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Relationship Between Immunity and Metabolism in Patients Receiving Immune Checkpoint Inhibitors for Advanced Cancer. ( RIMEC )

A

Assistance Publique - Hôpitaux de Paris

Status

Active, not recruiting

Conditions

Immune Checkpoint Inhibitors
Cancer
Metabolism Disorder

Treatments

Diagnostic Test: calorimetry, impedance measurement at baseline and after 3 months of treatment

Study type

Interventional

Funder types

Other

Identifiers

NCT04808817
IDRCB 2020-A02262-37 (Other Identifier)
APHP201166

Details and patient eligibility

About

Recent EMA and FDA approvals have made immune checkpoint inhibitors (ICI) a standard of care in cancer treatment. ICI, used alone or as a combination are now the backbone of renal cell and lung carcinoma treatment. However, a significant proportion of patients does not respond to ICI. Thus the identification of predictive response factor is a major issue.

While factors associated with the tumour and its micro environment have been widely studied, factors associated with the patient such as metabolism could also affect the response to ICI and remain poorly studied.

The hypothesis of the investigators is that dysmetabolims, via the induction of a chronic inflammatory state could induce a defect of lymphocyte production and activation as well as a modification of the immunogenicity of tumor cells and immune cells infiltration. The consequences could be a decrease in ICI response rate as well as an increase in immune related adverse events (irAEs).

To test this hypothesis, the investigators propose a prospective bi-centric exploratory study including 60 patients treated with ICI for advanced lung or renal cell carcinoma.

The data collected will be :

  • Clinical (calorimetry, impedancemetry, survey of eating habits, tumour characteristics, epidemiological data),
  • Biologics (baseline and 3-months plasma bio banking for standard biology, inflammation markers TNF- α, IL1-6-8-11-17, TGF-ß, TWEAK, complement study C3, C4, C4d, CH50, C1q, CD46)

Primary objective is to assess the response to ICI depending on metabolic status.

Secondary objectives are to study the relationships between metabolism / cytokines profile/ complement profile and ICI response.

The investigators seek to generate hypotheses and to obtain exploratory data before submission of a Hospital Clinical Research Program whose objective will be to evaluate the impact of dysmetabolism on overall survival and to characterize immune and anatomopathological profiles (using DNA microarrays and flow cytometry techinques) of patients treated with ICI for renal cell or lung carcinoma.

Enrollment

48 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients ≥18 years
  • patients receiving immune checkpoint inhibitors, used alone or as a combination with chemotherapy or tyrosine kinase inhibitor or other immune checkpoint inhibitor, for advanced renal cell or lung carcinoma.
  • Patient Informed and signed the consent to participate in the research

Exclusion criteria

  • patients with history of auto immune disease
  • patients enrolled in an interventional study or be in the exclusion period following a previous research, if applicable
  • Patient not affiliated to the social security scheme or under AME
  • Patient under guardianship or curatorship or under legal protection
  • Patient unable or unwilling to give written consent
  • Pregnant patient

be in the exclusion period following a previous research, if applicable

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

48 participants in 1 patient group

patients
Experimental group
Treatment:
Diagnostic Test: calorimetry, impedance measurement at baseline and after 3 months of treatment

Trial contacts and locations

2

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Central trial contact

LE MAO Laura, Msc; SIMONAGGIO Audrey, MD

Data sourced from clinicaltrials.gov

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