TABLE 1.
Possible role and indications for echinocandins in the treatment of invasive aspergillosis
Indication | Aima | Situation | Level of evidence (Ref.) |
---|---|---|---|
First-line treatment (monotherapy) | To treat IA when no alternative regimen (or potential risks outweighing benefits for other regimens) | Relative contraindications to azoles (underlying liver disease, drug-drug interactions, prolonged QT interval); relative contraindications to AMB (underlying kidney disease, nephrotoxic comedications) | Noncomparative prospective or retrospective studies (overall success rate, 30–90%) (62) |
Second-line treatment (monotherapy) | To treat IA when first-line antifungals have failed or need to be discontinued | Toxicity of triazoles (hepatic test disturbances, visual/neurological side effects); toxicity of AMB (acute renal failure); failure of previous antifungal regimens | Noncomparative prospective or retrospective studies (overall success rate, 30–70%) (62) |
In combination with triazoles or AMB | To obtain synergistic interactions (triazoles, AMB) | Severe and/or disseminated IA, galactomannan-positive IA; in case of failure of previous regimen or breakthrough IA; for IA due to azole-resistant A. fumigatus | One randomized controlled trial (trends, benefit limited to subgroup analyses) (81); expert opinion; murine models (75, 77) |
To palliate potential PK/PD defect until first-line drug achieves appropriate serum level (triazoles) | In severe and/or disseminated IA | Expert opinion | |
To palliate potential inefficacy of first-line drug (triazoles) | For empirical treatment, if suspicion or high local prevalence of azole-resistant A. fumigatus; breakthrough IA | Expert opinion (82) | |
To obtain synergistic interactions on biofilms (triazoles, AMB) | For Aspergillus endocarditis or osteomyelitis with presence of prosthetic material | In vitro studies (79) |
AMB, amphotericin B; IA, invasive aspergillosis; PK/PD, pharmacokinetic/pharmacodynamic.