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CLL-461 Humoral Response to COVID-19 Vaccine: A Challenge in CLL
Chronic lymphocytic leukaemia (CLL) is associated with some degree of immune dysfunction as a result of the disease itself and/or treatment. COVID-19 has a major impact on patients with CLL who are at increased risk for severe disease and death. In this study, we aimed to understand the efficacy of...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9526679/ http://dx.doi.org/10.1016/S2152-2650(22)01348-9 |
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author | Capasso, Antonella Albi, Elisa Schiattone, Luana Martini, Francesca Sant'Antonio, Emanuela Scarfò, Lydia Ranghetti, Pamela Frenquelli, Michela Campanella, Alessandro Perotta, Eleonora Heltai, Silvia Colia, Maria Ghia, Paolo |
author_facet | Capasso, Antonella Albi, Elisa Schiattone, Luana Martini, Francesca Sant'Antonio, Emanuela Scarfò, Lydia Ranghetti, Pamela Frenquelli, Michela Campanella, Alessandro Perotta, Eleonora Heltai, Silvia Colia, Maria Ghia, Paolo |
author_sort | Capasso, Antonella |
collection | PubMed |
description | Chronic lymphocytic leukaemia (CLL) is associated with some degree of immune dysfunction as a result of the disease itself and/or treatment. COVID-19 has a major impact on patients with CLL who are at increased risk for severe disease and death. In this study, we aimed to understand the efficacy of anti-SARS-CoV-2 vaccines in patients with CLL. From January 2021, we collected data on 166 vaccinated patients with CLL followed at our site. Median age was 68 years (range 41-92); 43 (26%) were treatment-naïve (TN), 25 (15%) were previously treated, 95 (57%) were on active therapy, and 3 (2%) were experiencing relapse. Most patients received BNT162b2 (87%), followed by mRNA-1273 (4%) and ChAdOx1-S (3%); data is missing in 6%. Serology testing was performed with the SARS-CoV-2 S1/S2 IgG assay (Elecsys® Anti-SARS-CoV-2) 2 to 3 weeks after second and third vaccine doses and considered negative for antibody titers below 0.4 U/ml. Vaccine response was evaluated post-dose 2 in 119 patients and post-dose 3 in 74 patients. Post second dose, a higher seroconversion rate was observed in TN patients and those with sustained clinical response after therapy discontinuation (42% and 46% respectively) compared with actively treated patients (20.5%; [p=0.024; p=0.048]). Antibody response rate in patients receiving BTKi was considerably lower 19.7% (12/61). Three (42.9%) out of 7 patients who received venetoclax monotherapy seroconverted. None of the patients exposed to anti-CD20 antibodies (3/8 with targeted therapy, 2/8 with chemotherapy, 3/8 as single agent) <12 months before vaccination responded. Among patients actively treated who failed to achieve a humoral response after two-dose, 25.6% responded to the third dose of vaccine, although with a weak antibody level (median 8.64 U/ml, range 0.55-175). Overall, post third dose a higher median (IQR) antibody titer (127.9 U/mL; 0.55-2500) was observed compared to one post second dose (19.2 U/ml; 0.86-2500) in patients on therapy. Notably, all patients in clinical remission after treatment present titers above the upper limit of quantification (>2500 U/mL) post third dose. Conclusions: Humoral immune response to the COVID-19 vaccine is impaired in most patients with CLL and correlates with treatment status. |
format | Online Article Text |
id | pubmed-9526679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95266792022-10-03 CLL-461 Humoral Response to COVID-19 Vaccine: A Challenge in CLL Capasso, Antonella Albi, Elisa Schiattone, Luana Martini, Francesca Sant'Antonio, Emanuela Scarfò, Lydia Ranghetti, Pamela Frenquelli, Michela Campanella, Alessandro Perotta, Eleonora Heltai, Silvia Colia, Maria Ghia, Paolo Clin Lymphoma Myeloma Leuk Acute Lymphoblastic Leukemia Chronic lymphocytic leukaemia (CLL) is associated with some degree of immune dysfunction as a result of the disease itself and/or treatment. COVID-19 has a major impact on patients with CLL who are at increased risk for severe disease and death. In this study, we aimed to understand the efficacy of anti-SARS-CoV-2 vaccines in patients with CLL. From January 2021, we collected data on 166 vaccinated patients with CLL followed at our site. Median age was 68 years (range 41-92); 43 (26%) were treatment-naïve (TN), 25 (15%) were previously treated, 95 (57%) were on active therapy, and 3 (2%) were experiencing relapse. Most patients received BNT162b2 (87%), followed by mRNA-1273 (4%) and ChAdOx1-S (3%); data is missing in 6%. Serology testing was performed with the SARS-CoV-2 S1/S2 IgG assay (Elecsys® Anti-SARS-CoV-2) 2 to 3 weeks after second and third vaccine doses and considered negative for antibody titers below 0.4 U/ml. Vaccine response was evaluated post-dose 2 in 119 patients and post-dose 3 in 74 patients. Post second dose, a higher seroconversion rate was observed in TN patients and those with sustained clinical response after therapy discontinuation (42% and 46% respectively) compared with actively treated patients (20.5%; [p=0.024; p=0.048]). Antibody response rate in patients receiving BTKi was considerably lower 19.7% (12/61). Three (42.9%) out of 7 patients who received venetoclax monotherapy seroconverted. None of the patients exposed to anti-CD20 antibodies (3/8 with targeted therapy, 2/8 with chemotherapy, 3/8 as single agent) <12 months before vaccination responded. Among patients actively treated who failed to achieve a humoral response after two-dose, 25.6% responded to the third dose of vaccine, although with a weak antibody level (median 8.64 U/ml, range 0.55-175). Overall, post third dose a higher median (IQR) antibody titer (127.9 U/mL; 0.55-2500) was observed compared to one post second dose (19.2 U/ml; 0.86-2500) in patients on therapy. Notably, all patients in clinical remission after treatment present titers above the upper limit of quantification (>2500 U/mL) post third dose. Conclusions: Humoral immune response to the COVID-19 vaccine is impaired in most patients with CLL and correlates with treatment status. Elsevier Inc. 2022-10 2022-09-21 /pmc/articles/PMC9526679/ http://dx.doi.org/10.1016/S2152-2650(22)01348-9 Text en Copyright © 2022 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Acute Lymphoblastic Leukemia Capasso, Antonella Albi, Elisa Schiattone, Luana Martini, Francesca Sant'Antonio, Emanuela Scarfò, Lydia Ranghetti, Pamela Frenquelli, Michela Campanella, Alessandro Perotta, Eleonora Heltai, Silvia Colia, Maria Ghia, Paolo CLL-461 Humoral Response to COVID-19 Vaccine: A Challenge in CLL |
title | CLL-461 Humoral Response to COVID-19 Vaccine: A Challenge in CLL |
title_full | CLL-461 Humoral Response to COVID-19 Vaccine: A Challenge in CLL |
title_fullStr | CLL-461 Humoral Response to COVID-19 Vaccine: A Challenge in CLL |
title_full_unstemmed | CLL-461 Humoral Response to COVID-19 Vaccine: A Challenge in CLL |
title_short | CLL-461 Humoral Response to COVID-19 Vaccine: A Challenge in CLL |
title_sort | cll-461 humoral response to covid-19 vaccine: a challenge in cll |
topic | Acute Lymphoblastic Leukemia |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9526679/ http://dx.doi.org/10.1016/S2152-2650(22)01348-9 |
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