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Antibody response after vaccination against SARS-CoV-2 in adults with hematological malignancies: a systematic review and meta-analysis.
Gagelmann, Nico; Passamonti, Francesco; Wolschke, Christine; Massoud, Radwan; Niederwieser, Christian; Adjallé, Raissa; Mora, Barbara; Ayuk, Francis; Kröger, Nicolaus.
  • Gagelmann N; Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg. n.gagelmann@uke.de.
  • Passamonti F; University of Insubria, Varese.
  • Wolschke C; Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg.
  • Massoud R; Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg.
  • Niederwieser C; Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg.
  • Adjallé R; Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg.
  • Mora B; University of Insubria, Varese.
  • Ayuk F; Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg.
  • Kröger N; Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg.
Haematologica ; 107(8): 1840-1849, 2022 08 01.
Article in English | MEDLINE | ID: covidwho-1974629
ABSTRACT
Vaccines against SARS-CoV-2 have shown remarkable efficacy and thus constitute an important preventive option against coronavirus disease 2019 (COVID-19), especially in fragile patients. We aimed to systematically analyze the outcomes of patients with hematological malignancies who received vaccination and to identify specific groups with differences in outcomes. The primary end point was antibody response after full vaccination (2 doses of mRNA or one dose of vectorbased vaccines). We identified 49 studies comprising 11,086 individuals. Overall risk of bias was low. The pooled response for hematological malignancies was 64% (95% confidence interval [CI] 59-69; I²=93%) versus 96% (95% CI 92-97; I²=44%) for solid cancer and 98% (95% CI 96-99; I²=55%) for healthy controls (P<0.001). Outcome was different across hematological malignancies (P<0.001). The pooled response was 50% (95% CI 43-57; I²=84%) for chronic lymphocytic leukemia, 76% (95% CI 67-83; I²=92%) for multiple myeloma, 83% (95% CI 69-91; I²=85%) for myeloproliferative neoplasms, 91% (95% CI 82-96; I²=12%) for Hodgkin lymphoma, and 58% (95% CI 44-70; I²=84%) for aggressive and 61% (95% CI 48-72; I²=85%) for indolent non-Hodgkin lymphoma. The pooled response for allogeneic and autologous hematopoietic cell transplantation was 82% and 83%, respectively. Being in remission and prior COVID-19 showed significantly higher responses. Low pooled response was identified for active treatment (35%), anti-CD20 therapy ≤1 year (15%), Bruton kinase inhibition (23%), venetoclax (26%), ruxolitinib (42%), and chimeric antigen receptor T-cell therapy (42%). Studies on timing, value of boosters, and long-term efficacy are needed. This study is registered with PROSPERO (clinicaltrials gov. Identifier CRD42021279051).
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Hematologic Neoplasms / COVID-19 Type of study: Experimental Studies / Prognostic study / Randomized controlled trials / Reviews / Systematic review/Meta Analysis Topics: Vaccines Limits: Adult / Humans Language: English Journal: Haematologica Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Hematologic Neoplasms / COVID-19 Type of study: Experimental Studies / Prognostic study / Randomized controlled trials / Reviews / Systematic review/Meta Analysis Topics: Vaccines Limits: Adult / Humans Language: English Journal: Haematologica Year: 2022 Document Type: Article