6533b7d0fe1ef96bd125adf9
RESEARCH PRODUCT
SARS-CoV-2 vaccine response and rate of breakthrough infection in patients with hematological disorders
José Luis PiñanaLucia López-corralRodrigo MartinoLourdes VázquezAriafna PérezGabriel Andrés Martin-martinBeatriz GagoGabriela Sanz-linaresAndrés Sanchez-salinasLucia VillalonVenancio ConesaMaria T. OlaveMagdalena CoronaSara Marcos CorralesMar Tormo DiazJose ÁNgel Hernández-rivasJuan MontoroAlicia Rodriguez-fernandezIrene Risco GálvezPablo Rodríguez-belenguerJuan Carlos Hernandez-boludaIrene García-cadenasMontserrat Ruiz-garcíaJuan Luis Muñoz-bellidoCarlos Solano VercetÁNgel CedilloAnna SuredaDavid Navarro OrtegaInfectious Complications Subcommittee Of The Spanish Hematopoietic Stem Cell Transplantationsubject
*Pfizer-BioNTech BNT162b2Cancer ResearchCOVID-19 Vaccines*Hematological malignanciesAutologous stem cell transplantationAntibodies ViralBreakthrough SARS-CoV-2 infectionModerna mRNA-1273Cohort StudiesHematological malignancies*Moderna mRNA-1273Correlates of protection*VaccineHumansProspective StudiesVacunacióPfizer-BioNTech BNT162b2Molecular BiologyBNT162 Vaccine*Immunocompromised patients*Correlates of protectionSARS-CoV-2VaccinationHematologic diseasesCOVID-19Hematology*Breakthrough SARS-CoV-2 infectionHematologic DiseasesSARS-CoV-2 vaccinesAllogeneic stem cell transplantationVirusOncologyMalalties hematològiquesImmunocompromised patients*SARS-CoV-2 vaccines*Autologous stem cell transplantation*COVID-19Vaccine*Allogeneic stem cell transplantationdescription
Abstract Background The clinical efficacy of SARS-CoV-2 vaccines according to antibody response in immunosuppressed patients such as hematological patients has not yet been established. Patients and methods A prospective multicenter registry-based cohort study conducted from December 2020 to December 2021 by the Spanish transplant and cell therapy group was used to analyze the relationship of antibody response at 3–6 weeks after full vaccination (2 doses) with breakthrough SARS-CoV-2 infection in 1394 patients with hematological disorders. Results At a median follow-up of 165 days after complete immunization, 37 out of 1394 (2.6%) developed breakthrough SARS-CoV-2 infection at median of 77 days (range 7–195) after full vaccination. The incidence rate was 6.39 per 100 persons-year. Most patients were asymptomatic (19/37, 51.4%), whereas only 19% developed pneumonia. The mortality rate was 8%. Lack of detectable antibodies at 3–6 weeks after full vaccination was the only variable associated with breakthrough infection in multivariate logistic regression analysis (Odds Ratio 2.35, 95% confidence interval 1.2–4.6, p = 0.012). Median antibody titers were lower in cases than in non-cases [1.83 binding antibody units (BAU)/mL (range 0–4854.93) vs 730.81 BAU/mL (range 0–56,800), respectively (p = 0.007)]. We identified 250 BAU/mL as a cutoff above which incidence and severity of the infection were significantly lower. Conclusions Our study highlights the benefit of developing an antibody response in these highly immunosuppressed patients. Level of antibody titers at 3 to 6 weeks after 2-dose vaccination links with protection against both breakthrough infection and severe disease for non-Omicron SARS-CoV-2 variants.
year | journal | country | edition | language |
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2022-05-07 | Journal of Hematology & Oncology |