Organisational factors influencing early clinical trials enrollment: Gustave Roussy experience

Archive ouverte

Besle, Sylvain | Schultz, Emilien | Hollebecque, Antoine | Varga, Andreea | Baldini, Capucine | Martin, Patricia | Postel-Vinay, Sophie | Bahleda, Rastislav | Gazzah, Anas | Michot, Jean-Marie | Marabelle, Aurélien | Angevin, Eric | Armand, Jean-Pierre | Ribrag, Vincent | Soria, Jean-Charles | Massard, Christophe

Edité par CCSD ; Elsevier -

International audience. Abstract Anti-CD20 monoclonal antibodies are widely used for the treatment of hematological malignancies or autoimmune disease but may be responsible for a secondary humoral deficiency. In the context of COVID-19 infection, this may prevent the elicitation of a specific SARS-CoV-2 antibody response. We report a series of 17 consecutive patients with profound B-cell lymphopenia and prolonged COVID-19 symptoms, negative immunoglobulin G (IgG)-IgM SARS-CoV-2 serology, and positive RNAemia measured by digital polymerase chain reaction who were treated with 4 units of COVID-19 convalescent plasma. Within 48 hours of transfusion, all but 1 patient experienced an improvement of clinical symptoms. The inflammatory syndrome abated within a week. Only 1 patient who needed mechanical ventilation for severe COVID-19 disease died of bacterial pneumonia. SARS-CoV-2 RNAemia decreased to below the sensitivity threshold in all 9 evaluated patients. In 3 patients, virus-specific T-cell responses were analyzed using T-cell enzyme-linked immunospot assay before convalescent plasma transfusion. All showed a maintained SARS-CoV-2 T-cell response and poor cross-response to other coronaviruses. No adverse event was reported. Convalescent plasma with anti–SARS-CoV-2 antibodies appears to be a very promising approach in the context of protracted COVID-19 symptoms in patients unable to mount a specific humoral response to SARS-CoV-2.

Consulter en ligne

Suggestions

Du même auteur

Organisational factors influencing early clinical trials enrollment: Gustave Roussy experience

Archive ouverte | Besle, Sylvain | CCSD

International audience. PURPOSE:Enrolment process influences the likelihood of patients' inclusion in early clinical trials (ECT) through social, medical and organisational factors.PATIENTS AND METHODS:All patients ...

Safety, recommended dose, efficacy and immune correlates for nintedanib in combination with pembrolizumab in patients with advanced cancers

Archive ouverte | Baldini, Capucine | CCSD

International audience. Background: We aimed to determine the safety and efficacy of nintedanib, an oral anti-angiogenic tyrosine kinase inhibitor, in combination with pembrolizumab, an anti-PD1 immunotherapy, in pa...

Genome-driven medicine for patients with recurrent glioma enrolled in early phase trials

Archive ouverte | Baldini, Capucine | CCSD

International audience. Recent studies showed that patients with glioma can safely participate in early phase clinical trials; however, clinical benefits in this population were limited. We aimed to evaluate the ben...

Chargement des enrichissements...