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Leuk Res Treatment. 2017;2017:3460892. doi: 10.1155/2017/3460892. Epub 2017 Jun 11.

Evaluation of Serum Posaconazole Concentrations in Patients with Hematological Malignancies Receiving Posaconazole Suspension Compared to the Delayed-Release Tablet Formulation.

Leukemia research and treatment

Morgan Belling, Abraham S Kanate, Alexandra Shillingburg, Xiaoxiao Lu, Sijin Wen, Nilay Shah, Michael Craig, Aaron Cumpston

Affiliations

  1. Department of Pharmacy, West Virginia University Hospitals, Morgantown, WV, USA.
  2. Osborn Hematopoietic Malignancy and Transplantation Program, MBRCC, West Virginia University, Morgantown, WV, USA.
  3. Department of Biostatistics, West Virginia University, Morgantown, WV, USA.

PMID: 28695013 PMCID: PMC5485328 DOI: 10.1155/2017/3460892

Abstract

Posaconazole (PCZ) is frequently used for prophylaxis against invasive fungal infections (IFI) in patients undergoing induction chemotherapy for acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS). Posaconazole is commercially available as an oral suspension (PCZ-susp) and as a delayed-release tablet (PCZ-tab). Differences in absorption and bioavailability between these formulations may result in variability in serum posaconazole concentrations. The primary objective of this retrospective analysis was to compare attainment of goal serum posaconazole steady state concentrations (

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