Gastrointestinal barrier integrity and mucosal inflammation as risk factors of blood stream infections in children treated for acute lymphoblastic leukaemia

Author:

De Pietri Silvia1ORCID,Weischendorff Sarah12ORCID,Rathe Mathias34,Frandsen Thomas Leth1,Hasle Henrik56,Nersting Jacob1,Nielsen Claus H.2,Moser Claus7,Müller Klaus128

Affiliation:

1. Department of Paediatrics and Adolescent Medicine Rigshospitalet, Copenhagen University Hospital Copenhagen Denmark

2. Institute for Inflammation Research, Center for Rheumatology and Spine Disease Rigshospitalet, Copenhagen University Hospital Copenhagen Denmark

3. Hans Christian Andersen Children's Hospital Odense University Hospital Odense Denmark

4. Department of Clinical Research University of Southern Denmark Odense Denmark

5. Department of Paediatrics Aarhus University Hospital Aarhus Denmark

6. Department of Clinical Medicine Aarhus University Aarhus Denmark

7. Department of Clinical Microbiology Rigshospitalet, Copenhagen University Hospital Copenhagen Denmark

8. Institute of Clinical Medicine University of Copenhagen Copenhagen Denmark

Abstract

AbstractChemotherapy‐induced mucositis increases the risk of blood stream infections (BSI) due to translocation of bacteria across the intestinal epithelium. Our study investigated if quantitative measures of intestinal mucositis severity, including plasma citrulline (a marker of functional enterocytes) and CCL20 (an intestinal immune homeostatic chemokine), could identify patients at risk of BSI. A total of 106 children with ALL undergoing induction treatment (NOPHO ALL 2008) were included and information regarding BSI episodes was collected from the patients' medical records. Twenty‐seven patients (25%) developed BSI during induction. Patients with BSI had a larger decrease in citrulline after chemotherapy than patients without BSI, and nearly all BSI episodes (25/27) occurred in the group of patients exhibiting a drop in citrulline (OR = 6.4 [95% CI: 1.4‐29.3], P = .008). Patients who developed BSI had higher plasma CCL20 levels on days 8, 15 and 22 than patients without BSI (all P < .05), and elevated CCL20 levels on day 8 increased the risk of subsequent BSI (OR = 1.57 [1.11‐2.22] per doubling of CCL20 level, P = .01) in a multivariable logistic regression analysis. These findings suggest that children with ALL who develop BSI during chemotherapy are characterised by more severe intestinal mucositis, as measured by plasma citrulline and CCL20. These markers may be useful in early risk stratification to guide treatment decisions.

Publisher

Wiley

Subject

Cancer Research,Oncology

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