Treatment of invasive aspergillosis with posaconazole in patients who are refractory to or intolerant of conventional therapy: An externally controlled trial

被引:563
作者
Walsh, Thomas J.
Raad, Issam
Patterson, Thomas F.
Chandrasekar, Pranatharthi
Donowitz, Gerald R.
Graybill, Richard
Greene, Reginald E.
Hachem, Ray
Hadley, Susan
Herbrecht, Raoul
Langston, Amelia
Louie, Arnold
Ribaud, Patricia
Segal, Brahm H.
Stevens, David A.
van Burik, Jo-Anne H.
White, Charles S.
Corcoran, Gavin
Gogate, Jagadish
Krishna, Gopal
Pedicone, Lisa
Hardalo, Catherine
Perfect, John R.
机构
[1] NCI, Immunocompromised Host Sect, Bethesda, MD 20892 USA
[2] Univ Maryland, Baltimore, MD 21201 USA
[3] Univ Texas, MD Anderson Canc Ctr, Houston, TX 77030 USA
[4] Univ Texas, Hlth Sci Ctr, San Antonio, TX 78285 USA
[5] Wayne State Univ, Detroit, MI USA
[6] Univ Virginia, Charlottesville, VA USA
[7] Massachusetts Gen Hosp, Boston, MA 02114 USA
[8] Tufts Univ New England Med Ctr, Boston, MA 02111 USA
[9] Emory Univ Hosp, Atlanta, GA 30322 USA
[10] Albany Med Ctr, Albany, NY USA
[11] Roswell Pk Mem Canc Ctr, Buffalo, NY USA
[12] Santa Clara Valley Med Ctr, San Jose, CA 95128 USA
[13] Univ Minnesota, Sch Med, Minneapolis, MN USA
[14] Schering Plough Res Inst, Kenilworth, NJ USA
[15] Duke Univ, Durham, NC USA
[16] Hop Hautepierre, Strasbourg, France
[17] Hosp St Louis, Paris, France
关键词
D O I
10.1086/508774
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Invasive aspergillosis is an important cause of morbidity and mortality in immunocompromised patients. Current treatments provide limited benefit. Posaconazole is an extended-spectrum triazole with in vitro and in vivo activity against Aspergillus species. Methods. We investigated the efficacy and safety of posaconazole oral suspension (800 mg/day in divided doses) as monotherapy in an open-label, multicenter study in patients with invasive aspergillosis and other mycoses who were refractory to or intolerant of conventional antifungal therapy. Data from external control cases were collected retrospectively to provide a comparative reference group. Results. Cases of aspergillosis deemed evaluable by a blinded data review committee included 107 posaconazole recipients and 86 control subjects (modified intent-to-treat population). The populations were similar and balanced with regard to prespecified demographic and disease variables. The overall success rate (i.e., the data review committee-assessed global response at the end of treatment) was 42% for posaconazole recipients and 26% for control subjects (odds ratio, 4.06; 95% confidence interval, 1.50-11.04;). The differences in response Pp. 006 between the modified intent-to-treat treatment groups were preserved across additional, prespecified subsets, including infection site (pulmonary or disseminated), hematological malignancy, hematopoietic stem cell transplantation, baseline neutropenia, and reason for enrollment(patient was refractory to or intolerant of previous antifungal therapy). An exposure-response relationship was suggested by pharmacokinetic analyses. Conclusions. Although the study predates extensive use of echinocandins and voriconazole, these findings demonstrate that posaconazole is an alternative to salvage therapy for patients with invasive aspergillosis who are refractory to or intolerant of previous antifungal therapy.
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页码:2 / 12
页数:11
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