Back to resultsImmunological Variables Associated to ICI Toxicity in Cancer Patients
Primary Purpose
Breast Cancer, Melanoma, Non Small Cell Lung Cancer
Status
Recruiting
Phase
Phase 2
Locations
Belgium
Study Type
Interventional
Intervention
Checkpoint Blockade, Immune
Sponsored by
About this trial
This is an interventional other trial for Breast Cancer
Eligibility Criteria
Inclusion Criteria:
- 1) Age ≥ 18 years old
- 2) ECOG performance status ≤ 1
- 3) Must have histologically or cytologically confirmed solid tumour, eligible for treatment with ICI as standard-of-care alone or in combination with another ICI (cohort 1), ICI with chemotherapy (cohort 2), or ICI with targeted therapy (cohort 3) with no restrictions on number of prior systemic therapies
- 4) All prior anti-cancer treatment-related toxicities (except alopecia) must be ≤ Grade 1 according to the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 at the time of enrolment
- 5) Serum pregnancy test (for subjects of childbearing potential) negative within 15 days prior to study medications administration.
- 6) Women of childbearing potential must agree to use one highly effective method of contraception prior study entry, during the course of the study and at least 7 months after the last administration of study treatments.
- 7) Men with childbearing potential partner must agree to use condom during the course of this study and for at least 6 months after the last administration of the study treatments.
- 8) Completion of all necessary screening procedures within 14 days prior to enrolment.
- 9) Signed Informed Consent form (ICF) obtained prior to any study related procedure.
Exclusion Criteria:
Subjects meeting one of the following criteria are not eligible for this study:
- Subject with a significant medical, neuro-psychiatric, or surgical condition, currently uncontrolled by treatment, which, in the principal investigator's opinion, may interfere with completion of the study.
- Participation in another clinical trial.
- Pregnant and/or lactating women.
- Subjects already receiving ICI.
Sites / Locations
- Institut Jules BordetRecruiting
Outcomes
Primary Outcome Measures
Modification(s) in the immune blood markers of treated subjects on treatment.
Modification(s) in the immune blood markers including cytokines, immune cells and serum autoantibody level of treated subjects.
Modification(s) in the immune blood markers of treated subjects on treatment.
Modification(s) in the immune blood markers including cytokines, immune cells and serum autoantibody level of treated subjects.
Modification(s) in the immune blood markers of treated subjects on treatment.
Modification(s) in the immune blood markers including cytokines, immune cells and serum autoantibody level of treated subjects.
Modification(s) in the immune blood markers of treated subjects on treatment at the occurence of any grade 1 or 2 irAE.
Safety will be assessed and graded by the investigator(s) by using the adverse events reported during the study in accordance with the National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0.
Modification(s) in the immune blood markers of treated subjects on treatment at the occurence of any grade 3 or 4 irAE.
Safety will be assessed and graded by the investigator(s) by using the adverse events reported during the study in accordance with the National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05429866
Brief Title
Immunological Variables Associated to ICI Toxicity in Cancer Patients
Official Title
Immunological Variables Associated to ICI Toxicity in Cancer Patients
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2022 (Actual)
Primary Completion Date
June 1, 2024 (Anticipated)
Study Completion Date
December 1, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Jules Bordet Institute
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a monocentric, prospective, pilot study that will enrol 435 subjects with solid tumours that are treated with immune checkpoint inhibitor(s) (ICI) alone or in combination with chemotherapy or targeted therapy.
For enrolled subjects, clinical and laboratory evaluations will be performed and reported at different time points:
Early (4-6 weeks after treatment start)
Midtime (8-11 weeks after treatment start)
Late (13-18 weeks after treatment start)
At the occurrence of immune-related adverse events (irAEs), clinical and laboratory evaluation will be performed at two principal time points:
For the 1st time of any grade 1 or 2 irAE if the subject developed it.
For the 1st time of any grade 3 or 4 irAE if the subject developed it.
Detailed Description
Advances in treating patients with immunotherapy has dramatically changed cancer morbidity and mortality. Immune checkpoint inhibitors (ICI), alone or combined with other drugs, are currently used both as standard of care or in experimental settings for various cancers. Currently, ICI treatment induces objective clinical responses in 20-40% of patients, which varies by tumour type. A significant risk of immune-related adverse events (irAE) is also associated with ICI treatment, including the onset of autoimmune diseases. While the incidence of irAE is highly variable and influenced by many factors, phase I and II trials reported rates from 10% to 80% for any grade irAE while an irAE of grade 3 or higher was observed in 2.5% to 18% of subjects. Despite the fact that older adults represent the growing majority of patients diagnosed with cancer, the efficacy and toxicity of ICI in older patients, alone or in combination with other agents, remains controversial. Presently, the specific immune mechanism(s) driving irAE are unknown and biomarkers that predict their onset, particularly high-grade irAE, are urgently needed. The identification of predictive clinical, laboratory and immunological biomarkers (blood and tissue) for toxicity will more accurately identify and quantify patients who are at risk for ICI therapy. Then, this will possibly allow better irAE management.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Melanoma, Non Small Cell Lung Cancer, Non-melanoma Skin Cancer, Gastrointestinal Cancer, Head and Neck Cancer, Renal Cell Carcinoma, Small Cell Lung Cancer, Mesothelioma, Malignant, Bladder Cancer, Merkel Cell Carcinoma, Hepatocellular Carcinoma, MSI-H Colorectal Cancer
7. Study Design
Primary Purpose
Other
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Model Description
This is a monocentric, prospective, pilot study that will enrol 435 subjects with solid tumours that are treated with immune checkpoint inhibitor(s) (ICI) alone or in combination with chemotherapy or targeted therapy.
Masking
None (Open Label)
Allocation
N/A
Enrollment
441 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Checkpoint Blockade, Immune
Other Intervention Name(s)
Ipililumab, Nivolumab, Pembrozilumab, atezolizumab, avelumab, durvalumab, Cemiplimab
Intervention Description
Immune checkpoint blockade drugs target the immune system by blocking control pathways regulating anti-tumor immunity and thereby reinvigorate their activities against cancer.
Primary Outcome Measure Information:
Title
Modification(s) in the immune blood markers of treated subjects on treatment.
Description
Modification(s) in the immune blood markers including cytokines, immune cells and serum autoantibody level of treated subjects.
Time Frame
Assessment: between week 4 and 6 after the first dose of the treatment
Title
Modification(s) in the immune blood markers of treated subjects on treatment.
Description
Modification(s) in the immune blood markers including cytokines, immune cells and serum autoantibody level of treated subjects.
Time Frame
Assessment: between week 8 and 11 after the first dose of the treatment
Title
Modification(s) in the immune blood markers of treated subjects on treatment.
Description
Modification(s) in the immune blood markers including cytokines, immune cells and serum autoantibody level of treated subjects.
Time Frame
Assessment: between week 13-18 after the first dose of the treatment
Title
Modification(s) in the immune blood markers of treated subjects on treatment at the occurence of any grade 1 or 2 irAE.
Description
Safety will be assessed and graded by the investigator(s) by using the adverse events reported during the study in accordance with the National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0.
Time Frame
Assessment: Day1 after diagnostic of any grade 1 or 2 irAE
Title
Modification(s) in the immune blood markers of treated subjects on treatment at the occurence of any grade 3 or 4 irAE.
Description
Safety will be assessed and graded by the investigator(s) by using the adverse events reported during the study in accordance with the National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0.
Time Frame
Assessment: Day one after diagnostic of any grade 3 or 4 irAE
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
1) Age ≥ 18 years old
2) ECOG performance status ≤ 1
3) Must have histologically or cytologically confirmed solid tumour, eligible for treatment with ICI as standard-of-care alone or in combination with another ICI (cohort 1), ICI with chemotherapy (cohort 2), or ICI with targeted therapy (cohort 3) with no restrictions on number of prior systemic therapies
4) All prior anti-cancer treatment-related toxicities (except alopecia) must be ≤ Grade 1 according to the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 at the time of enrolment
5) Serum pregnancy test (for subjects of childbearing potential) negative within 15 days prior to study medications administration.
6) Women of childbearing potential must agree to use one highly effective method of contraception prior study entry, during the course of the study and at least 7 months after the last administration of study treatments.
7) Men with childbearing potential partner must agree to use condom during the course of this study and for at least 6 months after the last administration of the study treatments.
8) Completion of all necessary screening procedures within 14 days prior to enrolment.
9) Signed Informed Consent form (ICF) obtained prior to any study related procedure.
Exclusion Criteria:
Subjects meeting one of the following criteria are not eligible for this study:
Subject with a significant medical, neuro-psychiatric, or surgical condition, currently uncontrolled by treatment, which, in the principal investigator's opinion, may interfere with completion of the study.
Participation in another clinical trial.
Pregnant and/or lactating women.
Subjects already receiving ICI.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
mireille Langouo Fontsa, MD
Phone
0032 (0) 484729928
Email
mireille.langouo@bordet.be
Facility Information:
Facility Name
Institut Jules Bordet
City
Brussel
State/Province
Anderlecht
ZIP/Postal Code
1070
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
MIREILLE LANGOUO, MD, PhD
Phone
0032(2)5413377
Email
mireille.langouo@bordet.be
12. IPD Sharing Statement
Plan to Share IPD
No
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Immunological Variables Associated to ICI Toxicity in Cancer Patients
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