Among all MM patients included in the cohort at the time of diagnosis of SARS-CoV-2 infection, blood samples will be collected at inclusion, at time of the infection acute phase in the most severe cases (when admitted in intensive care units), and at recovery. The following immune function tests will be evaluated, gammaglobulin measurements, lymphocytes counts, B, T, and NK cells analyses by cytometry, including exhaustion analyses. In addition, T cell repertoire sequencing looking for SARS-CoV-2- specific T cells, and serologies, will be evaluated at recovery and 6 months after MM treatment re-initiation.
MM is a hematological malignancy, supposed mainly not curable, except for some exceptional patients, despite the availability of numerous new drugs. The patients are highly susceptible to infections, both bacterial and viral, due to a defect immune status, both at the antibody level (hypogammaglobulinemia) and the cellular level. This immunosuppression is further worsened by the treatments, and especially high dose glucocorticoids used at each phase of the disease. Consequently, MM patients are highly susceptible to contract COVID19, and to develop a severe form. This has been confirmed in a first study in Spring, showing a mortality rate of 37%. Among all MM patients included in the cohort at the time of diagnosis of SARS-CoV-2 infection, blood samples will be collected at inclusion, at time of the infection acute phase in the most severe cases (when admitted in intensive care units), and at recovery. The following immune function tests will be evaluated, gammaglobulin measurements, lymphocytes counts, B, T, and NK cells analyses by cytometry, including exhaustion analyses. In addition, T cell repertoire sequencing looking for SARS-CoV-2- specific T cells, and serologies, will be evaluated at recovery and 6 months after MM treatment re-initiation.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
139
maximum 4 blood samples analyses per patient. At diagnosis of covid 19, in intensif care (if applicable), at covid19 recovery and 6 months after recovery
CHU Amiens SUD
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Angers, France
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Annecy, France
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Argenteuil, France
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Arras, France
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Auch, France
Characterize the immune laboratory parameters of Multiple Myeloma patients at the start of infection with COVID-19
gammaglobulin measurements in g/L
Time frame: up to one month following COVID-19 diagnosis
Characterize the immune laboratory parameters of Multiple Myeloma patients at the cure of COVID-19
gammaglobulin measurements in g/L
Time frame: one month following COVID-19 diagnosis
Characterize the immune laboratory parameters of Multiple Myeloma patients at the start of infection with COVID-19
lymphocytes counts in g/l
Time frame: up to one month following COVID-19 diagnosis
Characterize the immune laboratory parameters of Multiple Myeloma patients at the cure of COVID-19
lymphocytes counts in g/l
Time frame: one month following COVID-19 diagnosis
Characterize the immune laboratory parameters of Multiple Myeloma patients at the start of infection with COVID-19
number of cells B, T, and NK actived and inhibited
Time frame: up to one month following COVID-19 diagnosis
Characterize the immune laboratory parameters of Multiple Myeloma patientsat the cure of COVID-19
number of cells B, T, and NK actived and inhibited
Time frame: one month following COVID-19 diagnosis
Correlation of patient immune function with death or development of protective immunity
number of death
Time frame: up to 6 months following COVID-19 diagnosis
Number of patient with protective immune response
T cell repertoire sequencing looking for SARS-CoV-2- specific T cells, and serologies
Time frame: before the reintroduction of MM treatments, and 6 months later to evaluate if those treatments
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...and 43 more locations