A 3-year study of Candida infections among patients with malignancy: etiologic agents and antifungal susceptibility profile

Front Cell Infect Microbiol. 2023 May 12:13:1152552. doi: 10.3389/fcimb.2023.1152552. eCollection 2023.

Abstract

Objective: Opportunistic fungal infections by Candida species arise among cancer patients due to the weakened immune system following extensive chemotherapy. Prophylaxis with antifungal agents have developed the resistance of Candida spp. to antifungals. Accurate identification of yeasts and susceptibility patterns are main concerns that can directly effect on the treatment of patients.

Methods: Over a period of three years, 325 cancer patients suspected to Candida infections were included in the current investigation. The clinical isolates were molecularly identified by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). All strains, were examined for in vitro susceptibility to the amphotericin B, itraconazole, fluconazole, and anidulafungin according to the CLSI M27 document.

Results: Seventy-four cancer patients had Candida infections (22.7%). Candida albicans was the most common species (83.8%). Antifungal susceptibility results indicated that 100% of the Candida isolates were sensitive to amphotericin B; however, 17.6%, 9.4%, and 5.4% of clinical isolates were resistant to anidulafungin, fluconazole, and itraconazole, respectively.

Conclusion: The findings of the present work shows a warning increase in resistance to echinocandins. Since all fluconazole resistance isolates were obtained from candidemia, we recommend amphotericin B as the first line therapy for this potentially fatal infection.

Keywords: Candida infections; antifungal susceptibility; epidemiology; malignancy; molecular identification.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amphotericin B / pharmacology
  • Amphotericin B / therapeutic use
  • Anidulafungin / therapeutic use
  • Antifungal Agents / pharmacology
  • Antifungal Agents / therapeutic use
  • Candida
  • Candidemia* / drug therapy
  • Candidemia* / microbiology
  • Candidiasis* / microbiology
  • Drug Resistance, Fungal
  • Fluconazole / pharmacology
  • Fluconazole / therapeutic use
  • Humans
  • Itraconazole / therapeutic use
  • Microbial Sensitivity Tests
  • Neoplasms* / complications

Substances

  • Antifungal Agents
  • Fluconazole
  • Amphotericin B
  • Itraconazole
  • Anidulafungin

Grants and funding

The Project was financially supported by a grant from the Isfahan University of Medical Sciences (no. 399985).