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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02853214
Other study ID # 2007-460
Secondary ID 2007-A00644-49
Status Completed
Phase N/A
First received
Last updated
Start date February 6, 2008
Est. completion date September 25, 2023

Study information

Verified date February 2023
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Multiple Myeloma (MM) is a malignant proliferation of monoclonal plasma cells. Myeloma accounts for almost 14% of all hematologic cancers and is essentially incurable. Myeloma commonly evolves from a precursor disease, Monoclonal gammopathy of undetermined significance (MGUS). Despite intensive study, the etiology of MGUS and myeloma are unknown and no lifestyle or environmental exposure factors have been identified that are consistently linked to increased risk of MM, MGUS or the transition between the two. The overall goal is to identify risk genes for dysglobulinemia, and more specifically Multiple Myeloma. This will involve the conservation of cells in a bank and genetic sequencing on samples obtained from families with at least two cases of dysglobulinemia. Material used for sequencing is likely to include fresh peripheral blood cells or lymphoblastoid lines established from peripheral blood lymphocytes of patients.


Recruitment information / eligibility

Status Completed
Enrollment 1868
Est. completion date September 25, 2023
Est. primary completion date September 25, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - 2 cases per family at least - 1 case alive at least - biological material available for 1 case at least - Patients give their informed consent - attached to the French Health protection service Exclusion Criteria: - Age under 18

Study Design


Related Conditions & MeSH terms


Intervention

Genetic:
Genetic analysis of peripheral blood samples
M.D investigators report the identified families with all the information: description of the familial area (for example: 2 cases father and son), last medical report for the case with the type of dysglobulinemia, monoclonal component isotype, medical background and contact information for one of the patients or cases with Name/surname/Date of Birth/address and phone. They contact the patient to explain the study and establish the family pedigree. They collect the information on all the family members and send to the patient a mail: an information note on the study, a prescription for the blood sample and the informed consents. They proceed in the same way for the relatives with the additional prescription: EIP. They organize the logistic in the medical lab or hospital chosen by the person. They receive 4 Heparin and 1 serum tubes for each and with this, they obtain a large amount of biological material for the genetic analysis thanks to the establishment of lymphoblastoid cell lines

Locations

Country Name City State
France CHU d'ABBEVILLE Abbeville
France CHU Amiens Picardie Amiens
France CHU Groupe Hospitalier Sud Hématologie Clinique Amiens
France CH d'Avignon Avignon
France CHU de Besançon Besançon
France CH de Blois Service d'Hématologie Blois
France Hôpital Avicenne Service d'Hématologie Bobigny
France Service d'Hématologie clinique et Thérapie Cellulaire, CHU de BORDEAUX Bordeaux
France CHU Morvan Brest
France Service d'hématologie Clinique Caen
France Hématolgie- Hôpital privé Cesson-Sévigné Cesson-Sévigné
France CH William Morey, Service d'Hémato-Oncologie Chalon-sur-Saône
France CHU de Chartres Chartres
France Département d'Oncogénitique - Centre Jean Perrin Clermont-Ferrand
France Hôpital Sud Francilien Corbeil-Essonnes
France Service d'Hématologie Clinique, CHU de Dijon Dijon
France Centre Hospitalier de Dunkerque Dunkerque
France Service de Médecine Interne-Hématologie, CHU de Fort de France Fort de France Fort-de-France Martinique
France CHU Albert Michallon Grenoble
France GHM, Institut Daniel Hollard Grenoble
France Service d'Hématologie, CHU de Versailles Le Chesnay
France Centre Jean Bernard Clinique Victor Hugo Le Mans
France Service d'Onco-hématologie, Hôpital Saint-Vincent GH-ICL Lille
France Service des Maladies du Sang CHU Lille Lille
France Département d'Oncogénétique, Centre Paoli Calmettes Marseille
France CHR-Metz-Thionville, Hôpital de Mercy, Service d'Hématologie Metz
France CHU d'Annecy Metz-Tessy
France Hôpital Saint-Eloi, Département d'Hématologie clinique Montpellier
France Service d'Oncologie Médical, Centre Azuréen de Canrérologie-1 Mougins
France CHU-HÔTEL -Dieu de Nantes Nantes
France Hôpital de l'Archet 1 Nice
France CHU Carémeau Nîmes
France Hôpital St Antoine Service des maladies du Sang Paris
France Institut Curie Paris
France Jean Paul FermandService Immuno-Hématologie Hôpital Saint Louis Paris
France Hospices Civils de Lyon Pierre Benite
France Service d'Oncologie-Radiothérapie - CHU Pointe-à-Pitre/Abymes Guadeloupe POINTE-à-PITRE Guadeloupe
France CHU de Poitiers Poitiers
France Hôpital Robert Debré Service du Professeur A. DELMER Hématologie Clinique Reims
France CHU de Rennes Hôpital Sud Rennes
France CH de Rodez Rodez
France Hôpital de Saint- Germain en Laye Saint-Germain-en-Laye
France Département d'Hématologie à l'Institut de Cancérologie de la Loire Saint-Priest-en-Jarez
France Hôpital Purpan Service d'Hématologie Toulouse
France Centre Hospitalier de Valence Valence
France CHU de Nancy, Hôpital de Brabois Vandœuvre-lès-Nancy
France Hôpital Privé de Villeneuve d'Ascq Villeneuve d'Ascq

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Data of a bank cells, clinically annotated, from families with at least 2 cases of dysglobulinemia and at least 1 case alive.plasma cell dysplasia The investigator collects blood samples from patients with dysglobulinemia and their relatives and with this, the investigators constitutes the bank cells thanks to the establishment of lymphoblastoid cell lines.
The investigator considers as "dysglobulinemia" cases patients with Multiple Myeloma, MGUS, Waldenström's disease and MGUS (monoclonal gammopathy of unknown significance ) as wells as plasmacytomas confirmed histologically or cytologically.
up to 48 months
Secondary Single Nucleotide Polymorphism array for identification of polymorphisms predictive of dysglobulinemia The biological material, obtained from fresh peripheral blood cells and from Lymphoblastoid cells lines, is used for pangenic sequencing. It allows to better understand the mechanism of genetic variations who could be involve in the myeloma genesis at day 0