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Biomarkers in Immunotherapy of Melanoma

Primary Purpose

Metastatic Melanoma, Immune Checkpoints Inhibitors, Gastrointestinal Microbiome (Bacterial and Viral)

Status
Recruiting
Phase
Not Applicable
Locations
Slovenia
Study Type
Interventional
Intervention
Immune checkpoint inhibitor
Sponsored by
Institute of Oncology Ljubljana
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metastatic Melanoma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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: 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)

Sites / Locations

  • Institute of Oncology LjubljanaRecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Immune checkpoint inhibitors

Arm Description

Outcomes

Primary Outcome Measures

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.

Secondary Outcome Measures

Full Information

First Posted
April 19, 2023
Last Updated
May 17, 2023
Sponsor
Institute of Oncology Ljubljana
Collaborators
University of Ljubljana, Military Medical Academy, Belgrade, Serbia
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1. Study Identification

Unique Protocol Identification Number
NCT05878977
Brief Title
Biomarkers in Immunotherapy of Melanoma
Official Title
Effectiveness of Immunotherapy in the First-line Treatment of Disseminated Melanoma and Recognition of Prognostic and Predictive Biomarkers From the Primary Tumor, Stool and Body Fluids: PROTOCOL TRIAL
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 5, 2022 (Actual)
Primary Completion Date
December 31, 2026 (Anticipated)
Study Completion Date
December 31, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institute of Oncology Ljubljana
Collaborators
University of Ljubljana, Military Medical Academy, Belgrade, Serbia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metastatic Melanoma, Immune Checkpoints Inhibitors, Gastrointestinal Microbiome (Bacterial and Viral), Exosomal mRNA Expression of PD-L1 and IFNγ

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Immune checkpoint inhibitors
Arm Type
Other
Intervention Type
Drug
Intervention Name(s)
Immune checkpoint inhibitor
Intervention Description
Identification of novel predictive and prognostic biomarkers for immunotherapy treatment response in metastatic melanoma
Primary Outcome Measure Information:
Title
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
Description
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

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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: 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)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tanja Mesti
Phone
0038615879287
Email
tmesti@onko-i.si
Facility Information:
Facility Name
Institute of Oncology Ljubljana
City
Ljubljana
Country
Slovenia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tanja Mesti
Phone
+38615879287
Email
tmesti@onko-i.si

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Biomarkers in Immunotherapy of Melanoma

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