Abstract |
Studies that analyze the epidemiology and risk factors for invasive fungal disease (IFD) after engraftment in alloSCT are few in number. This single-center retrospective study included 404 alloSCT adult recipients surviving >40 days who engrafted and were discharged without prior IFD. All patients who received ⩾20 mg/day of prednisone were assigned to primary oral prophylaxis ( itraconazole or low-dose voriconazole). The primary end point was the cumulative incidence (CI) of probable/proven IFD using the European Organization for Research and Treatment of Cancer and Mycoses Study Group (EORTC/ MSG) criteria. The independent prognostic factors after multivariate analyses were used to construct a post-engraftment IFD risk score. The 1-year CI of IFD was 11%. The non-relapse mortality was 40% in those developing IFD and 16% in those who did not. The intent-to-treat analysis showed that 17% of patients abandoned the assigned prophylaxis. Age >40 years, ⩾1 previous SCT, pre-engraftment neutropenia >15 days, extensive chronic GVHD and CMV reactivation were independent risk factors. The post-engraftment IFD score stratified patients into low risk (0-1 factor, CI 0.7%), intermediate risk (2 factors, CI 9.9%) and high risk (3-5 factors, CI 24.7%) (P<0.0001). The antifungal prophylaxis strategy failed to prevent post-engraftment IFD in 11% of alloSCT. Our risk score could be useful to implement risk-adapted strategies using antifungal prophylaxis after engraftment.
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Authors | P Montesinos, R Rodríguez-Veiga, B Boluda, D Martínez-Cuadrón, I Cano, A Lancharro, J Sanz, M J Arilla, F López-Chuliá, I Navarro, I Lorenzo, M Salavert, J Pemán, P Calvillo, J Martínez, N Carpio, I Jarque, G F Sanz, M A Sanz |
Journal | Bone marrow transplantation
(Bone Marrow Transplant)
Vol. 50
Issue 11
Pg. 1465-72
(Nov 2015)
ISSN: 1476-5365 [Electronic] England |
PMID | 26281032
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antifungal Agents
- Echinocandins
- Lipopeptides
- Triazoles
- liposomal amphotericin B
- Granulocyte Colony-Stimulating Factor
- Amphotericin B
- Caspofungin
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Topics |
- Administration, Oral
- Adult
- Aged
- Allografts
- Amphotericin B
(therapeutic use)
- Antifungal Agents
(administration & dosage, therapeutic use)
- Aspergillosis
(drug therapy, epidemiology, etiology)
- Caspofungin
- Cause of Death
- Drug Therapy, Combination
- Echinocandins
(therapeutic use)
- Female
- Fungemia
(drug therapy, epidemiology, etiology)
- Granulocyte Colony-Stimulating Factor
(therapeutic use)
- Hematologic Neoplasms
(therapy)
- Hematopoietic Stem Cell Transplantation
- Humans
- Immunocompromised Host
- Incidence
- Lipopeptides
- Male
- Medication Adherence
- Middle Aged
- Mycoses
(drug therapy, epidemiology, etiology, prevention & control)
- Neutropenia
(prevention & control)
- Patient Compliance
- Premedication
- Retrospective Studies
- Risk Assessment
- Risk Factors
- Survival Analysis
- Transplantation Conditioning
(adverse effects)
- Treatment Failure
- Triazoles
(administration & dosage, therapeutic use)
- Young Adult
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