Cargando…

The serological prevalence of SARS‐CoV‐2 infection in patients with chronic myeloid leukemia is similar to that in the general population

BACKGROUND: Patients with hematological malignancies are at an increased risk of SARS‐CoV‐2 disease (COVID‐19) and adverse outcome. However, a low mortality rate has been reported in patients with chronic myeloid leukemia (CML). Preclinical evidence suggests that tyrosine kinase inhibitors (TKIs) ma...

Descripción completa

Detalles Bibliográficos
Autores principales: Bonifacio, Massimiliano, Tiribelli, Mario, Miggiano, Maria Cristina, Abruzzese, Elisabetta, Binotto, Gianni, Scaffidi, Luigi, Cordioli, Maddalena, Damiani, Daniela, Di Bona, Eros, Trawinska, Malgorzata Monika, Tanasi, Ilaria, Dubbini, Maria Vittoria, Velotta, Vanessa, Ceccarelli, Giulia, Pierdomenico, Elisabetta, Lo Schirico, Mariella, Semenzato, Gianpietro, Ruggeri, Marco, Fanin, Renato, Tacconelli, Evelina, Pizzolo, Giovanni, Krampera, Mauro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446554/
https://www.ncbi.nlm.nih.gov/pubmed/34464516
http://dx.doi.org/10.1002/cam4.4179
_version_ 1784568905443835904
author Bonifacio, Massimiliano
Tiribelli, Mario
Miggiano, Maria Cristina
Abruzzese, Elisabetta
Binotto, Gianni
Scaffidi, Luigi
Cordioli, Maddalena
Damiani, Daniela
Di Bona, Eros
Trawinska, Malgorzata Monika
Tanasi, Ilaria
Dubbini, Maria Vittoria
Velotta, Vanessa
Ceccarelli, Giulia
Pierdomenico, Elisabetta
Lo Schirico, Mariella
Semenzato, Gianpietro
Ruggeri, Marco
Fanin, Renato
Tacconelli, Evelina
Pizzolo, Giovanni
Krampera, Mauro
author_facet Bonifacio, Massimiliano
Tiribelli, Mario
Miggiano, Maria Cristina
Abruzzese, Elisabetta
Binotto, Gianni
Scaffidi, Luigi
Cordioli, Maddalena
Damiani, Daniela
Di Bona, Eros
Trawinska, Malgorzata Monika
Tanasi, Ilaria
Dubbini, Maria Vittoria
Velotta, Vanessa
Ceccarelli, Giulia
Pierdomenico, Elisabetta
Lo Schirico, Mariella
Semenzato, Gianpietro
Ruggeri, Marco
Fanin, Renato
Tacconelli, Evelina
Pizzolo, Giovanni
Krampera, Mauro
author_sort Bonifacio, Massimiliano
collection PubMed
description BACKGROUND: Patients with hematological malignancies are at an increased risk of SARS‐CoV‐2 disease (COVID‐19) and adverse outcome. However, a low mortality rate has been reported in patients with chronic myeloid leukemia (CML). Preclinical evidence suggests that tyrosine kinase inhibitors (TKIs) may have a protective role against severe COVID‐19. METHODS: We conducted a cross‐sectional study of 564 consecutive patients with CML who were tested for anti‐SARS‐CoV‐2 IgG/IgM antibodies at their first outpatient visit between May and early November 2020 in five hematologic centers representative of three Italian regions. RESULTS: The estimated serological prevalence of SARS‐CoV‐2 infection in patients with CML after the first pandemic wave was similar to that in the general population (about 2%), both at national and regional levels. CML patients with positive anti‐SARS‐CoV‐2 serology were more frequently male (p = 0.027) and active workers (p = 0.012), while there was no significant association with TKI treatment type. Only 3 out of 11 IgG‐positive patients had previously received a molecular diagnosis of COVID‐19, while the remainders were asymptomatic or with mild symptoms. CONCLUSIONS: Our data confirm that the course of SARS‐CoV‐2 infection in patients with CML is generally mild and reassure about the safety of continuing TKIs during the COVID‐19 pandemic. Furthermore, we suggest that patients with CML succeed to mount an antibody response after exposure to SARS‐CoV‐2, similar to the general population.
format Online
Article
Text
id pubmed-8446554
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-84465542021-09-22 The serological prevalence of SARS‐CoV‐2 infection in patients with chronic myeloid leukemia is similar to that in the general population Bonifacio, Massimiliano Tiribelli, Mario Miggiano, Maria Cristina Abruzzese, Elisabetta Binotto, Gianni Scaffidi, Luigi Cordioli, Maddalena Damiani, Daniela Di Bona, Eros Trawinska, Malgorzata Monika Tanasi, Ilaria Dubbini, Maria Vittoria Velotta, Vanessa Ceccarelli, Giulia Pierdomenico, Elisabetta Lo Schirico, Mariella Semenzato, Gianpietro Ruggeri, Marco Fanin, Renato Tacconelli, Evelina Pizzolo, Giovanni Krampera, Mauro Cancer Med Clinical Cancer Research BACKGROUND: Patients with hematological malignancies are at an increased risk of SARS‐CoV‐2 disease (COVID‐19) and adverse outcome. However, a low mortality rate has been reported in patients with chronic myeloid leukemia (CML). Preclinical evidence suggests that tyrosine kinase inhibitors (TKIs) may have a protective role against severe COVID‐19. METHODS: We conducted a cross‐sectional study of 564 consecutive patients with CML who were tested for anti‐SARS‐CoV‐2 IgG/IgM antibodies at their first outpatient visit between May and early November 2020 in five hematologic centers representative of three Italian regions. RESULTS: The estimated serological prevalence of SARS‐CoV‐2 infection in patients with CML after the first pandemic wave was similar to that in the general population (about 2%), both at national and regional levels. CML patients with positive anti‐SARS‐CoV‐2 serology were more frequently male (p = 0.027) and active workers (p = 0.012), while there was no significant association with TKI treatment type. Only 3 out of 11 IgG‐positive patients had previously received a molecular diagnosis of COVID‐19, while the remainders were asymptomatic or with mild symptoms. CONCLUSIONS: Our data confirm that the course of SARS‐CoV‐2 infection in patients with CML is generally mild and reassure about the safety of continuing TKIs during the COVID‐19 pandemic. Furthermore, we suggest that patients with CML succeed to mount an antibody response after exposure to SARS‐CoV‐2, similar to the general population. John Wiley and Sons Inc. 2021-08-31 /pmc/articles/PMC8446554/ /pubmed/34464516 http://dx.doi.org/10.1002/cam4.4179 Text en © 2021 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Bonifacio, Massimiliano
Tiribelli, Mario
Miggiano, Maria Cristina
Abruzzese, Elisabetta
Binotto, Gianni
Scaffidi, Luigi
Cordioli, Maddalena
Damiani, Daniela
Di Bona, Eros
Trawinska, Malgorzata Monika
Tanasi, Ilaria
Dubbini, Maria Vittoria
Velotta, Vanessa
Ceccarelli, Giulia
Pierdomenico, Elisabetta
Lo Schirico, Mariella
Semenzato, Gianpietro
Ruggeri, Marco
Fanin, Renato
Tacconelli, Evelina
Pizzolo, Giovanni
Krampera, Mauro
The serological prevalence of SARS‐CoV‐2 infection in patients with chronic myeloid leukemia is similar to that in the general population
title The serological prevalence of SARS‐CoV‐2 infection in patients with chronic myeloid leukemia is similar to that in the general population
title_full The serological prevalence of SARS‐CoV‐2 infection in patients with chronic myeloid leukemia is similar to that in the general population
title_fullStr The serological prevalence of SARS‐CoV‐2 infection in patients with chronic myeloid leukemia is similar to that in the general population
title_full_unstemmed The serological prevalence of SARS‐CoV‐2 infection in patients with chronic myeloid leukemia is similar to that in the general population
title_short The serological prevalence of SARS‐CoV‐2 infection in patients with chronic myeloid leukemia is similar to that in the general population
title_sort serological prevalence of sars‐cov‐2 infection in patients with chronic myeloid leukemia is similar to that in the general population
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446554/
https://www.ncbi.nlm.nih.gov/pubmed/34464516
http://dx.doi.org/10.1002/cam4.4179
work_keys_str_mv AT bonifaciomassimiliano theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT tiribellimario theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT miggianomariacristina theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT abruzzeseelisabetta theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT binottogianni theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT scaffidiluigi theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT cordiolimaddalena theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT damianidaniela theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT dibonaeros theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT trawinskamalgorzatamonika theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT tanasiilaria theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT dubbinimariavittoria theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT velottavanessa theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT ceccarelligiulia theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT pierdomenicoelisabetta theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT loschiricomariella theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT semenzatogianpietro theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT ruggerimarco theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT faninrenato theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT tacconellievelina theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT pizzologiovanni theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT kramperamauro theserologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT bonifaciomassimiliano serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT tiribellimario serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT miggianomariacristina serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT abruzzeseelisabetta serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT binottogianni serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT scaffidiluigi serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT cordiolimaddalena serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT damianidaniela serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT dibonaeros serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT trawinskamalgorzatamonika serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT tanasiilaria serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT dubbinimariavittoria serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT velottavanessa serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT ceccarelligiulia serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT pierdomenicoelisabetta serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT loschiricomariella serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT semenzatogianpietro serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT ruggerimarco serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT faninrenato serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT tacconellievelina serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT pizzologiovanni serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation
AT kramperamauro serologicalprevalenceofsarscov2infectioninpatientswithchronicmyeloidleukemiaissimilartothatinthegeneralpopulation