Biology of Blood and Marrow Transplantation
Volume 12, Issue 5 , Pages 552-559, May 2006

Voriconazole and Sirolimus Coadministration after Allogeneic Hematopoietic Stem Cell Transplantation

  • Francisco M. Marty

      Affiliations

    • Division of Infectious Diseases, Brigham & Women’s Hospital, Boston, Massachusetts, USA
    • Dana-Farber Cancer Institute, Boston, Massachusetts, USA
    • Harvard Medical School, Boston, Massachusetts, USA
    • Corresponding Author InformationCorrespondence and reprint requests: Francisco M. Marty, MD, Division of Infectious Diseases, Brigham & Women’s Hospital, 75 Francis St., PBB-A4, Boston, MA 02115
  • ,
  • Colleen M. Lowry

      Affiliations

    • Department of Pharmacy, Brigham & Women’s Hospital, Boston, Massachusetts, USA
  • ,
  • Corey S. Cutler

      Affiliations

    • Dana-Farber Cancer Institute, Boston, Massachusetts, USA
    • Harvard Medical School, Boston, Massachusetts, USA
    • Division of Medical Oncology, Brigham & Women’s Hospital, Boston, Massachusetts
  • ,
  • Bonnie J. Campbell

      Affiliations

    • Department of Pharmacy, Brigham & Women’s Hospital, Boston, Massachusetts, USA
  • ,
  • Karen Fiumara

      Affiliations

    • Department of Pharmacy, Brigham & Women’s Hospital, Boston, Massachusetts, USA
  • ,
  • Lindsey R. Baden

      Affiliations

    • Division of Infectious Diseases, Brigham & Women’s Hospital, Boston, Massachusetts, USA
    • Dana-Farber Cancer Institute, Boston, Massachusetts, USA
    • Harvard Medical School, Boston, Massachusetts, USA
  • ,
  • Joseph H. Antin

      Affiliations

    • Dana-Farber Cancer Institute, Boston, Massachusetts, USA
    • Harvard Medical School, Boston, Massachusetts, USA
    • Division of Medical Oncology, Brigham & Women’s Hospital, Boston, Massachusetts

Received 4 November 2005; accepted 12 December 2005.

Abstract 

Sirolimus is increasingly used in transplantation for prevention and treatment of graft-versus-host disease and organ rejection. Voriconazole is contraindicated when used concomitantly with sirolimus because of a substantial increase in sirolimus drug exposure with unadjusted dosing, but voriconazole is also considered the best initial treatment of invasive aspergillosis and other fungal infections. Patients who received voriconazole and sirolimus concomitantly were identified by a review of the medical records of all allogeneic hematopoietic stem cell recipients at our institution from September 1, 2002, to June 1, 2005. Data including baseline characteristics, indications for both drugs, and potential adverse effects were evaluated. Eleven patients received voriconazole and sirolimus concomitantly for a median of 33 days (range, 3-100 days). In 8 patients whose sirolimus dose was initially reduced by 90%, trough sirolimus levels were similar to those obtained before the administration of voriconazole; no obvious significant toxicity from either drug was observed during coadministration. Serious adverse events were observed in 2 patients in whom sirolimus dosing was not adjusted during voriconazole administration. Sirolimus and voriconazole may be safely coadministered if there is an empiric initial 90% sirolimus dose reduction combined with systematic monitoring of trough levels.

Key words:  Voriconazole , Sirolimus , Transplantation , Aspergillosis , Fungal infection

 

PII: S1083-8791(05)01414-X

doi:10.1016/j.bbmt.2005.12.032

Biology of Blood and Marrow Transplantation
Volume 12, Issue 5 , Pages 552-559, May 2006