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Radiomics and Metabolomics in the Follow-up of CAR T-cells for Refractory or Relapsed Non-Hodgkin's Lymphoma (CART-Omic)

Primary Purpose

Refractory or Relapsed Non-Hodgkin's Lymphoma

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
blood samples and 18FDG PET-CT exams
Sponsored by
Centre Hospitalier Universitaire de Nice
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Refractory or Relapsed Non-Hodgkin's Lymphoma

Eligibility Criteria

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

Inclusion Criteria:

  • Age greater than or equal to 18 years old
  • Patients with histologically proven, refractory or relapsed, non-Hodgkin's lymphoma as indicated for CAR T-cell therapy
  • ECOG score 0 to 2
  • Affiliated patient or beneficiary of a social security scheme
  • Patient having signed prior informed consent.

Exclusion Criteria:

  • Be under 18 years old,
  • Contraindication to performing 18FDG PET-CT examinations: severe claustrophobia, unbalanced diabetes during PET-CT examinations (young capillary blood sugar ≥ 11 mmol),
  • Any participation in other biomedical studies relating to drugs, medical devices or imaging techniques is prohibited, with the exception of so-called non-health product biomedical studies.
  • Hypersensitivity to the active substance or to any of the excipients in the composition of CAR T-cells preparations
  • Pregnant or breastfeeding women

Sites / Locations

  • CHU de NiceRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

identification of predictive and prognostic biomarkers

Arm Description

Outcomes

Primary Outcome Measures

Progression-free survival (PFS) compared and correlated with signatures of the radiomics and serum metabolomics index
Progression-free survival (PFS)

Secondary Outcome Measures

Occurrence of severe side effects compared and correlated with the signatures of the radiomics and serum metabolomics indexes.
occurrence of severe side effects

Full Information

First Posted
May 31, 2022
Last Updated
August 30, 2022
Sponsor
Centre Hospitalier Universitaire de Nice
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1. Study Identification

Unique Protocol Identification Number
NCT05422521
Brief Title
Radiomics and Metabolomics in the Follow-up of CAR T-cells for Refractory or Relapsed Non-Hodgkin's Lymphoma
Acronym
CART-Omic
Official Title
Radiomics and Metabolomics in the Follow-up of CAR T-cells for Refractory or Relapsed Non-Hodgkin's Lymphoma: Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Recruiting
Study Start Date
August 29, 2022 (Actual)
Primary Completion Date
August 29, 2023 (Anticipated)
Study Completion Date
August 29, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Nice

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 an interventionnal pilot study to investigate whether 18FDG radiomics or serum metabolomic signatures could be predictive or prognostic factors in the follow-up of patients receiving CAR T-cell therapy for refractory non-Hodgkin's lymphoma or in relapse.
Detailed Description
In this study the search for relevant radiomic signature will be carried out for each patient benefiting from an 18FDG PET-CT during the pre-treatment assessment and then in the follow-up at 1 month, 3 months, 6 months, 9 months and 12 months post treatment. The search for circulating metabolites in serum (mass spectrometry) will be carried out during the pre-therapeutic assessment, then in the follow-up at 7 days, 1 month, 3 months, 6 months, 9 months and 12 months post treatment. The main objective of the study is the comparison of signatures from radiomics and early serum metabolomic indices according to progression-free survival at 12 months of patients treated with CAR T-cells for refractory or relapsed non-Hodgkin's lymphoma, in correlation with clinical and biological monitoring, to predict tumor response. The secondary objective is the comparison of the signatures of early serum radiomic and metabolic indices according to the occurrence of serious clinical and/or biological side effects in the 12 months following treatment with CAR T cells.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Refractory or Relapsed Non-Hodgkin's Lymphoma

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
identification of predictive and prognostic biomarkers
Arm Type
Experimental
Intervention Type
Other
Intervention Name(s)
blood samples and 18FDG PET-CT exams
Intervention Description
18 FDG PET scanner at inclusion and post CART-cells treatment ( 1, 3, 6, 9 and 12 month) blood collection at inclusion and post CART-cells treatment (7 days, 1 month and 3 month)
Primary Outcome Measure Information:
Title
Progression-free survival (PFS) compared and correlated with signatures of the radiomics and serum metabolomics index
Description
Progression-free survival (PFS)
Time Frame
7 days, 1 month, 3 months, 6 months, 9 months and 12 months post treatment.
Secondary Outcome Measure Information:
Title
Occurrence of severe side effects compared and correlated with the signatures of the radiomics and serum metabolomics indexes.
Description
occurrence of severe side effects
Time Frame
7 days, 1 month, 3 months, 6 months, 9 months and 12 months after injection

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age greater than or equal to 18 years old Patients with histologically proven, refractory or relapsed, non-Hodgkin's lymphoma as indicated for CAR T-cell therapy ECOG score 0 to 2 Affiliated patient or beneficiary of a social security scheme Patient having signed prior informed consent. Exclusion Criteria: Be under 18 years old, Contraindication to performing 18FDG PET-CT examinations: severe claustrophobia, unbalanced diabetes during PET-CT examinations (young capillary blood sugar ≥ 11 mmol), Any participation in other biomedical studies relating to drugs, medical devices or imaging techniques is prohibited, with the exception of so-called non-health product biomedical studies. Hypersensitivity to the active substance or to any of the excipients in the composition of CAR T-cells preparations Pregnant or breastfeeding women
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Philippe VIAU, MD
Phone
0492035672
Email
viau.p@chu-nice.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Mickael LOSCHI, MD
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philippe VIAU
Organizational Affiliation
Centre Hospitalier Universitaire de Nice
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU de Nice
City
Nice
ZIP/Postal Code
06000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Valérie Foussat
First Name & Middle Initial & Last Name & Degree
Philippe VIAU, MD
First Name & Middle Initial & Last Name & Degree
Mickael LOSCHI, MD

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Radiomics and Metabolomics in the Follow-up of CAR T-cells for Refractory or Relapsed Non-Hodgkin's Lymphoma

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