Publication:
Prevalence and clinical outcomes of carbapenemase-producing Enterobacterales (CPE) colonization in patients with solid organ malignancies: a prospective study

dc.contributor.coauthorArslan, Ş.
dc.contributor.coauthorBüyükkörük, M.
dc.contributor.coauthorErganiş, S.
dc.contributor.coauthorSoylu Koçoğlu, S.
dc.contributor.coauthorSavaş, G.
dc.contributor.coauthorÇağlar, K.
dc.contributor.coauthorÖzgen Top, Ö.
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorÖzger, Hasan Selçuk
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2026-09-15T10:54:20Z
dc.date.issued2026
dc.description.abstractTo 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.
dc.description.harvestedfromManual
dc.description.indexedbyPubMed
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipGazi University Scientific Research Projects (BAP) Unit (Grant: TGA-2024-9018)
dc.description.versionPublished Version
dc.identifier.doi10.1007/s10096-026-05638-7
dc.identifier.eissn1435-4373
dc.identifier.endpage-
dc.identifier.grantnoTGA-2024-9018
dc.identifier.issn0934-9723
dc.identifier.pubmed42711638
dc.identifier.startpage-
dc.identifier.urihttp://doi.org/10.1007/s10096-026-05638-7
dc.identifier.urihttps://hdl.handle.net/20.500.14288/35337
dc.languageeng
dc.publisherSpringer Science and Business Media LLC
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofEuropean Journal of Clinical Microbiology & Infectious Diseases
dc.relation.openaccessN/A
dc.subjectLife sciences
dc.subjectBiochemistry
dc.subjectGenetics and molecular biology
dc.subjectMolecular medicine
dc.subjectHealth sciences
dc.subjectMedicine
dc.subjectOncology
dc.subjectPharmacology
dc.titlePrevalence and clinical outcomes of carbapenemase-producing Enterobacterales (CPE) colonization in patients with solid organ malignancies: a prospective study
dc.typeJournal Article
dspace.entity.typePublication
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