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BNT162b2 mRNA COVID‐19 vaccine booster induces seroconversion in patients with B‐cell non‐Hodgkin lymphoma who failed to respond to two prior vaccine doses
Summary This prospective study evaluated seroconversion rates in response to BNT162b2 (Pfizer‐BioNTech) COVID‐19 vaccine booster in 44 B‐cell non‐Hodgkin lymphoma (B‐NHL) patients who failed to respond to two prior doses [42 previously exposed to anti‐CD20 monoclonal antibodies (moAbs) including 13...
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Published in: | British Journal of Haematology 2022-03, Vol.196 (6), p.1329-1333 |
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container_title | British Journal of Haematology |
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creator | Avivi, Irit Luttwak, Efrat Saiag, Esther Halperin, Tami Haberman, Shira Sarig, Ariel Levi, Sivan Aharon, Anat Herishanu, Yair Perry, Chava |
description | Summary
This prospective study evaluated seroconversion rates in response to BNT162b2 (Pfizer‐BioNTech) COVID‐19 vaccine booster in 44 B‐cell non‐Hodgkin lymphoma (B‐NHL) patients who failed to respond to two prior doses [42 previously exposed to anti‐CD20 monoclonal antibodies (moAbs) including 13 under maintenance treatment]. Seroconversion was obtained in 29.5% of the patients. Longer time from last anti‐CD20 moAb (>6 months) and diagnosis of aggressive lymphoma compared to other, incurable B‐NHLs were associated with increased seroconversion rates (47.8% vs.10.5%, p = 0.019 and 50% vs. 17.9%, p = 0.025 respectively). Thus, seronegative patients with B‐NHL that completed anti‐CD20 therapy more than 6 months prior to the booster have greater chances to achieve seroconversion. |
doi_str_mv | 10.1111/bjh.18029 |
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This prospective study evaluated seroconversion rates in response to BNT162b2 (Pfizer‐BioNTech) COVID‐19 vaccine booster in 44 B‐cell non‐Hodgkin lymphoma (B‐NHL) patients who failed to respond to two prior doses [42 previously exposed to anti‐CD20 monoclonal antibodies (moAbs) including 13 under maintenance treatment]. Seroconversion was obtained in 29.5% of the patients. Longer time from last anti‐CD20 moAb (>6 months) and diagnosis of aggressive lymphoma compared to other, incurable B‐NHLs were associated with increased seroconversion rates (47.8% vs.10.5%, p = 0.019 and 50% vs. 17.9%, p = 0.025 respectively). Thus, seronegative patients with B‐NHL that completed anti‐CD20 therapy more than 6 months prior to the booster have greater chances to achieve seroconversion.</description><identifier>ISSN: 0007-1048</identifier><identifier>EISSN: 1365-2141</identifier><identifier>DOI: 10.1111/bjh.18029</identifier><identifier>PMID: 35075635</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>BNT162 Vaccine ; BNT162b2 ; B‐cell non‐Hodgkin lymphoma ; CD20 antigen ; COVID-19 ; COVID-19 - prevention & control ; COVID-19 Vaccines ; COVID‐19 vaccine booster ; Hematology ; Humans ; humoral response ; Immunization, Secondary ; Lymphoma ; Lymphoma, Non-Hodgkin - therapy ; Monoclonal antibodies ; mRNA ; Non-Hodgkin's lymphoma ; Patients ; Prospective Studies ; RNA, Messenger ; SARS-CoV-2 ; Seroconversion ; Vaccines</subject><ispartof>British Journal of Haematology, 2022-03, Vol.196 (6), p.1329-1333</ispartof><rights>2022 British Society for Haematology and John Wiley & Sons Ltd.</rights><rights>2022. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the associated terms available at https://novel-coronavirus.onlinelibrary.wiley.com</rights><rights>2022 British Society for Haematology and John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4169-9398a2d6fc21bafa8910f1f3af05bb4f387bcb9ed315152972a75405d7e5e1413</citedby><cites>FETCH-LOGICAL-c4169-9398a2d6fc21bafa8910f1f3af05bb4f387bcb9ed315152972a75405d7e5e1413</cites><orcidid>0000-0002-7864-0089 ; 0000-0003-0212-2135</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2622736989?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,27922,27923,38514,43893</link.rule.ids><linktorsrc>$$Uhttps://www.proquest.com/docview/2622736989?pq-origsite=primo$$EView_record_in_ProQuest$$FView_record_in_$$GProQuest</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35075635$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Avivi, Irit</creatorcontrib><creatorcontrib>Luttwak, Efrat</creatorcontrib><creatorcontrib>Saiag, Esther</creatorcontrib><creatorcontrib>Halperin, Tami</creatorcontrib><creatorcontrib>Haberman, Shira</creatorcontrib><creatorcontrib>Sarig, Ariel</creatorcontrib><creatorcontrib>Levi, Sivan</creatorcontrib><creatorcontrib>Aharon, Anat</creatorcontrib><creatorcontrib>Herishanu, Yair</creatorcontrib><creatorcontrib>Perry, Chava</creatorcontrib><title>BNT162b2 mRNA COVID‐19 vaccine booster induces seroconversion in patients with B‐cell non‐Hodgkin lymphoma who failed to respond to two prior vaccine doses</title><title>British Journal of Haematology</title><addtitle>Br J Haematol</addtitle><description>Summary
This prospective study evaluated seroconversion rates in response to BNT162b2 (Pfizer‐BioNTech) COVID‐19 vaccine booster in 44 B‐cell non‐Hodgkin lymphoma (B‐NHL) patients who failed to respond to two prior doses [42 previously exposed to anti‐CD20 monoclonal antibodies (moAbs) including 13 under maintenance treatment]. Seroconversion was obtained in 29.5% of the patients. Longer time from last anti‐CD20 moAb (>6 months) and diagnosis of aggressive lymphoma compared to other, incurable B‐NHLs were associated with increased seroconversion rates (47.8% vs.10.5%, p = 0.019 and 50% vs. 17.9%, p = 0.025 respectively). Thus, seronegative patients with B‐NHL that completed anti‐CD20 therapy more than 6 months prior to the booster have greater chances to achieve seroconversion.</description><subject>BNT162 Vaccine</subject><subject>BNT162b2</subject><subject>B‐cell non‐Hodgkin lymphoma</subject><subject>CD20 antigen</subject><subject>COVID-19</subject><subject>COVID-19 - prevention & control</subject><subject>COVID-19 Vaccines</subject><subject>COVID‐19 vaccine booster</subject><subject>Hematology</subject><subject>Humans</subject><subject>humoral response</subject><subject>Immunization, Secondary</subject><subject>Lymphoma</subject><subject>Lymphoma, Non-Hodgkin - therapy</subject><subject>Monoclonal antibodies</subject><subject>mRNA</subject><subject>Non-Hodgkin's lymphoma</subject><subject>Patients</subject><subject>Prospective Studies</subject><subject>RNA, Messenger</subject><subject>SARS-CoV-2</subject><subject>Seroconversion</subject><subject>Vaccines</subject><issn>0007-1048</issn><issn>1365-2141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>COVID</sourceid><recordid>eNp9kc1u1DAUhS1ERaeFBS-ALLGhi7S-dpzEy87wM62qVkKFbWQ7NpMhsYOddDQ7HoFX4NV4krqdtgsk8OZeWZ_P9T0HoddAjiGdE7VeHUNFqHiGZsAKnlHI4TmaEULKDEhe7aODGNeEACMcXqB9xknJC8Zn6Pf88hoKqijuP1-e4sXV17P3f37-AoFvpNatM1h5H0cTcOuaSZuIowlee3djQmy9S9d4kGNr3Bjxph1XeJ6ea9N12HmX2qVvvn1PULfth5XvJd6sPLay7UyDR4-DiYN39-248XgIrQ9PoxsfTXyJ9qzsonn1UA_Rl48frhfL7OLq09ni9CLTORQiE0xUkjaF1RSUtLISQCxYJi3hSuWWVaXSSpiGAQdORUllyXPCm9Jwk-xih-jdTncI_sdk4lj3bbxbRDrjp1jTgtKCF7zkCX37F7r2U3Dpd4nKCaO8Avp_itKSFaISiTraUTr4GIOxdfKgl2FbA6nv0q1TuvV9uol986A4qd40T-RjnAk42QGb5O_230r1_Hy5k7wFuDuwEQ</recordid><startdate>202203</startdate><enddate>202203</enddate><creator>Avivi, Irit</creator><creator>Luttwak, Efrat</creator><creator>Saiag, Esther</creator><creator>Halperin, Tami</creator><creator>Haberman, Shira</creator><creator>Sarig, Ariel</creator><creator>Levi, Sivan</creator><creator>Aharon, Anat</creator><creator>Herishanu, Yair</creator><creator>Perry, Chava</creator><general>John Wiley & Sons, Inc</general><general>Blackwell Publishing Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>COVID</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7864-0089</orcidid><orcidid>https://orcid.org/0000-0003-0212-2135</orcidid></search><sort><creationdate>202203</creationdate><title>BNT162b2 mRNA COVID‐19 vaccine booster induces seroconversion in patients with B‐cell non‐Hodgkin lymphoma who failed to respond to two prior vaccine doses</title><author>Avivi, Irit ; Luttwak, Efrat ; Saiag, Esther ; Halperin, Tami ; Haberman, Shira ; Sarig, Ariel ; Levi, Sivan ; Aharon, Anat ; Herishanu, Yair ; Perry, Chava</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4169-9398a2d6fc21bafa8910f1f3af05bb4f387bcb9ed315152972a75405d7e5e1413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>BNT162 Vaccine</topic><topic>BNT162b2</topic><topic>B‐cell non‐Hodgkin lymphoma</topic><topic>CD20 antigen</topic><topic>COVID-19</topic><topic>COVID-19 - prevention & control</topic><topic>COVID-19 Vaccines</topic><topic>COVID‐19 vaccine booster</topic><topic>Hematology</topic><topic>Humans</topic><topic>humoral response</topic><topic>Immunization, Secondary</topic><topic>Lymphoma</topic><topic>Lymphoma, Non-Hodgkin - therapy</topic><topic>Monoclonal antibodies</topic><topic>mRNA</topic><topic>Non-Hodgkin's lymphoma</topic><topic>Patients</topic><topic>Prospective Studies</topic><topic>RNA, Messenger</topic><topic>SARS-CoV-2</topic><topic>Seroconversion</topic><topic>Vaccines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Avivi, Irit</creatorcontrib><creatorcontrib>Luttwak, Efrat</creatorcontrib><creatorcontrib>Saiag, Esther</creatorcontrib><creatorcontrib>Halperin, Tami</creatorcontrib><creatorcontrib>Haberman, Shira</creatorcontrib><creatorcontrib>Sarig, Ariel</creatorcontrib><creatorcontrib>Levi, Sivan</creatorcontrib><creatorcontrib>Aharon, Anat</creatorcontrib><creatorcontrib>Herishanu, Yair</creatorcontrib><creatorcontrib>Perry, Chava</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Coronavirus Research Database</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>British Journal of Haematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Avivi, Irit</au><au>Luttwak, Efrat</au><au>Saiag, Esther</au><au>Halperin, Tami</au><au>Haberman, Shira</au><au>Sarig, Ariel</au><au>Levi, Sivan</au><au>Aharon, Anat</au><au>Herishanu, Yair</au><au>Perry, Chava</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>BNT162b2 mRNA COVID‐19 vaccine booster induces seroconversion in patients with B‐cell non‐Hodgkin lymphoma who failed to respond to two prior vaccine doses</atitle><jtitle>British Journal of Haematology</jtitle><addtitle>Br J Haematol</addtitle><date>2022-03</date><risdate>2022</risdate><volume>196</volume><issue>6</issue><spage>1329</spage><epage>1333</epage><pages>1329-1333</pages><issn>0007-1048</issn><eissn>1365-2141</eissn><abstract>Summary
This prospective study evaluated seroconversion rates in response to BNT162b2 (Pfizer‐BioNTech) COVID‐19 vaccine booster in 44 B‐cell non‐Hodgkin lymphoma (B‐NHL) patients who failed to respond to two prior doses [42 previously exposed to anti‐CD20 monoclonal antibodies (moAbs) including 13 under maintenance treatment]. Seroconversion was obtained in 29.5% of the patients. Longer time from last anti‐CD20 moAb (>6 months) and diagnosis of aggressive lymphoma compared to other, incurable B‐NHLs were associated with increased seroconversion rates (47.8% vs.10.5%, p = 0.019 and 50% vs. 17.9%, p = 0.025 respectively). Thus, seronegative patients with B‐NHL that completed anti‐CD20 therapy more than 6 months prior to the booster have greater chances to achieve seroconversion.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>35075635</pmid><doi>10.1111/bjh.18029</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-7864-0089</orcidid><orcidid>https://orcid.org/0000-0003-0212-2135</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | BNT162 Vaccine BNT162b2 B‐cell non‐Hodgkin lymphoma CD20 antigen COVID-19 COVID-19 - prevention & control COVID-19 Vaccines COVID‐19 vaccine booster Hematology Humans humoral response Immunization, Secondary Lymphoma Lymphoma, Non-Hodgkin - therapy Monoclonal antibodies mRNA Non-Hodgkin's lymphoma Patients Prospective Studies RNA, Messenger SARS-CoV-2 Seroconversion Vaccines |
title | BNT162b2 mRNA COVID‐19 vaccine booster induces seroconversion in patients with B‐cell non‐Hodgkin lymphoma who failed to respond to two prior vaccine doses |
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