Benign and malignant hematologic manifestations in patients with VEXAS syndrome due to somatic mutations in UBA1
Somatic mutations in UBA1 involving hematopoietic stem and myeloid cells have been reported in patients with the newly defined VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome. Here, we report clinical hematologic manifestations and unique bone marrow (BM) features in 16 pat...
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creator | Obiorah, Ifeyinwa Emmanuela Patel, Bhavisha A. Groarke, Emma M. Wang, Weixin Trick, Megan Ombrello, Amanda K. Ferrada, Marcela A. Wu, Zhijie Gutierrez-Rodrigues, Fernanda Lotter, Jennifer Wilson, Lorena Hoffmann, Patrycja Cardona, Daniela Ospina Patel, Nisha Dulau-Florea, Alina Kastner, Daniel L. Grayson, Peter C. Beck, David B. Young, Neal S. Calvo, Katherine R. |
description | Somatic mutations in UBA1 involving hematopoietic stem and myeloid cells have been reported in patients with the newly defined VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome. Here, we report clinical hematologic manifestations and unique bone marrow (BM) features in 16 patients with VEXAS. All patients were male and had a history of severe autoinflammatory and rheumatologic manifestations and a somatic UBA1 mutation (p.Met41). Ten patients had hematologic disorders: myelodysplastic syndrome (MDS; 6 of 16), multiple myeloma (2 of 16), monoclonal gammopathy of undetermined significance (2 of 16), and monoclonal B-cell lymphocytosis (2 of 16), and a few of those patients had 2 co-existing clonal processes. Although macrocytic anemia (100%) and lymphopenia (80%) were prevalent in all patients with VEXAS, thrombocytopenia and neutropenia were more common in patients with progression to MDS. All BMs in VEXAS patients had prominent cytoplasmic vacuoles in myeloid and erythroid precursors. In addition, most BMs were hypercellular with myeloid hyperplasia, erythroid hypoplasia, and varying degrees of dysplasia. All patients diagnosed with MDS were lower risk (low blast count, very good to intermediate cytogenetics) according to standard prognostic scoring with no known progression to leukemia. In addition, 10 of 16 patients had thrombotic events, including venous thromboembolism and arterial stroke. Although VEXAS presents symptomatically as a rheumatologic disease, morbidity and mortality are associated with progression to hematologic disease. Given the increased risk of developing MDS and multiple myeloma, surveillance for disease progression is important.
•Patients with VEXAS syndrome have a propensity toward developing cytopenia, MDS, multiple myeloma, and venous thromboembolism.•BM from patients with VEXAS shows characteristic vacuolization of myeloid and erythroid precursors.
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doi_str_mv | 10.1182/bloodadvances.2021004976 |
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•Patients with VEXAS syndrome have a propensity toward developing cytopenia, MDS, multiple myeloma, and venous thromboembolism.•BM from patients with VEXAS shows characteristic vacuolization of myeloid and erythroid precursors.
[Display omitted]</description><identifier>ISSN: 2473-9529</identifier><identifier>EISSN: 2473-9537</identifier><identifier>DOI: 10.1182/bloodadvances.2021004976</identifier><identifier>PMID: 34427584</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Bone Marrow ; Humans ; Male ; Monoclonal Gammopathy of Undetermined Significance ; Multiple Myeloma ; Mutation ; Myelodysplastic Syndromes ; Myeloid Neoplasia</subject><ispartof>Blood advances, 2021-08, Vol.5 (16), p.3203-3215</ispartof><rights>2021 American Society of Hematology</rights><rights>2021 by The American Society of Hematology.</rights><rights>2021 by The American Society of Hematology 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c479t-6d61aeb6eff4f0fc35e267fa1319cd3f7ac5cc695f418aa8d345b2429449d8153</citedby><cites>FETCH-LOGICAL-c479t-6d61aeb6eff4f0fc35e267fa1319cd3f7ac5cc695f418aa8d345b2429449d8153</cites><orcidid>0000-0003-3984-0819 ; 0000-0001-6285-7382 ; 0000-0002-0771-4191 ; 0000-0003-3116-4588 ; 0000-0002-4648-5926</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8405186/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8405186/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34427584$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Obiorah, Ifeyinwa Emmanuela</creatorcontrib><creatorcontrib>Patel, Bhavisha A.</creatorcontrib><creatorcontrib>Groarke, Emma M.</creatorcontrib><creatorcontrib>Wang, Weixin</creatorcontrib><creatorcontrib>Trick, Megan</creatorcontrib><creatorcontrib>Ombrello, Amanda K.</creatorcontrib><creatorcontrib>Ferrada, Marcela A.</creatorcontrib><creatorcontrib>Wu, Zhijie</creatorcontrib><creatorcontrib>Gutierrez-Rodrigues, Fernanda</creatorcontrib><creatorcontrib>Lotter, Jennifer</creatorcontrib><creatorcontrib>Wilson, Lorena</creatorcontrib><creatorcontrib>Hoffmann, Patrycja</creatorcontrib><creatorcontrib>Cardona, Daniela Ospina</creatorcontrib><creatorcontrib>Patel, Nisha</creatorcontrib><creatorcontrib>Dulau-Florea, Alina</creatorcontrib><creatorcontrib>Kastner, Daniel L.</creatorcontrib><creatorcontrib>Grayson, Peter C.</creatorcontrib><creatorcontrib>Beck, David B.</creatorcontrib><creatorcontrib>Young, Neal S.</creatorcontrib><creatorcontrib>Calvo, Katherine R.</creatorcontrib><title>Benign and malignant hematologic manifestations in patients with VEXAS syndrome due to somatic mutations in UBA1</title><title>Blood advances</title><addtitle>Blood Adv</addtitle><description>Somatic mutations in UBA1 involving hematopoietic stem and myeloid cells have been reported in patients with the newly defined VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome. Here, we report clinical hematologic manifestations and unique bone marrow (BM) features in 16 patients with VEXAS. All patients were male and had a history of severe autoinflammatory and rheumatologic manifestations and a somatic UBA1 mutation (p.Met41). Ten patients had hematologic disorders: myelodysplastic syndrome (MDS; 6 of 16), multiple myeloma (2 of 16), monoclonal gammopathy of undetermined significance (2 of 16), and monoclonal B-cell lymphocytosis (2 of 16), and a few of those patients had 2 co-existing clonal processes. Although macrocytic anemia (100%) and lymphopenia (80%) were prevalent in all patients with VEXAS, thrombocytopenia and neutropenia were more common in patients with progression to MDS. All BMs in VEXAS patients had prominent cytoplasmic vacuoles in myeloid and erythroid precursors. In addition, most BMs were hypercellular with myeloid hyperplasia, erythroid hypoplasia, and varying degrees of dysplasia. All patients diagnosed with MDS were lower risk (low blast count, very good to intermediate cytogenetics) according to standard prognostic scoring with no known progression to leukemia. In addition, 10 of 16 patients had thrombotic events, including venous thromboembolism and arterial stroke. Although VEXAS presents symptomatically as a rheumatologic disease, morbidity and mortality are associated with progression to hematologic disease. Given the increased risk of developing MDS and multiple myeloma, surveillance for disease progression is important.
•Patients with VEXAS syndrome have a propensity toward developing cytopenia, MDS, multiple myeloma, and venous thromboembolism.•BM from patients with VEXAS shows characteristic vacuolization of myeloid and erythroid precursors.
[Display omitted]</description><subject>Bone Marrow</subject><subject>Humans</subject><subject>Male</subject><subject>Monoclonal Gammopathy of Undetermined Significance</subject><subject>Multiple Myeloma</subject><subject>Mutation</subject><subject>Myelodysplastic Syndromes</subject><subject>Myeloid Neoplasia</subject><issn>2473-9529</issn><issn>2473-9537</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUU1vEzEUtBCIVqV_AfnIJcXfXl-QkqrQSpU4QBE3y7GfE6NdO6x3U_Xf4yoltCdOHvnNzHuaQQhTckFpxz6u-1KCC3uXPdQLRhglRBitXqFTJjRfGMn16yNm5gSd1_qLEEK14tKwt-iEC8G07MQp2q0gp03GLgc8uL5Blye8hcFNpS-b5NtvThHq5KZUcsUp412DkKeK79O0xT-ufi6_4fqQw1gGwGEGPBVcS3N4VM_PhHerJX2H3kTXVzh_es_Q3eer75fXi9uvX24ul7cLL7SZFioo6mCtIEYRSfRcAlM6Osqp8YFH7bz0XhkZBe2c6wIXcs0EM0KY0FHJz9Cng-9uXg8QfDt4dL3djWlw44MtLtmXk5y2dlP2thNE0k41gw9PBmP5PbcA7JCqh753GcpcLZNKUN4ZTRu1O1D9WGodIR7XUGIfO7MvOrP_OmvS98_PPAr_NtQIqwMBWlj7BKOtvqXvIaQR_GRDSf_f8gccw7B_</recordid><startdate>20210824</startdate><enddate>20210824</enddate><creator>Obiorah, Ifeyinwa Emmanuela</creator><creator>Patel, Bhavisha A.</creator><creator>Groarke, Emma M.</creator><creator>Wang, Weixin</creator><creator>Trick, Megan</creator><creator>Ombrello, Amanda K.</creator><creator>Ferrada, Marcela A.</creator><creator>Wu, Zhijie</creator><creator>Gutierrez-Rodrigues, Fernanda</creator><creator>Lotter, Jennifer</creator><creator>Wilson, Lorena</creator><creator>Hoffmann, Patrycja</creator><creator>Cardona, Daniela Ospina</creator><creator>Patel, Nisha</creator><creator>Dulau-Florea, Alina</creator><creator>Kastner, Daniel L.</creator><creator>Grayson, Peter C.</creator><creator>Beck, David B.</creator><creator>Young, Neal S.</creator><creator>Calvo, Katherine R.</creator><general>Elsevier Inc</general><general>American Society of Hematology</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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-3984-0819</orcidid><orcidid>https://orcid.org/0000-0001-6285-7382</orcidid><orcidid>https://orcid.org/0000-0002-0771-4191</orcidid><orcidid>https://orcid.org/0000-0003-3116-4588</orcidid><orcidid>https://orcid.org/0000-0002-4648-5926</orcidid></search><sort><creationdate>20210824</creationdate><title>Benign and malignant hematologic manifestations in patients with VEXAS syndrome due to somatic mutations in UBA1</title><author>Obiorah, Ifeyinwa Emmanuela ; 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Here, we report clinical hematologic manifestations and unique bone marrow (BM) features in 16 patients with VEXAS. All patients were male and had a history of severe autoinflammatory and rheumatologic manifestations and a somatic UBA1 mutation (p.Met41). Ten patients had hematologic disorders: myelodysplastic syndrome (MDS; 6 of 16), multiple myeloma (2 of 16), monoclonal gammopathy of undetermined significance (2 of 16), and monoclonal B-cell lymphocytosis (2 of 16), and a few of those patients had 2 co-existing clonal processes. Although macrocytic anemia (100%) and lymphopenia (80%) were prevalent in all patients with VEXAS, thrombocytopenia and neutropenia were more common in patients with progression to MDS. All BMs in VEXAS patients had prominent cytoplasmic vacuoles in myeloid and erythroid precursors. In addition, most BMs were hypercellular with myeloid hyperplasia, erythroid hypoplasia, and varying degrees of dysplasia. All patients diagnosed with MDS were lower risk (low blast count, very good to intermediate cytogenetics) according to standard prognostic scoring with no known progression to leukemia. In addition, 10 of 16 patients had thrombotic events, including venous thromboembolism and arterial stroke. Although VEXAS presents symptomatically as a rheumatologic disease, morbidity and mortality are associated with progression to hematologic disease. Given the increased risk of developing MDS and multiple myeloma, surveillance for disease progression is important.
•Patients with VEXAS syndrome have a propensity toward developing cytopenia, MDS, multiple myeloma, and venous thromboembolism.•BM from patients with VEXAS shows characteristic vacuolization of myeloid and erythroid precursors.
[Display omitted]</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>34427584</pmid><doi>10.1182/bloodadvances.2021004976</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0003-3984-0819</orcidid><orcidid>https://orcid.org/0000-0001-6285-7382</orcidid><orcidid>https://orcid.org/0000-0002-0771-4191</orcidid><orcidid>https://orcid.org/0000-0003-3116-4588</orcidid><orcidid>https://orcid.org/0000-0002-4648-5926</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Bone Marrow Humans Male Monoclonal Gammopathy of Undetermined Significance Multiple Myeloma Mutation Myelodysplastic Syndromes Myeloid Neoplasia |
title | Benign and malignant hematologic manifestations in patients with VEXAS syndrome due to somatic mutations in UBA1 |
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