Effect of Caspofungin vs Fluconazole Prophylaxis on Invasive Fungal Disease Among Children and Young Adults With Acute Myeloid Leukemia: A Randomized Clinical Trial.


Journal

JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160

Informations de publication

Date de publication:
05 11 2019
Historique:
entrez: 6 11 2019
pubmed: 7 11 2019
medline: 23 11 2019
Statut: ppublish

Résumé

Children, adolescents, and young adults with acute myeloid leukemia are at high risk of life-threatening invasive fungal disease with both yeasts and molds. To compare the efficacy of caspofungin vs fluconazole prophylaxis against proven or probable invasive fungal disease and invasive aspergillosis during neutropenia following acute myeloid leukemia chemotherapy. This multicenter, randomized, open-label, clinical trial enrolled patients aged 3 months to 30 years with newly diagnosed de novo, relapsed, or secondary acute myeloid leukemia being treated at 115 US and Canadian institutions (April 2011-November 2016; last follow-up June 30, 2018). Participants were randomly assigned during the first chemotherapy cycle to prophylaxis with caspofungin (n = 257) or fluconazole (n = 260). Prophylaxis was administered during the neutropenic period following each chemotherapy cycle. The primary outcome was proven or probable invasive fungal disease as adjudicated by blinded central review. Secondary outcomes were invasive aspergillosis, empirical antifungal therapy, and overall survival. The second interim efficacy analysis and an unplanned futility analysis based on 394 patients appeared to have suggested futility, so the study was closed to accrual. Among the 517 participants who were randomized (median age, 9 years [range, 0-26 years]; 44% female), 508 (98%) completed the trial. The 23 proven or probable invasive fungal disease events (6 caspofungin vs 17 fluconazole) included 14 molds, 7 yeasts, and 2 fungi not further categorized. The 5-month cumulative incidence of proven or probable invasive fungal disease was 3.1% (95% CI, 1.3%-7.0%) in the caspofungin group vs 7.2% (95% CI, 4.4%-11.8%) in the fluconazole group (overall P = .03 by log-rank test) and for cumulative incidence of proven or probable invasive aspergillosis was 0.5% (95% CI, 0.1%-3.5%) with caspofungin vs 3.1% (95% CI, 1.4%-6.9%) with fluconazole (overall P = .046 by log-rank test). No statistically significant differences in empirical antifungal therapy (71.9% caspofungin vs 69.5% fluconazole, overall P = .78 by log-rank test) or 2-year overall survival (68.8% caspofungin vs 70.8% fluconazole, overall P = .66 by log-rank test) were observed. The most common toxicities were hypokalemia (22 caspofungin vs 13 fluconazole), respiratory failure (6 caspofungin vs 9 fluconazole), and elevated alanine transaminase (4 caspofungin vs 8 fluconazole). Among children, adolescents, and young adults with acute myeloid leukemia, prophylaxis with caspofungin compared with fluconazole resulted in significantly lower incidence of invasive fungal disease. The findings suggest that caspofungin may be considered for prophylaxis against invasive fungal disease, although study interpretation is limited by early termination due to an unplanned interim analysis that appeared to have suggested futility. ClinicalTrials.gov Identifier: NCT01307579.

Identifiants

pubmed: 31688884
pii: 2753898
doi: 10.1001/jama.2019.15702
pmc: PMC6865545
doi:

Substances chimiques

Antifungal Agents 0
Fluconazole 8VZV102JFY
Caspofungin F0XDI6ZL63

Banques de données

ClinicalTrials.gov
['NCT01307579']

Types de publication

Clinical Trial, Phase III Comparative Study Journal Article Multicenter Study Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1673-1681

Subventions

Organisme : NCI NIH HHS
ID : K12 CA090625
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180886
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180899
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA189955
Pays : United States

Commentaires et corrections

Type : CommentIn

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Auteurs

Brian T Fisher (BT)

Division of Pediatrics Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Theoklis Zaoutis (T)

Division of Pediatrics Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Christopher C Dvorak (CC)

Division of Pediatric Allergy, Immunology and Bone Marrow Transplant, University of California San Francisco.

Michael Nieder (M)

Division of Blood and Marrow Transplant and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, Florida.

Danielle Zerr (D)

Division of Pediatric Infectious Diseases, Seattle Children's Hospital, Seattle, Washington.

John R Wingard (JR)

University of Florida College of Medicine, Gainesville.

Colleen Callahan (C)

Division of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Doojduen Villaluna (D)

Children's Oncology Group, Monrovia, California.

Lu Chen (L)

Division of Biostatistics, City of Hope, Duarte, California.

Ha Dang (H)

Department of Preventive Medicine, University of Southern California, Los Angeles.

Adam J Esbenshade (AJ)

Division of Pediatric Hematology and Oncology, Vanderbilt University Medical Center, Nashville, Tennessee.

Sarah Alexander (S)

Division of Haematology Oncology, The Hospital for Sick Children, Toronto, Ontario, Canada.

Joseph M Wiley (JM)

Division of Pediatric Hematology and Oncology, Sinai Hospital of Baltimore, Baltimore, Maryland.

Lillian Sung (L)

Division of Haematology Oncology, The Hospital for Sick Children, Toronto, Ontario, Canada.

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Classifications MeSH