Cargando…

2334. The effectiveness of bivalent COVID-19 booster among patients with hematologic malignancies

BACKGROUND: Patients with hematologic malignancies remain at higher risk for developing severe SARS-CoV-2 infections and have reduced immune responses to vaccines. METHODS: A prospective observational study was conducted at Brigham and Women’s Hospital and Dana-Farber Cancer Institute from January 2...

Descripción completa

Detalles Bibliográficos
Autores principales: Aleissa, Muneerah M, Davey, Sonya, Rooks, Rebecca, Izaguirre, Natalie E, Yates, Bridget, Kanwal, Urwah, Baden, Lindsey R, Issa, Nicolas C, Sherman, Amy C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677953/
http://dx.doi.org/10.1093/ofid/ofad500.1956
_version_ 1785150251267522560
author Aleissa, Muneerah M
Davey, Sonya
Rooks, Rebecca
Izaguirre, Natalie E
Yates, Bridget
Kanwal, Urwah
Baden, Lindsey R
Issa, Nicolas C
Sherman, Amy C
author_facet Aleissa, Muneerah M
Davey, Sonya
Rooks, Rebecca
Izaguirre, Natalie E
Yates, Bridget
Kanwal, Urwah
Baden, Lindsey R
Issa, Nicolas C
Sherman, Amy C
author_sort Aleissa, Muneerah M
collection PubMed
description BACKGROUND: Patients with hematologic malignancies remain at higher risk for developing severe SARS-CoV-2 infections and have reduced immune responses to vaccines. METHODS: A prospective observational study was conducted at Brigham and Women’s Hospital and Dana-Farber Cancer Institute from January 2021 to May 2023. Adult participants were included if they had a history of lymphoid malignancy (LM) or had received hematopoietic stem cell transplantation (HSCT). SARS-CoV-2 antibodies were measured before vaccination and every 2-3 months thereafter. COVID-19 vaccination history and SARS-CoV-2 infections (by report or positive PCR) were recorded longitudinally. Our primary outcome for this study was to evaluate the incidence of breakthrough SARS-CoV-2 infections after receiving a bivalent COVID-19 vaccine booster (Omicron/wildtype). RESULTS: A total of 144 participants were included in the analysis. Of those, 98 (68%) received a bivalent COVID-19 booster. The median age was 68 (IQR 61 – 73) and 51 (52%) were male. The majority of participants 61 (62%) had LM and 37 (38%) underwent HSCT with a median time from transplant to first vaccine of 317 days (IQR 171 – 742). Overall, the incidence of breakthrough SARS-CoV-2 infections was 13 (13%) (Figure) with a median time from vaccination to breakthrough infection of 72 days (IQR 54 – 112). There were no SARS-CoV-2 related mortality or severe disease leading to hospitalization in our cohort. Figure [Figure: see text] CONCLUSION: Our analysis demonstrates a low incidence of breakthrough SARS-CoV-2 infections and no severe disease among those who received a bivalent mRNA vaccine, highlighting the potential protection of the bivalent booster against SARS-CoV-2 in patients with hematologic malignancies who had previously been vaccinated or boosted. Further studies are warranted to determine the optimal number and type of booster vaccinations needed to protect this vulnerable population. DISCLOSURES: Nicolas C. Issa, MD, AiCuris: Grant/Research Support|Astellas: Grant/Research Support|Boehringer Ingelheim: Advisor/Consultant|Fujifilm: Grant/Research Support|GSK: Grant/Research Support|Merck: Grant/Research Support|Moderna: Grant/Research Support
format Online
Article
Text
id pubmed-10677953
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-106779532023-11-27 2334. The effectiveness of bivalent COVID-19 booster among patients with hematologic malignancies Aleissa, Muneerah M Davey, Sonya Rooks, Rebecca Izaguirre, Natalie E Yates, Bridget Kanwal, Urwah Baden, Lindsey R Issa, Nicolas C Sherman, Amy C Open Forum Infect Dis Abstract BACKGROUND: Patients with hematologic malignancies remain at higher risk for developing severe SARS-CoV-2 infections and have reduced immune responses to vaccines. METHODS: A prospective observational study was conducted at Brigham and Women’s Hospital and Dana-Farber Cancer Institute from January 2021 to May 2023. Adult participants were included if they had a history of lymphoid malignancy (LM) or had received hematopoietic stem cell transplantation (HSCT). SARS-CoV-2 antibodies were measured before vaccination and every 2-3 months thereafter. COVID-19 vaccination history and SARS-CoV-2 infections (by report or positive PCR) were recorded longitudinally. Our primary outcome for this study was to evaluate the incidence of breakthrough SARS-CoV-2 infections after receiving a bivalent COVID-19 vaccine booster (Omicron/wildtype). RESULTS: A total of 144 participants were included in the analysis. Of those, 98 (68%) received a bivalent COVID-19 booster. The median age was 68 (IQR 61 – 73) and 51 (52%) were male. The majority of participants 61 (62%) had LM and 37 (38%) underwent HSCT with a median time from transplant to first vaccine of 317 days (IQR 171 – 742). Overall, the incidence of breakthrough SARS-CoV-2 infections was 13 (13%) (Figure) with a median time from vaccination to breakthrough infection of 72 days (IQR 54 – 112). There were no SARS-CoV-2 related mortality or severe disease leading to hospitalization in our cohort. Figure [Figure: see text] CONCLUSION: Our analysis demonstrates a low incidence of breakthrough SARS-CoV-2 infections and no severe disease among those who received a bivalent mRNA vaccine, highlighting the potential protection of the bivalent booster against SARS-CoV-2 in patients with hematologic malignancies who had previously been vaccinated or boosted. Further studies are warranted to determine the optimal number and type of booster vaccinations needed to protect this vulnerable population. DISCLOSURES: Nicolas C. Issa, MD, AiCuris: Grant/Research Support|Astellas: Grant/Research Support|Boehringer Ingelheim: Advisor/Consultant|Fujifilm: Grant/Research Support|GSK: Grant/Research Support|Merck: Grant/Research Support|Moderna: Grant/Research Support Oxford University Press 2023-11-27 /pmc/articles/PMC10677953/ http://dx.doi.org/10.1093/ofid/ofad500.1956 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Aleissa, Muneerah M
Davey, Sonya
Rooks, Rebecca
Izaguirre, Natalie E
Yates, Bridget
Kanwal, Urwah
Baden, Lindsey R
Issa, Nicolas C
Sherman, Amy C
2334. The effectiveness of bivalent COVID-19 booster among patients with hematologic malignancies
title 2334. The effectiveness of bivalent COVID-19 booster among patients with hematologic malignancies
title_full 2334. The effectiveness of bivalent COVID-19 booster among patients with hematologic malignancies
title_fullStr 2334. The effectiveness of bivalent COVID-19 booster among patients with hematologic malignancies
title_full_unstemmed 2334. The effectiveness of bivalent COVID-19 booster among patients with hematologic malignancies
title_short 2334. The effectiveness of bivalent COVID-19 booster among patients with hematologic malignancies
title_sort 2334. the effectiveness of bivalent covid-19 booster among patients with hematologic malignancies
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677953/
http://dx.doi.org/10.1093/ofid/ofad500.1956
work_keys_str_mv AT aleissamuneerahm 2334theeffectivenessofbivalentcovid19boosteramongpatientswithhematologicmalignancies
AT daveysonya 2334theeffectivenessofbivalentcovid19boosteramongpatientswithhematologicmalignancies
AT rooksrebecca 2334theeffectivenessofbivalentcovid19boosteramongpatientswithhematologicmalignancies
AT izaguirrenataliee 2334theeffectivenessofbivalentcovid19boosteramongpatientswithhematologicmalignancies
AT yatesbridget 2334theeffectivenessofbivalentcovid19boosteramongpatientswithhematologicmalignancies
AT kanwalurwah 2334theeffectivenessofbivalentcovid19boosteramongpatientswithhematologicmalignancies
AT badenlindseyr 2334theeffectivenessofbivalentcovid19boosteramongpatientswithhematologicmalignancies
AT issanicolasc 2334theeffectivenessofbivalentcovid19boosteramongpatientswithhematologicmalignancies
AT shermanamyc 2334theeffectivenessofbivalentcovid19boosteramongpatientswithhematologicmalignancies