Back to Search Start Over

Phase II Dose Escalation Study of Caspofungin for Invasive Aspergillosis

Authors :
Cornely, O. A.
Vehreschild, J. J.
Vehreschild, M. J. G. T.
Würthwein, G.
Arenz, D.
Schwartz, S.
Heussel, C. P.
Silling, G.
Mahne, M.
Franklin, J.
Harnischmacher, U.
Wilkens, A.
Farowski, F.
Karthaus, M.
Lehrnbecher, T.
Ullmann, A. J.
Hallek, M.
Groll, A. H.
Source :
Antimicrobial Agents and Chemotherapy; September 2011, Vol. 55 Issue: 12 p5798-5803, 6p
Publication Year :
2011

Abstract

ABSTRACTOur objective was to evaluate the maximum tolerated dose of caspofungin for invasive aspergillosis (IA). The safety and pharmacokinetics of escalating dosages of caspofungin were investigated in IA. Eight patients each received caspofungin 70, 100, 150, or 200 mg once a day (QD). Dose-limiting toxicity (DLT) was defined as the same non-hematological treatment-related adverse event of grade ≥4 in 2 of 8 patients or ≥3 in 4 of 8 patients in a cohort. A total of 46 patients (median age, 61 years; 21 female; 89% with hematological malignancies) received caspofungin (9, 8, 9, and 20 patients in the 70-, 100-, 150-, and 200-mg cohorts) for a median of 24.5 days. Plasma pharmacokinetics were linear across the investigated dosages and followed a two-compartment model, with weight as the covariate on clearance and sex as the covariate on central volume of distribution. Simulated peak plasma concentrations at steady state ranged from 14.2 to 40.6 mg/liter (28%), trough concentrations from 4.1 to 11.8 mg/liter (58%), and area under the concentration-time curve from 175 to 500 mg/liter/h (32%) (geometric mean, geometric coefficient of variation). Treatment was well tolerated without dose-limiting toxicity. The rate of complete or partial responses was 54.3%, and the overall mortality at 12-week follow-up was 28.3%. In first-line treatment of invasive aspergillosis, daily doses of up to 200 mg caspofungin were well tolerated and the maximum tolerated dose was not reached. Pharmacokinetics was linear. Response rates were similar to those previously reported for voriconazole and liposomal amphotericin.

Details

Language :
English
ISSN :
00664804 and 10986596
Volume :
55
Issue :
12
Database :
Supplemental Index
Journal :
Antimicrobial Agents and Chemotherapy
Publication Type :
Periodical
Accession number :
ejs57155593
Full Text :
https://doi.org/10.1128/AAC.05134-11