Caspofungin exposure-response relationships in adult patients with mucosal or invasive candidiasis

• Published in: Clinical pharmacology in drug development Vol. 3; no. 1; pp. 43 - 50
• Main Authors: Comisar, Wendy, Sun, Peng, Li, Susan, Sable, Carole, Schwartz, Michael, Bi, Sheng, Chow, Joseph, Ngai, Angela, Winchell, Gregory, Kartsonis, Nicholas, Stone, Julie
• Format: Journal Article
• Language: English
• Published: United States Blackwell Publishing Ltd 01-01-2014; Wiley Subscription Services, Inc
• Subjects: caspofungin; invasive candidiasis; mucosal candidiasis; pharmacodynamics; pharmacokinetics; invasive candidiasis; mucosal candidiasis; pharmacokinetics; caspofungin; pharmacodynamics
• ISSN: 2160-763X; 2160-7648
• DOI: 10.1002/cpdd.44

Caspofungin is an echinocandin antifungal agent administered once daily as an intravenous infusion. Relationships between caspofungin exposure and clinical efficacy and safety were investigated. End‐of‐infusion (CEOI) and trough (C24 hours) concentrations were obtained in 218 patients with mucosal (i.e., esophageal and/or oropharyngeal) candidiasis (MC) receiving caspofungin 35, 50, or 70 mg/day and 278 patients with invasive candidiasis (IC) receiving 50, 100, or 150 mg/day. Area under the plasma concentration–time curve (AUC0–24 hours) was obtained in a subset of MC patients (n = 99). Odds ratios were estimated for the association between log‐transformed PK and efficacy response and the occurrence of common adverse events. No pharmacokinetic or hybrid parameter (ratio of AUC:MIC, CEOI:MIC, C24 hours:MIC) was significantly correlated with overall treatment outcome in either MC or IC, although this patient population may exhibit confounding factors which masked a potential pharmacokinetic/pharmacodynamic relationship. An exploratory evaluation of MC identified significant pharmacokinetic correlations with endoscopic response, but not symptom response. Statistically significant associations were identified for IC patients with C. parapsilosis infections. Occurrence of clinical adverse events and/or laboratory abnormalities did not appear to be increased by higher caspofungin plasma concentrations. Caspofungin concentrations achieved with 50 mg/day are generally within the therapeutic window for the treatment of candidiasis.