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Does 18 F-FDG PET/CT add value to conventional imaging in clinical assessment of chronic disseminated candidiasis?
- Source :
-
Frontiers in medicine [Front Med (Lausanne)] 2022 Dec 20; Vol. 9, pp. 1026067. Date of Electronic Publication: 2022 Dec 20 (Print Publication: 2022). - Publication Year :
- 2022
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Abstract
- Background: Chronic disseminated candidiasis (CDC) classically occurs after profound and prolonged neutropenia. The aim of the CANHPARI study was to assess the clinical value of adding <superscript>18</superscript> F-fluorodeoxyglucose PET/CT to conventional radiology for initial and subsequent evaluations of CDC.<br />Materials and Methods: A pilot prospective study was conducted in 23 French onco-hematological centers from 2013 to 2017 (NCT01916057). Patients ≥ 18 y.o. suspected for CDC on abdominal conventional imaging (CT or MRI) were included. PET/CT and conventional imaging were performed at baseline and month 3 (M3). Follow-up was assessed until M12. The primary outcome measure was the global response at M3, i.e., apyrexia and complete response to PET/CT. The secondary outcome measure consists in comparison between responses to PET/CT and conventional imaging at diagnosis and M3.<br />Results: Among 52 included patients, 44 were evaluable (20 probable and 24 possible CDC); 86% had acute leukemia, 55% were male (median age 47 years). At diagnosis, 34% had fever and conventional imaging was always abnormal with microabscesses on liver and spleen in 66%, liver in 25%, spleen in 9%. Baseline PET/CT showed metabolic uptake on liver and/or spleen in 84% but did not match with lesion localizations on conventional imaging in 32%. M3 PET/CT showed no metabolic uptake in 13 (34%) patients, 11 still having pathological conventional imaging. Global response at M3 was observed in eight patients.<br />Conclusion: Baseline PET/CT does not replace conventional imaging for initial staging of CDC lesions but should be performed after 3 months of antifungal therapy.<br />Clinical Trial Registration: [www.clinicaltrials.gov], identifier [NCT01916057].<br />Competing Interests: BR has travel grants from Pfizer and MSD, speaker’s fees from MSD, Gilead, Astellas, and Iqone. SA has travel grants from MSD and Gilead, and speaker’s fee from Gilead. PiB has travel grants from Astellas, Pfizer, MSD, and Gilead, and speaker’s fee from MSD. OL speaker’s fees from MSD, Gilead, Astellas, Pfizer, and F2G, consultant Gilead. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2022 Rammaert, Maunoury, Rabeony, Correas, Elie, Alfandari, Berger, Rubio, Braun, Bakouboula, Candon, Montravers and Lortholary.)
Details
- Language :
- English
- ISSN :
- 2296-858X
- Volume :
- 9
- Database :
- MEDLINE
- Journal :
- Frontiers in medicine
- Publication Type :
- Academic Journal
- Accession number :
- 36606049
- Full Text :
- https://doi.org/10.3389/fmed.2022.1026067