ANRS CO16: Cohort of HIV Associated Lymphomas

Sponsor
ANRS, Emerging Infectious Diseases (Other)
Overall Status
Completed
CT.gov ID
NCT01164436
Collaborator
Dr Yassine Taoufik Dr Houria Chavez Hôpital Bicêtre CIB Paris Sud France (Other), Dr Guislaine Garcelain Hôpital Pitié Slapétrière Paris France (Other), University Hospital, Grenoble (Other), Dr Irène Joab Hôpital Paul Brousse Villejuif France (Other), Dr Alex Duval Fondation Jean Dausset CEPH (Other), Hopital Antoine Beclere (Other)
205
1
108
1.9

Study Details

Study Description

Brief Summary

The incidence of lymphomas is increased among HIV infected patients. In 70 % of cases, those are Non Hodgkin's lymphomas (NHL) and Hodgkin lymphomas (HL) in 30% of cases. In France, their incidence is estimated to 100 cases per year (data from the "Base de données Hospitalière Française sur l'Infection à VIH" (FHDH)). The main mechanisms involved in lymphomagenesis are immune dysfunction, involvement of oncogenic viruses (Epstein-Barr (EBV) and HHV8) and molecular oncogenic events. A better understanding of these different pathways, give the possibility to design specific treatments. The treatment of these lymphomas is not standardized. A prospective study of patients with HIV associated lymphoid malignancies is an innovating tool to answer epidemiological, physiopathological and therapeutic questions. We propose a prospective multicentric study of these patients.

The main objectives of this prospective study are to:
  • evaluate the incidence, characterise clinically and histologically NHL and HL cases associated to HIV

  • perform an observational study of the treatment and outcome of these patients out of the context of clinical trials,

  • study the differentiation and activation of B-cell populations,

  • better understand the role of specific T cell responses in the control of EBV infection,

  • allow other biological studies from the ANRS group " Lymphome et VIH ".

The recruitment of 40 cases per year is expected. The length of inclusions is 7 years. The follow-up will be of 2 years. Clinical, pathological and biological data at diagnosis and during follow-up will be collected. This will allow characterizing the lymphoma, the HIV infection, the antitumoral treatments and the outcome of lymphoma. Biological samples will be centralized to collect cell, DNA, RNA, plasma, serum and tumour collections (Y.Taoufik, S Prevot* ). To better understand the EBV infection and lymphomagenesis in HIV infection, we propose to follow the viral load and the molecular characteristics of EBV in PBMC, plasma and tumour (P.Morand* , V.Boyer* ), to investigate the EBV-T cell responses (G.Carcelain) and the presence and reactivation of EBV in peripheral B cells (C.Amiel* , JC Nicolas) and in tumoral samples (M.Raphael* , I.Joab* ). The other mechanisms of lymphomagenesis in HIV infection will be studied by the analysis of the sub-populations of B-cells in terms of activation and differentiation (Y.Taoufik) and by the characterization of MSI tumours (A.Duval).

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    205 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    French Cohort of HIV Associated Lymphomas
    Study Start Date :
    Jun 1, 2008
    Actual Primary Completion Date :
    Jun 1, 2015
    Actual Study Completion Date :
    Jun 1, 2017

    Outcome Measures

    Primary Outcome Measures

    1. Correlation between EBV viral load and plasma HIV RNA viral load and CD4 cell count in HIV-infected patients with lymphomas (LNH or LH) at the time of lymphoma diagnosis [5 year]

    Secondary Outcome Measures

    1. Survival rate in HIV patients with NHL or HL [5 year]

    2. Progression-free survival rate in HIV patients with NHL or HL [5 year]

    3. Levels of EBV in tumors of HIV patients with NHL or HL [5 year]

      measurement of EBV using in situ hybridization applied to paraffin sections

    4. Levels of B cell activating cytokines in plasma of HIV patients with NHL or HL [5 year]

      measurement of concentrations of IL-6, IL-10, BAFF in plasma

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Male and female patients over 18 years of age

    • patients with HIV-1 or 2 infection

    • with Non Hodgkin's lymphomas (NHL) or Hodgkin lymphomas (HL) in the diagnosis or in relapse

    • sign an informed consent

    Exclusion Criteria:
    • patients who suffered from acute leukemia

    • patients treated for lymphoïd blood disease

    • Patients whose lymphomas treatment was stopped for less than 3 months

    • unaffiliated to the social healthy security french system

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 BESSON Paris France

    Sponsors and Collaborators

    • ANRS, Emerging Infectious Diseases
    • Dr Yassine Taoufik Dr Houria Chavez Hôpital Bicêtre CIB Paris Sud France
    • Dr Guislaine Garcelain Hôpital Pitié Slapétrière Paris France
    • University Hospital, Grenoble
    • Dr Irène Joab Hôpital Paul Brousse Villejuif France
    • Dr Alex Duval Fondation Jean Dausset CEPH
    • Hopital Antoine Beclere

    Investigators

    • Principal Investigator: Caroline BESSON, Service Hématologie Immunologie Biologie, Hopital Bicetre
    • Principal Investigator: Gilles Pialoux, PH, Hôpital Tenon Paris
    • Principal Investigator: Marie Caroline Meyonas, PH, Hôpital St Antoine Paris
    • Principal Investigator: Christine Katlama, PH, Hôpital Pitiè Salpétrière
    • Principal Investigator: Jean Gabarre, MD, Hôpital Pitiè Salpétrière Paris
    • Principal Investigator: Dominique Salmon, PH, Hôpital Cochin PARIS
    • Principal Investigator: François Dreyfus, PH, Hôpital Cochin Paris
    • Principal Investigator: Jean Paul Viard, PH, Hotel Dieu PARIS
    • Principal Investigator: Alain Devidas, PH, Corbeil Essone 91
    • Principal Investigator: Emma Goldschmidt, MD, Villejuif 94
    • Principal Investigator: Cecile Goujard, MD, Hôpital Bicêtre 94
    • Principal Investigator: Laurent Blum, MD, Pointoise 95
    • Principal Investigator: François Boué, PH, Clamart 92
    • Principal Investigator: Eric Rosenthal, MD, Nice 06
    • Principal Investigator: Christine Burty, MD, Vandoeuvre les Nancy 54
    • Principal Investigator: Jean Marie Lang, PH, Strasbourg 67
    • Principal Investigator: Renaud Verdon, PH, Caen 14
    • Principal Investigator: Yazdan Yazdanpanah, PH, Tourcoing 59
    • Principal Investigator: Christine Drobacheff, MD, Besancon 25
    • Principal Investigator: Bruno Marchou, PH, Toulouse 31
    • Principal Investigator: Corinne Couteau, MD, Toulouse 31
    • Principal Investigator: Philippe Morlat, PH, Bordeaux 33
    • Principal Investigator: Christian Trepo, PH, Lyon 69
    • Principal Investigator: Hervé Ghesquières, PH, Lyon 69
    • Principal Investigator: Régis Costellos, PH, Marseille
    • Principal Investigator: Bertrand Coiffier, Ph, Pierre Bénite
    • Principal Investigator: Claude Beuscart, MD, St Brieuc 22
    • Principal Investigator: Philippe Perre, MD, La Roche Sur Yon 85
    • Principal Investigator: Patrice Poubeau, MD, St Pierre 97
    • Principal Investigator: François Raffi, PH, Nantes 44
    • Principal Investigator: Frédéric Lucht, PH, St Etienne 42
    • Principal Investigator: Nicolas Mounier, PH, Nice 06
    • Principal Investigator: Cédric Arvieux, PH, Rennes 35
    • Principal Investigator: Serge Herson, PH, Pitié Salpétrière Paris
    • Principal Investigator: Jean François Bergmann, PH, Lariboisière Paris
    • Principal Investigator: André Cabié, PH, Fort de France 97( Martinique)

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    ANRS, Emerging Infectious Diseases
    ClinicalTrials.gov Identifier:
    NCT01164436
    Other Study ID Numbers:
    • 2007-AO0258-45
    First Posted:
    Jul 16, 2010
    Last Update Posted:
    Nov 6, 2017
    Last Verified:
    Oct 1, 2017
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 6, 2017