101. Safety, clinical effectiveness and trough plasma concentrations of intravenous posaconazole in patients with haematological malignancies and/or undergoing allogeneic haematopoietic stem cell transplantation: off-trial experience
- Author
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Andrew Grigg, Wirawan Jeong, Peter Haywood, Monica A. Slavin, Julian Lindsay, Anton Y. Peleg, Naranie Shanmuganathan, John F. Seymour, David C. M. Kong, Michelle Ananda-Rajah, Ashish Bajel, Sharon C.-A. Chen, David Ritchie, and Karen F Urbancic
- Subjects
Adult ,Male ,0301 basic medicine ,Microbiology (medical) ,medicine.medical_specialty ,Posaconazole ,Antifungal Agents ,Drug-Related Side Effects and Adverse Reactions ,medicine.medical_treatment ,030106 microbiology ,Hematopoietic stem cell transplantation ,Chemoprevention ,Plasma ,03 medical and health sciences ,Cmin ,0302 clinical medicine ,Internal medicine ,Amphotericin B ,Humans ,Transplantation, Homologous ,Medicine ,Pharmacology (medical) ,In patient ,030212 general & internal medicine ,Intensive care medicine ,Adverse effect ,Retrospective Studies ,Pharmacology ,business.industry ,Australia ,Hematopoietic Stem Cell Transplantation ,Retrospective cohort study ,Middle Aged ,Triazoles ,Transplantation ,Treatment Outcome ,Infectious Diseases ,Mycoses ,Hematologic Neoplasms ,Administration, Intravenous ,Female ,business ,medicine.drug - Abstract
Objectives This study describes the safety, clinical effectiveness and trough plasma concentration (Cmin) of intravenous (iv) posaconazole, provided as part of Merck Sharp and Dohme Australia's Named Patient Programme (NPP) in non-clinical trial settings. Methods A multicentre, retrospective study on the NPP use of iv posaconazole between July 2014 and March 2015 across seven Australian hospitals. Results Seventy courses of iv posaconazole were prescribed and evaluated in 61 patients receiving treatment for haematological malignancy. Sixty-one courses were prescribed for prophylaxis against invasive fungal disease (IFD), the majority of which (59) were initiated in patients with gastrointestinal disturbances and/or intolerance to previous antifungals. The median (IQR) duration for prophylaxis was 10 (6-15) days. No breakthrough IFD was observed during or at cessation of iv posaconazole. Nine courses of iv posaconazole were prescribed for treatment of IFD with a median (IQR) duration of 19 (7-30) days. Improvement in signs and symptoms of IFD was observed in five cases at cessation of, and six cases at 30 days post-iv posaconazole. Cmin was measured in 39 courses of iv posaconazole, with the initial level taken [median (IQR)] 4 (3-7) days after commencing iv posaconazole. The median (IQR) of initial Cmin was 1.16 (0.69-2.06) mg/L. No severe adverse events specifically attributed to iv posaconazole were documented, although six courses were curtailed due to potential toxicity. Conclusions This non-clinical trial experience suggests that iv posaconazole appeared to be safe and clinically effective for prophylaxis or treatment of IFD in patients receiving treatment for haematological malignancies.
- Published
- 2016