<?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>2026-05-17T01:16:07Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/11344" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/11344</identifier><datestamp>2024-11-29T23:20:21Z</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">Cedena, Maria-Teresa</subfield>
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      <subfield code="a">Martin-Clavero, Estela</subfield>
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      <subfield code="a">Wong, Sandy</subfield>
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      <subfield code="a">Shah, Nina</subfield>
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      <subfield code="a">Bahri, Natasha</subfield>
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      <subfield code="a">Alonso, Rafael</subfield>
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      <subfield code="a">Barcenas, Carmen</subfield>
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      <subfield code="a">Valeri, Antonio</subfield>
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      <subfield code="a">Salazar Tabares, Johny</subfield>
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      <subfield code="a">Sanchez-Pina, Jose</subfield>
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      <subfield code="a">Cuellar, Clara</subfield>
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      <subfield code="a">Martin, Thomas</subfield>
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      <subfield code="a">Wolf, Jeffrey</subfield>
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      <subfield code="a">Lahuerta, Juan José</subfield>
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      <subfield code="a">Martinez-Lopez, Joaquin</subfield>
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      <subfield code="c">2020-08-31</subfield>
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      <subfield code="a">Stringent complete response (sCR) is used as a deeper response category than complete response (CR) in multiple myeloma (MM) but may be of limited value in the era of minimal residual disease (MRD) testing.&#xd;
Here, we used 4-colour multiparametric flow cytometry (MFC) or next-generation sequencing (NGS) of immunoglobulin genes to analyse and compare the prognostic impact of sCR and MRD monitoring. We included 193 treated patients in two institutions achieving CR, for which both bone marrow aspirates and biopsies were available.&#xd;
We found that neither the serum free light chain ratio, clonality by immunohistochemistry (IHC) nor plasma cell bone marrow infiltration identified CR patients at distinct risk. Patients with sCR had slightly longer progression-free survival. Nevertheless, persistent clonal bone marrow disease was detectable using MFC or NGS and was associated with significantly inferior outcomes compared with MRD-negative cases.&#xd;
Our results confirm that sCR does not predict a different outcome and indicate that more sensitive techniques are able to identify patients with differing prognoses. We suggest that MRD categories should be implemented over sCR for the future classification of MM responses.</subfield>
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      <subfield code="a">PLoS One  2020 ;15(8):e0237155.</subfield>
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      <subfield code="a">10.1371/journal.pone.0237155</subfield>
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      <subfield code="a">PloS one</subfield>
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      <subfield code="a">32866200</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/11344</subfield>
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      <subfield code="a">STEM-CELL TRANSPLANTATION</subfield>
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      <subfield code="a">DEEP-SEQUENCING METHOD</subfield>
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      <subfield code="a">CRITERIA</subfield>
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      <subfield code="a">THERAPY</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">The clinical significance of stringent complete response in multiple myeloma is surpassed by minimal residual disease measurements.</subfield>
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