<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-27T03:43:12Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/16139" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/16139</identifier><datestamp>2024-11-29T14:21:30Z</datestamp><setSpec>com_20.500.12105_2173</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_19597</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Miyaoka, Masashi</subfield>
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      <subfield code="a">Kikuti, Yara Yukie</subfield>
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      <subfield code="a">Carreras, Joaquim</subfield>
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      <subfield code="a">Ito, Atsushi</subfield>
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      <subfield code="a">Ikoma, Haruka</subfield>
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      <subfield code="a">Tomita, Sakura</subfield>
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      <subfield code="a">Kawada, Hiroshi</subfield>
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      <subfield code="a">Roncador, Giovanna</subfield>
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      <subfield code="a">Bea, Silvia</subfield>
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      <subfield code="a">Campo, Elias</subfield>
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      <subfield code="a">Nakamura, Naoya</subfield>
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      <subfield code="c">2022-11-27</subfield>
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      <subfield code="a">Diffuse large B-cell lymphoma (DLBCL) with MYC alteration is classified as high-grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements (double/triple-hit lymphoma; DHL/THL), DLBCL with MYC rearrangement (single-hit lymphoma; SHL) and DLBCL with MYC-cluster amplification (MCAD). To elucidate the genetic features of DHL/THL, SHL, and MCAD, 23 lymphoma cases from Tokai University Hospital were analyzed. The series included 10 cases of DHL/THL, 10 cases of SHL and 3 cases of MCAD. The analysis used whole-genome copy number microarray analysis (OncoScan) and a custom-made next-generation sequencing (NGS) panel of 115 genes associated with aggressive B-cell lymphomas. The copy number alteration (CNA) profiles were similar between DHL/THL and SHL. MCAD had fewer CNAs than those of DHL/THL and SHL, except for +8q24. The NGS profile characterized DHL/THL with a higher "mutation burden" than SHL (17 vs. 10, p = 0.010), and the most relevant genes for DHL/THL were BCL2 and SOCS1, and for SHL was DTX1. MCAD was characterized by mutations of DDX3X, TCF3, HLA-A, and TP53, whereas MYC was unmutated. In conclusion, DHL/THL, SHL, and MCAD have different profiles.</subfield>
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      <subfield code="a">Cancers (Basel). 2022 ;14(23):5849.</subfield>
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      <subfield code="a">Cancers</subfield>
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      <subfield code="a">SURVIVAL</subfield>
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      <subfield code="a">DLBCL</subfield>
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      <subfield code="a">DDX3X</subfield>
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      <subfield code="a">Copy Number Alteration and Mutational Profile of High-Grade B-Cell Lymphoma with MYC and BCL2 and/or BCL6 Rearrangements, Diffuse Large B-Cell Lymphoma with MYC-Rearrangement, and Diffuse Large B-Cell Lymphoma with MYC-Cluster Amplification.</subfield>
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