DeLPHy: Screening for Oculocerebral Lymphoma With the Phenotype of NK Cells in Patients With Uveitis

Sponsor
Hospices Civils de Lyon (Other)
Overall Status
Recruiting
CT.gov ID
NCT05388838
Collaborator
(none)
45
2
5
12
22.5
1.9

Study Details

Study Description

Brief Summary

Uveitis is an inflammation of the uvea, an ocular tunic comprising the iris, ciliary body and choroid. This inflammation can also involve other tissues such as the retina, the optic nerve and the aqueous humor. These diseases can result in significant vision loss and account for 10% of all blindness in developed countries, and up to 25% in developing countries. The main difficulty in this pathology is to make the etiological diagnosis, which then allows a specific treatment of the disease. The main etiologie are inflammatory or infectious (sarcoidosis, tuberculosis) but other cancerous etiologies are possible and are of more complicated diagnosis.

Vitreoretinal lymphoma is a subtype of central nervous system lymphoma, which is generally associated with a poor prognosis. It is a diffuse non-Hodgkin's lymphoma, with large B cells. It can be primary ocular (Primary Intra-Ocular Lymphoma - LIOP), without brain involvement, but can also be secondary to central nervous system involvement, which explains the poor prognosis of the disease. Approximately 50-90% of LIOP develop brain involvement within 1-2 years of diagnosis, which encourages early diagnosis to avoid brain involvement as much as possible.

The main obstacle to rapid diagnosis is the difficulty of identifying LIOP. Indeed, the clinical symptoms of this rare disease are often identical to classical uveitis, and the diagnostic means to detect it are invasive and require a trained ophthalmologist and hematologist team. LIOP diagnostic tests are often delay in the management of uveitis and lead to diagnostic erraticity that can last between 4 to 40 months.

The INSERM U1183 unit is developing a diagnostic technology for lymphomas based on the analysis of blood NK cells and their phenotypes including those acquired by trogocytosis (WO/2016/005548).

A rapid, simple, minimally invasive LIOP test using this technology could therefore be propose to all patients presenting with uveitis and whose clinical criteria could match those of LIOP.

The research hypothesis is : Could the diagnostic wandering of patients with primary intraocular lymphoma be reduced by a rapid blood test for NK cell phenotype of patients with uveitis? Following a simple blood test, a rapid LIOP test, using this diagnostic technology, could therefore be proposed to all patients with uveitis and clinical criteria (age, intermediate and posterior location of the uveitis) corresponding to those of LIOP.

The primary objective of this study is to compare the phenotype of circulating NK cells of patient with untreated intraocular lymphoma versus the phenotype of patient with non-cancerous uveitis.

Condition or Disease Intervention/Treatment Phase
  • Biological: Blood sample
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
45 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Prospective Case Control StudyProspective Case Control Study
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Screening for Oculocerebral Lymphoma by Identifying the Phenotype Carried by Circulating NK Cells in Patients With Uveitis
Actual Study Start Date :
Jun 1, 2022
Anticipated Primary Completion Date :
Jun 1, 2023
Anticipated Study Completion Date :
Jun 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Negative control

uveitis patients with a diagnosis other than ocular diagnosis other than ocular lymphoma and without cerebral lymphoma (15 patients),

Biological: Blood sample
Blood sample will be taken at D0: 63 ml (7 tubes of 9 ml),

Active Comparator: Primary ocular Lymphoma without brain involvementand never treated

patients with primary ocular lymphoma without brain involvement and never treated (5 patients),

Biological: Blood sample
Blood sample will be taken at D0: 63 ml (7 tubes of 9 ml),

Active Comparator: Primary ocular Lymphoma without brain involvement and treated

patients with primary ocular lymphoma without brain involvement, treated and considered in remission (5 patients),

Biological: Blood sample
Blood sample will be taken at D0: 63 ml (7 tubes of 9 ml),

Active Comparator: Primary ocular Lymphoma without brain involvement in relapse

patients with primary ocular lymphoma without brain involvement, considered in relapse (5 patients),

Biological: Blood sample
Blood sample will be taken at D0: 63 ml (7 tubes of 9 ml),

Active Comparator: Positive control

patients with cerebral lymphoma without ocular involvement and without uveitis (15 patients).

Biological: Blood sample
Blood sample will be taken at D0: 63 ml (7 tubes of 9 ml),

Outcome Measures

Primary Outcome Measures

  1. percentage of NK Cells in blood with phenotype acquired by trogocytosis (WO/2016/005548) in patients with uveitis with a diagnosis other than ocular lymphoma and without cerebral lymphoma (Negative control) [through study completion, an average of 1 year]

    mesure by Flow Cytometry

  2. percentage of NK Cells in blood with phenotype acquired by trogocytosis (WO/2016/005548) in patients with primary ocular lymphoma without brain involvement and never treated [through study completion, an average of 1 year]

    mesure by Flow Cytometry

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

GENERAL CRITERIA

  • Male or female over 40 years of age,

  • Free, informed, written consent signed by the patient and the investigator (at the latest on the day of inclusion) and before any examination required by the research,

  • Patient affiliated to the social security system or beneficiary of such a system,

  • Maximum volume of sampling (care + research) per 30-day period to be adapted according to the patient's weight (Order of April 12, 2018 establishing the list of research mentioned in 2° of Article L. 1121-1).

SPECIFIC CRITERIA

  • Patient affected in one or both eyes: of uveitis with another diagnosis than ocular lymphoma and without cerebral lymphoma (Group 1), or primary ocular lymphoma without brain involvement and never treated (Group 2), or primary ocular lymphoma without brain involvement, treated and considered in remission (IL10 HA level < 10) (Group 3), or primary ocular lymphoma without brain involvement, and considered in relapse (IL10 HA level > 30) (Group 4), or cerebral lymphoma without ocular involvement and without uveitis (Group 5).
Exclusion Criteria:
  • -GENERAL CRITERIA

  • Patient participating in an ongoing clinical trial at the time of the inclusion visit,

  • Pregnant women, women in labor or nursing mothers,

  • Persons deprived of liberty by a judicial or administrative decision,

  • Persons under psychiatric care,

  • Persons admitted to a health or social institution for purposes other than research,

  • Persons of full age who are subject to a legal protection measure (guardianship, curatorship).

SPECIFIC CRITERIA

  • Patient for whom the diagnosis of ocular or cerebral lymphoma is uncertain,

  • Patient with another systemic cancer that is evolving or in remission < 2 years.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Service d'Ophtalmologie, Hôpital de la Croix-Rousse, GHN Lyon France 69004
2 Service d'Hématologie Clinique, Hôpital Lyon Sud Lyon France 69310

Sponsors and Collaborators

  • Hospices Civils de Lyon

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hospices Civils de Lyon
ClinicalTrials.gov Identifier:
NCT05388838
Other Study ID Numbers:
  • 69HCL22_0078
First Posted:
May 24, 2022
Last Update Posted:
Jun 13, 2022
Last Verified:
Jun 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 13, 2022