<?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>2026-06-01T06:29:04Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/29770" metadataPrefix="marc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/29770</identifier><datestamp>2026-02-03T11:18:58Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37953</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">dc</subfield>
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      <subfield code="a">Jimeno, Antonio</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">García-Velasco, Adelaida</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">del Val, Olga</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">González-Billalabeitia, Enrique</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Hernando, Susana</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Hernández, Rosario</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Sánchez-Muñoz, Alfonso</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">López-Martın, Ana</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Durán, Ignacio</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Robles, Luis</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Corté-Funes, Hernán</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Paz-Ares, Luis</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="260">
      <subfield code="c">2004-03</subfield>
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      <subfield code="a">Cancer patients with fever and neutropenia currently are assessed&#xd;
on clinical grounds only. The current study prospectively evaluated the efficacy of&#xd;
baseline procalcitonin (PCT) in the detection of bacteremia and in the prediction&#xd;
of outcome in patients with solid tumors and febrile neutropenia.&#xd;
METHODS. PCT levels were determined at baseline and every 48 hours in 104&#xd;
patients undergoing chemotherapy who developed fever (axillary temperature&#xd;
  38 °C on 2 occasions or   38.3 °C in a single record) and neutropenia (absolute&#xd;
neutrophil count   500 cells/ L).&#xd;
RESULTS. The median baseline PCT values were significantly higher in patients&#xd;
who had microbiologically documented infections (1.24 ng/mL) compared with&#xd;
patients who had clinically documented infections (0.27 ng/mL) or fever of unknown&#xd;
origin (0.21 ng/mL; P   0.01). Accordingly, a PCT cut-off value of 0.5 ng/mL&#xd;
was reached more frequently in patients who had microbiologically documented&#xd;
infections compared with patients who had clinically documented infections or&#xd;
fever of unknown origin (66.7% vs. 13.4%, respectively; P   0.001). Furthermore,&#xd;
this threshold also was associated with an increased likelihood of treatment failure&#xd;
(70.0% vs. 14.9%; P   0.001). All 4 septic patients and all 5 patients who ultimately&#xd;
died presented PCT values 5-fold to 10-fold greater than the median values.&#xd;
Clinical evaluation in combination with baseline PCT assessment appeared to&#xd;
improve clinical risk evaluation alone.&#xd;
CONCLUSIONS. Baseline PCT levels were higher in patients who had febrile neutropenia&#xd;
with bacteremia compared with patients who had clinical infections or&#xd;
fever of unknown origin. PCT helped to identify patients who had microbiologic&#xd;
infections and patients who were at high risk of treatment failure, and PCT may&#xd;
constitute a complementary tool in the initial assessment of such patie</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">Jimeno A, García-Velasco A, del Val O, González-Billalabeitia E, Hernando S, Hernández R, Sánchez-Muñoz A, López-Martín A, Durán I, Robles L, Cortés-Funes H, Paz-Ares L. Assessment of procalcitonin as a diagnostic and prognostic marker in patients with solid tumors and febrile neutropenia. Cancer. 2004 Jun 1;100(11):2462-9. doi: 10.1002/cncr.20275. PMID: 15160353.</subfield>
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      <subfield code="a">https://hdl.handle.net/10630/29770</subfield>
   </datafield>
   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">10.1002/cncr.20275</subfield>
   </datafield>
   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">Cáncer - Diagnóstico</subfield>
   </datafield>
   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Assessment of Procalcitonin as a Diagnostic and Prognostic Marker in Patients with Solid Tumors and Febrile Neutropenia</subfield>
   </datafield>
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