The outcomes for 73
invasive fusariosis patients treated with
voriconazole were investigated. Patients with proven (n = 67) or probable (n = 6)
infections were identified from the
voriconazole clinical database (n = 39) and the French National Reference Center for
Mycoses and Antifungals database (n = 34). Investigator-determined success was a complete or partial response. Survival was determined from day 1 of
voriconazole therapy to the last day known alive. Patients were 2 to 79 years old (median, 43 years), and 66% were male. Identified Fusarium species (62%) were F. solani, F. moniliforme, F. proliferatum, and F. oxysporum. Underlying conditions analyzed included hematopoietic stem cell transplant (HSCT; 18%),
hematologic malignancy (HM; 60%), chronic immunosuppression (CI; 12%), or other condition (OC; 10%).
Infection sites were brain (5%), disseminated excluding brain (67%), lungs/sinus (15%), and other (12%). Most patients (64%) were or had recently been neutropenic (<500 cells/mm(3)).
Therapy duration was 1 to 480 days (median, 57 days), with a 47% success rate. Baseline
neutropenia impacted success adversely (P ≤ 0.03). Success varied by underlying condition (HSCT, 38%; HM, 45%; CI, 44%; OC, 71%) and
infection site (brain, 0%; disseminated, 45%; other, 56%; lung/sinus, 64%) (P > 0.05). Combination
therapy (13 patients) was no better than treatment with
voriconazole alone. Overall, 59% of the patients died (49% died of
fusariosis), and 90-day survival was 42%. Site of
infection influenced survival (P = 0.02). Median survival (in days) by species was as follows: F. solani, 213; F. oxysporum, 112; Fusarium spp., 101; F. proliferatum, 84; F. moniliforme, 76. We conclude that
voriconazole is a therapeutic option for
invasive fusariosis.