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Applicability of probabilistic graphical models for early detection of SARS-CoV-2 reactive antibodies after SARS-CoV-2 vaccination in hematological patients.
Piñana, José Luis; Rodríguez-Belenguer, Pablo; Caballero, Dolores; Martino, Rodrigo; Lopez-Corral, Lucia; Terol, María-José; Vazquez, Lourdes; Calabuig, Marisa; Sanz-Linares, Gabriela; Marin-Jimenez, Francisca; Alonso, Carmen; Montoro, Juan; Ferrer, Elena; Facal, Ana; Pascual, María-Jesús; Rodriguez-Fernandez, Alicia; Olave, María T; Cascales-Hernandez, Almudena; Gago, Beatriz; Hernández-Rivas, José-Ángel; Villalon, Lucia; Corona, Magdalena; Roldán-Pérez, Alicia; Ribes-Amoros, Julia; González-Santillana, Clara; Garcia-Sanz, Ramon; Navarro, David; Serrano-López, Antonio J; Cedillo, Ángel; Soria-Olivas, Emilio; Sureda, Anna; Solano, Carlos.
  • Piñana JL; Hematology Department, Hospital Clínico Universitario de Valencia, Avda Blasco Ibañez, 17, 46010, Valencia, Spain. jlpinana@gmail.com.
  • Rodríguez-Belenguer P; Fundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain. jlpinana@gmail.com.
  • Caballero D; Research Program on Biomedical Informatics (GRIB), Department of Experimental and Health Sciences, Hospital del Mar Medical Research Institute (IMIM), Universitat Pompeu Fabra, Barcelona, Spain.
  • Martino R; Hematology department, University Hospital of Salamanca, IBSAL, CIBERONC, Centro de Investigación del Cáncer-IBMCC (USAL-CSIC), Salamanca, Spain.
  • Lopez-Corral L; Hematology Division, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
  • Terol MJ; Hematology department, University Hospital of Salamanca, IBSAL, CIBERONC, Centro de Investigación del Cáncer-IBMCC (USAL-CSIC), Salamanca, Spain.
  • Vazquez L; Hematology Department, Hospital Clínico Universitario de Valencia, Avda Blasco Ibañez, 17, 46010, Valencia, Spain.
  • Calabuig M; Fundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain.
  • Sanz-Linares G; Hematology department, University Hospital of Salamanca, IBSAL, CIBERONC, Centro de Investigación del Cáncer-IBMCC (USAL-CSIC), Salamanca, Spain.
  • Marin-Jimenez F; Hematology Department, Hospital Clínico Universitario de Valencia, Avda Blasco Ibañez, 17, 46010, Valencia, Spain.
  • Alonso C; Fundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain.
  • Montoro J; Clinical Hematology Division, Institut Català Oncologia-Hospitalet, IDIBELL, Universitat de Barcelona, Barcelona, Spain.
  • Ferrer E; Hematology Division, Hospital General universitari d'Elx, Elche, Spain.
  • Facal A; Hematology Division, Hospital Arnau de Vilanova, Valencia, Spain.
  • Pascual MJ; Hematology Division, Hospital universitario y politécnico La Fe, Valencia, Spain.
  • Rodriguez-Fernandez A; Hematology Department, Hospital Clínico Universitario de Valencia, Avda Blasco Ibañez, 17, 46010, Valencia, Spain.
  • Olave MT; Fundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain.
  • Cascales-Hernandez A; Hematology Division, Hospital universitario y politécnico La Fe, Valencia, Spain.
  • Gago B; Hematology Division, Hospital Regional Universitario Carlos Haya, Malaga, Spain.
  • Hernández-Rivas JÁ; Hematology Division, Hospital Universitario Virgen Macarena, Sevilla, Spain.
  • Villalon L; Hematology Division, Hospital Clínico Universitario Lozano Blesa, IIS Aragon, Zaragoza, Spain.
  • Corona M; Hematology Division, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain.
  • Roldán-Pérez A; Hematology Division, Hospital Regional Universitario Carlos Haya, Malaga, Spain.
  • Ribes-Amoros J; Hematology Division, Hospital Universitario Infanta Leonor, Madrid, Spain.
  • González-Santillana C; Hematology Division, Hospital Universitario Fundación Alcorcón, Madrid, Spain.
  • Garcia-Sanz R; Hematology Division, Hospital Ramon y Cajal, Madrid, Spain.
  • Navarro D; Hematology Division, Hospital Universitario Infanta Sofia, Madrid, Spain.
  • Serrano-López AJ; Clinical Hematology Division, Institut Català Oncologia-Hospitalet, IDIBELL, Universitat de Barcelona, Barcelona, Spain.
  • Cedillo Á; Hematology Division, Hospital Universitario de Fuenlabrada, Madrid, Spain.
  • Soria-Olivas E; Hematology department, University Hospital of Salamanca, IBSAL, CIBERONC, Centro de Investigación del Cáncer-IBMCC (USAL-CSIC), Salamanca, Spain.
  • Sureda A; Department of Medicine, School of Medicine, University of Valencia, Valencia, Spain.
  • Solano C; Microbiology department, Hospital Clinico Universitario de Valencia, Valencia, Spain.
Ann Hematol ; 101(9): 2053-2067, 2022 Sep.
Article in English | MEDLINE | ID: covidwho-1919767
ABSTRACT
Prior studies of antibody response after full SARS-CoV-2 vaccination in hematological patients have confirmed lower antibody levels compared to the general population. Serological response in hematological patients varies widely according to the disease type and its status, and the treatment given and its timing with respect to vaccination. Through probabilistic machine learning graphical models, we estimated the conditional probabilities of having detectable anti-SARS-CoV-2 antibodies at 3-6 weeks after SARS-CoV-2 vaccination in a large cohort of patients with several hematological diseases (n= 1166). Most patients received mRNA-based vaccines (97%), mainly Moderna® mRNA-1273 (74%) followed by Pfizer-BioNTech® BNT162b2 (23%). The overall antibody detection rate at 3 to 6 weeks after full vaccination for the entire cohort was 79%. Variables such as type of disease, timing of anti-CD20 monoclonal antibody therapy, age, corticosteroids therapy, vaccine type, disease status, or prior infection with SARS-CoV-2 are among the most relevant conditions influencing SARS-CoV-2-IgG-reactive antibody detection. A lower probability of having detectable antibodies was observed in patients with B-cell non-Hodgkin's lymphoma treated with anti-CD20 monoclonal antibodies within 6 months before vaccination (29.32%), whereas the highest probability was observed in younger patients with chronic myeloproliferative neoplasms (99.53%). The Moderna® mRNA-1273 compound provided higher probabilities of antibody detection in all scenarios. This study depicts conditional probabilities of having detectable antibodies in the whole cohort and in specific scenarios such as B cell NHL, CLL, MM, and cMPN that may impact humoral responses. These results could be useful to focus on additional preventive and/or monitoring interventions in these highly immunosuppressed hematological patients.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Antineoplastic Agents Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Ann Hematol Journal subject: Hematology Year: 2022 Document Type: Article Affiliation country: S00277-022-04906-8

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Antineoplastic Agents Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Ann Hematol Journal subject: Hematology Year: 2022 Document Type: Article Affiliation country: S00277-022-04906-8