Publication: Prevalence and clinical outcomes of carbapenemase-producing Enterobacterales (CPE) colonization in patients with solid organ malignancies: a prospective study
Program
KU-Authors
KU Authors
Co-Authors
Arslan, Ş.
Büyükkörük, M.
Erganiş, S.
Soylu Koçoğlu, S.
Savaş, G.
Çağlar, K.
Özgen Top, Ö.
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Compiler & Affiliation
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Date
Language
eng
Type
Embargo Status
Journal Title
Journal ISSN
Volume Title
Alternative Title
Abstract
To evaluate the prevalence of carbapenemase-producing Enterobacterales (CPE) colonization in patients with solid organ malignancies and investigate its association with severe infection, infection free survival, and mortality through prospective follow-up. METHODS: This single-center, prospective, observational study (July 2024-July 2025) included adult patients with lung, genitourinary, or gastrointestinal cancers at Gazi University Hospital. Rectal swabs were screened using chromogenic agar, and isolates were identified by MALDI-TOF MS. Meropenem susceptibility was determined via disk diffusion. Carbapenemase genes (OXA-48, NDM, KPC, VIM, IMP) were detected using an in-house multiplex PCR. All patients were followed for six months. RESULTS: Among 269 patients, the CPE colonization prevalence was 9.7% (n=26). E. coli and K. pneumoniae were the predominant isolates (46.2% each), with OXA-48 being the most frequent gene (84.6%), followed by NDM (11.5%). No significant differences were found between CPE-colonized and non-colonized patients regarding severe infection rates (34.6% vs 35.8%, p=0.904), infection-free survival (p=0.314), or mortality at 30, 90, and 180 days (p=0.481, p=0.519, and p=0.239). Among colonized patients, the rectal colonizing strain was phenotypically concordant with the causative pathogen of subsequent severe infection in 15.4% (n=4) of the cases. The median time to infection was 12 days (IQR, 6-15 days). CONCLUSIONS: Gastrointestinal CPE colonization in patients with solid organ malignancies was primarily driven by OXA-48-producing E. coli and K. pneumoniae. Although colonization did not significantly increase the overall risk of severe infection or mortality in this cohort, further large-scale, multicenter studies are needed to identify specific high-risk subgroups.
Source
Publisher
Springer Science and Business Media LLC
Subject
Life sciences, Biochemistry, Genetics and molecular biology, Molecular medicine, Health sciences, Medicine, Oncology, Pharmacology
Citation
Has Part
Source
European Journal of Clinical Microbiology & Infectious Diseases
Book Series Title
Edition
DOI
10.1007/s10096-026-05638-7
