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.