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Published on: July 1, 2020
Breakthrough candidemia with hematological disease: Results from a single-center retrospective study in Japan,
Ruriko Nishida1, Yoshihiro Eriguchi1, Noriko Miyake1
1Department of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Science, Fukuoka, Japan.
Insights
Breakthrough candidemia in hematologic patients is often caused by Candida guilliermondii complex and Candida parapsilosis, which show reduced echinocandin susceptibility. Hematopoietic stem cell transplant patients face higher mortality rates from this infection.
Area of Science:
- Medical Mycology
- Infectious Diseases
- Hematology
Background:
- Breakthrough candidemia (BrC) poses a significant threat to immunocompromised individuals, especially those with hematological disorders.
- Echinocandin antifungal agents are frequently used in treating BrC, but emerging resistance is a concern.
Purpose of the Study:
- To characterize BrC in hematologic patients treated with novel antifungal agents.
- To investigate the impact of antifungal resistance and patient characteristics on outcomes.
Main Methods:
- Retrospective analysis of 40 BrC cases in patients with hematologic disease from 2009-2020.
- Clinical and microbiological data collection, including antifungal susceptibility testing and genetic analysis (FKS polymorphisms).
Main Results:
- Candida guilliermondii complex (32.5%) and Candida parapsilosis (30%) were the most common isolates.
- These species exhibited reduced echinocandin susceptibility due to FKS gene polymorphisms, despite in vitro susceptibility.
- Patients receiving hematopoietic stem cell transplant (HSCT)-related therapy had a significantly higher 30-day mortality rate (55.2%) compared to those not receiving it (18.2%).
- C. guilliermondii complex BrC in HSCT patients treated with echinocandins had a high mortality rate (53.8%) and risk of persistent infection.
Conclusions:
- Candida guilliermondii complex breakthrough candidemia is a potentially fatal condition in HSCT patients, particularly when treated with echinocandins.
- The prevalence of echinocandin-reduced-susceptible strains like C. guilliermondii complex may be linked to widespread echinocandin use.
- Further research into optimal treatment strategies for resistant candidemia in immunocompromised patients is warranted.
Abstract:
Breakthrough candidemia (BrC) is a significant problem in immunocompromised patients, particularly those with hematological disorders. To assess the characteristics of BrC in patients with hematologic disease treated with novel antifungal agents, we collected clinical and microbiological information on said patients from 2009 to 2020 in our institution. Forty cases were identified, of which 29 (72.5%) received hematopoietic stem cell transplant (HSCT)-related therapy. At BrC onset, the most administered class of antifungal agents were echinocandins, administered to 70% of patients. Candida guilliermondii complex was the most frequently isolated species (32.5%), followed by C. parapsilosis (30%). These two isolates were echinocandin-susceptible in vitro but had naturally occurring FKS gene polymorphisms that reduced echinocandin susceptibility. Frequent isolation of these echinocandin-reduced-susceptible strains in BrC may be associated with the widespread use of echinocandins. In this study, the 30-day crude mortality rate in the group receiving HSCT-related therapy was significantly higher than in the group not receiving it (55.2% versus 18.2%, P = .0297). Most patients affected by C. guilliermondii complex BrC (92.3%) received HSCT-related therapy and had a 30-day mortality rate of 53.8%; despite treatment administration, 3 of 13 patients had persistent candidemia. Based on our results, C. guilliermondii complex BrC is a potentially fatal condition in patients receiving HSCT-related therapy with echinocandin administration.
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