Isavuconazole Versus Caspofungin in the Treatment of Candidemia and Other Invasive Candida Infections: The ACTIVE Trial.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
30 05 2019
Historique:
received: 22 05 2018
accepted: 04 10 2018
pubmed: 6 10 2018
medline: 29 7 2020
entrez: 6 10 2018
Statut: ppublish

Résumé

Isavuconazole was compared to caspofungin followed by oral voriconazole in a Phase 3, randomized, double-blind, multinational clinical trial for the primary treatment of patients with candidemia or invasive candidiasis. Adult patients were randomized 1:1 to isavuconazole (200 mg intravenous [IV] three-times-daily [TID] for 2 days, followed by 200 mg IV once-daily [OD]) or caspofungin (70 mg IV OD on day 1, followed by 50 mg IV OD [70 mg in patients > 80 kg]) for a maximum of 56 days. After day 10, patients could switch to oral isavuconazole (isavuconazole arm) or voriconazole (caspofungin arm). Primary efficacy endpoint was successful overall response at the end of IV therapy (EOIVT) in patients with proven infections who received ≥1 dose of study drug (modified-intent-to-treat [mITT] population). The pre-specified noninferiority margin was 15%. Secondary outcomes in the mITT population were successful overall response at 2 weeks after the end of treatment, all-cause mortality at days 14 and 56, and safety. Of 450 patients randomized, 400 comprised the mITT population. Baseline characteristics were balanced between groups. Successful overall response at EOIVT was observed in 60.3% of patients in the isavuconazole arm and 71.1% in the caspofungin arm (adjusted difference -10.8, 95% confidence interval -19.9--1.8). The secondary endpoints, all-cause mortality, and safety were similar between arms. Median time to clearance of the bloodstream was comparable between groups. This study did not demonstrate non-inferiority of isavuconazole to caspofungin for primary treatment of invasive candidiasis. Secondary endpoints were similar between both groups. NCT00413218.

Sections du résumé

BACKGROUND
Isavuconazole was compared to caspofungin followed by oral voriconazole in a Phase 3, randomized, double-blind, multinational clinical trial for the primary treatment of patients with candidemia or invasive candidiasis.
METHODS
Adult patients were randomized 1:1 to isavuconazole (200 mg intravenous [IV] three-times-daily [TID] for 2 days, followed by 200 mg IV once-daily [OD]) or caspofungin (70 mg IV OD on day 1, followed by 50 mg IV OD [70 mg in patients > 80 kg]) for a maximum of 56 days. After day 10, patients could switch to oral isavuconazole (isavuconazole arm) or voriconazole (caspofungin arm). Primary efficacy endpoint was successful overall response at the end of IV therapy (EOIVT) in patients with proven infections who received ≥1 dose of study drug (modified-intent-to-treat [mITT] population). The pre-specified noninferiority margin was 15%. Secondary outcomes in the mITT population were successful overall response at 2 weeks after the end of treatment, all-cause mortality at days 14 and 56, and safety.
RESULTS
Of 450 patients randomized, 400 comprised the mITT population. Baseline characteristics were balanced between groups. Successful overall response at EOIVT was observed in 60.3% of patients in the isavuconazole arm and 71.1% in the caspofungin arm (adjusted difference -10.8, 95% confidence interval -19.9--1.8). The secondary endpoints, all-cause mortality, and safety were similar between arms. Median time to clearance of the bloodstream was comparable between groups.
CONCLUSIONS
This study did not demonstrate non-inferiority of isavuconazole to caspofungin for primary treatment of invasive candidiasis. Secondary endpoints were similar between both groups.
CLINICAL TRIALS REGISTRATION
NCT00413218.

Identifiants

pubmed: 30289478
pii: 5115695
doi: 10.1093/cid/ciy827
doi:

Substances chimiques

Nitriles 0
Pyridines 0
Triazoles 0
isavuconazole 60UTO373KE
Caspofungin F0XDI6ZL63

Banques de données

ClinicalTrials.gov
['NCT00413218']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1981-1989

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2018. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Auteurs

Bart Jan Kullberg (BJ)

Radboud Center for Infectious Diseases, and Department of Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.

Claudio Viscoli (C)

Dipartimento di Scienze della Salute, University of Genova.
Ospedale Policlinico San Martino, Genova, Italy.

Peter G Pappas (PG)

University of Alabama at Birmingham.

Jose Vazquez (J)

Medical College of Georgia/Augusta University.

Luis Ostrosky-Zeichner (L)

University of Texas, Houston.

Coleman Rotstein (C)

University Health Network, University of Toronto, Ontario, Canada.

Jack D Sobel (JD)

Wayne State University, Detroit, Michigan.

Raoul Herbrecht (R)

Hôpitaux Universitaires de Strasbourg and Université de Strasbourg, Inserm, UMR-S1113/IRFAC, France.

Galia Rahav (G)

Sheba Medical Center and Sackler Faculty of Medicine, Tel Aviv University, Israel.

Sutep Jaruratanasirikul (S)

Songklanagarind Hospital, Hat Yai.

Ploenchan Chetchotisakd (P)

Srinagarind Hospital, Khon Kaen University, Thailand.

Eric Van Wijngaerden (E)

Ku Leuven, Belgium.

Jan De Waele (J)

Ghent University Hospital, Belgium.

Christopher Lademacher (C)

Astellas Pharma Global Development, Inc, Northbrook, Illinois.

Marc Engelhardt (M)

Basilea Pharmaceutica International Ltd., Basel, Switzerland.

Laura Kovanda (L)

Astellas Pharma Global Development, Inc, Northbrook, Illinois.

Rodney Croos-Dabrera (R)

Astellas Pharma Global Development, Inc, Northbrook, Illinois.

Christine Fredericks (C)

Astellas Pharma Global Development, Inc, Northbrook, Illinois.

George R Thompson (GR)

Department of Medicine, University of California Davis.

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Classifications MeSH