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Markers of neutrophil chemotaxis for identification of blood stream infections in children with acute lymphoblastic leukemia undergoing induction treatment.
Weischendorff, Sarah; De Pietri, Silvia; Rathe, Mathias; Frandsen, Thomas Leth; Hasle, Henrik; Nielsen, Claus H; Moser, Claus; Müller, Klaus.
Afiliação
  • Weischendorff S; Department of Pediatrics and Adolescent Medicine, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
  • De Pietri S; Institute for Inflammation Research, Center for Rheumatology and Spine Disease, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
  • Rathe M; Department of Pediatrics and Adolescent Medicine, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
  • Frandsen TL; Hans Christian Andersen Children's Hospital, Odense University Hospital, Odense, Denmark.
  • Hasle H; Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
  • Nielsen CH; Department of Pediatrics and Adolescent Medicine, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
  • Moser C; Department of Pediatrics, Aarhus University Hospital, Aarhus, Denmark.
  • Müller K; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Eur J Haematol ; 110(6): 762-771, 2023 Jun.
Article em En | MEDLINE | ID: mdl-36950865
ABSTRACT

BACKGROUND:

Although neutropenic fever is frequently observed during chemotherapy, only a minor proportion is caused by blood stream infections (BSI). This study investigated measurements of neutrophil chemotaxis as risk markers for BSI in children with acute lymphoblastic leukemia (ALL).

METHODS:

The chemokines CXCL1 and CXCL8 were measured weekly in 106 children with ALL during induction treatment. Information regarding BSI episodes was collected from the patients' medical records.

RESULTS:

During induction treatment, 102 (96%) patients developed profound neutropenia and 27 (25%) were diagnosed with BSI, debuting on median day 12 (range 4-29). Patients developing BSI had increased levels of CXCL1 on days 8 and 15 as well as increased CXCL8 on days 8, 15, 22, and 29 compared to patients without BSI (all p < 0.05). Patients with BSI < day 12 exhibited increased CXCL1 and CXCL8 levels as early as day 8 (81 vs. 4 pg/mL, p = 0.031 and 35 vs. 10 pg/mL, p < 0.0001, respectively), while CXCL1 and CXCL8 were increased on day 15 (215 vs. 57 pg/mL, p = 0.022 and 68 vs. 17 pg/mL, p = 0.0002) and after (all p < 0.01) in patients with BSI ≥ day 12.

CONCLUSION:

The markers of neutrophil chemotaxis, CXCL1, and CXCL8 may help to identify patients at increased risk of BSI during chemotherapy-induced neutropenia.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sepse / Leucemia-Linfoma Linfoblástico de Células Precursoras / Neutropenia Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Child / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sepse / Leucemia-Linfoma Linfoblástico de Células Precursoras / Neutropenia Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Child / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article