with immunotherapy, there remains a significant proportion of patients who do not respond to treatment or who develop severe adverse events during treatment. Identification of novel predictive and prognostic biomarkers for immunotherapy treatment response is therefore necessary. This study is the first to combine and investigate multiple potential predictive and prognostic biomarkers and its dynamics. The results could serve for a better and multi-level understanding of the various factors influencing immunotherapy treatment.

Read the detailed description

The goal of this [type of study: observational study or clinical trial] is to [learn about, test, compare etc.] in [describe participant population/health conditions]. The main question[s] it aims to answer are:

  • [question 1]
  • [question 2] Participants will [describe the main tasks participants will be asked to do, treatments they'll be given and use bullets if it is more than 2 items].
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Conditions studied

  • Metastatic Melanoma
  • Immune Checkpoints Inhibitors
  • Gastrointestinal Microbiome (Bacterial and Viral)
  • Exosomal mRNA Expression of PD-L1 and IFNγ

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03

In context

Melanoma

3,073 studies on the registry are indexed under Melanoma; 529 are open to participants now.

This study's planned enrollment of 150 is above the median of 38 across 2,400 interventional studies indexed under Melanoma.

Browse Melanoma studies →

Lead sponsor

Institute of Oncology Ljubljana is the lead sponsor of 90 studies on the registry; 29 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age over 18 years
  • Cytologically or histologically verified malignant melanoma
  • Stage IIID unresectable/IV according to AJCC classification (8th edition, 2018)
  • Performance status according to WHO 0 - 2 (ECOG criteria)
  • 1st line of systemic treatment with immunotherapy (nivolumab, ipi/nivo, pembrolizumab)
  • Triple CT/PET CT done within 4 weeks before the first application
  • Signed consent to participate in clinical research

Exclusion criteria

Exclusion Criteria:

  • Previously treated melanoma with systemic therapy
  • Capacity status according to WHO 3 - 4 (ECOG criteria)
  • Contraindications for immunotherapy treatment (known deficiency of the immune system or active immunosuppressive treatment or active autoimmune disease requiring treatment)
  • Other malignant diseases (except cured basal cell carcinoma and squamous cell carcinoma)
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
150 participants (estimated)

Study arms

  • Other
    Immune checkpoint inhibitors

    Drug: Immune checkpoint inhibitor

Interventions

  • DrugImmune checkpoint inhibitor

    Identification of novel predictive and prognostic biomarkers for immunotherapy treatment response in metastatic melanoma

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What researchers measure

Primary outcomes

  1. response prediction in first line immune checkpoint inhibitors treatment in metastatic melanoma assessed by human gastrointestinal microbiome (bacterial and viral) and exosomal mRNA expression of PD-L1 and IFNγ

    Primary objectives are to determine whether human gastrointestinal microbiome (bacterial and viral) and exosomal mRNA expression of PD-L1 and IFNγ predicts response to treatment with PD-1 and CTLA-4 inhibitors and are associated with occurrence of irAE in patients with metastatic melanoma.

    Time frame: 3 years

07

Study locations

1 of 1 sites recruiting
  • Institute of Oncology Ljubljana
    Ljubljana, Slovenia
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 18, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05878977
Lead sponsor
Institute of Oncology Ljubljana
Collaborators
Blood Transfusion Centre of Slovenia, University Medical Centre Ljubljana, University of Ljubljana
Responsible party
Sponsor
First posted
May 30, 2023
Start date
Oct 5, 2022
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Oct 18, 2024

Study contacts

Tanja Mesti
Contact
tmesti@onko-i.si
0038615879287

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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