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Published in: Journal of Cancer Research and Clinical Oncology 1/2018

01-01-2018 | Original Article – Clinical Oncology

Safety study and therapeutic drug monitoring of the oral tablet formulation of posaconazole in patients with haematological malignancies

Authors: C. Boglione-Kerrien, S. Picard, C. Tron, S. Nimubona, J.-P. Gangneux, S. Lalanne, F. Lemaitre, E. Bellissant, M.-C. Verdier, A. Petitcollin

Published in: Journal of Cancer Research and Clinical Oncology | Issue 1/2018

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Abstract

Purpose

Posaconazole is a triazole antifungal widely used for prophylaxis of invasive fungal disease (IFI). Posaconazole tablets allow reaching higher plasma levels than the oral suspension, but safety data with this formulation in real life are scarce. This study aimed at evaluating the safety profile, the pharmacokinetic variability, and the concentration–toxicity relationship of posaconazole tablets in patients with haematological malignancies.

Methods

Sixty neutropenic patients treated with posaconazole tablets for prophylaxis of IFI were prospectively included in the study. Adverse drug reactions (ADR) were recorded and analyzed by the Regional Pharmacovigilance Centre to assess posaconazole implication. Blood samples were drawn once a week and plasma trough concentrations (C min) were assayed by LC–MS/MS. The rates of ADR by quartile of C min were compared.

Results

Eighteen patients (30%) experienced at least one ADR attributed to posaconazole. Liver function test (LFT) abnormalities were encountered in 20% of patients and resulted in four (6.7%) treatment discontinuations. Posaconazole median (range) C min was 1.36 (< 0.1–3.44) µg/mL (inter-patient CV = 43.9%). During follow-up, 28.6% of patients had at least one concentration < 0.7 µg/mL, and 35.7% had at least one concentration > 2 µg/mL. Rates of ADR by quartile of C min were not different.

Conclusions

Posaconazole was well tolerated; however, LFT abnormalities were frequent. ADR occurrence was not linked to posaconazole exposure. Because posaconazole concentrations were highly variable, TDM can be helpful to avoid underexposure to the drug and increase its efficacy in preventing IFI. Conversely, a large proportion of patients was overexposed and might have benefited of a dose reduction.
Literature
go back to reference Ashbee HR, Barnes RA, Johnson EM et al (2014) Therapeutic drug monitoring (TDM) of antifungal agents: guidelines from the British Society for Medical Mycology. J Antimicrob Chemother 69:1162–1176. doi:10.1093/jac/dkt508 CrossRefPubMed Ashbee HR, Barnes RA, Johnson EM et al (2014) Therapeutic drug monitoring (TDM) of antifungal agents: guidelines from the British Society for Medical Mycology. J Antimicrob Chemother 69:1162–1176. doi:10.​1093/​jac/​dkt508 CrossRefPubMed
go back to reference Bégaud B, Evreux JC, Jouglard J, Lagier G (1985) Imputation of the unexpected or toxic effects of drugs. Actualization of the method used in France. Therapie 40:111–118PubMed Bégaud B, Evreux JC, Jouglard J, Lagier G (1985) Imputation of the unexpected or toxic effects of drugs. Actualization of the method used in France. Therapie 40:111–118PubMed
go back to reference Cornely OA, Duarte RF, Haider S et al (2016) Phase 3 pharmacokinetics and safety study of a posaconazole tablet formulation in patients at risk for invasive fungal disease. J Antimicrob Chemother 71:718–726. doi:10.1093/jac/dkv380 CrossRefPubMed Cornely OA, Duarte RF, Haider S et al (2016) Phase 3 pharmacokinetics and safety study of a posaconazole tablet formulation in patients at risk for invasive fungal disease. J Antimicrob Chemother 71:718–726. doi:10.​1093/​jac/​dkv380 CrossRefPubMed
go back to reference Courtney R, Pai S, Laughlin M et al (2003) Pharmacokinetics, safety, and tolerability of oral posaconazole administered in single and multiple doses in healthy adults. Antimicrob Agents Chemother 47:2788–2795CrossRefPubMedPubMedCentral Courtney R, Pai S, Laughlin M et al (2003) Pharmacokinetics, safety, and tolerability of oral posaconazole administered in single and multiple doses in healthy adults. Antimicrob Agents Chemother 47:2788–2795CrossRefPubMedPubMedCentral
go back to reference Jang SH, Colangelo PM, Gobburu JVS (2010) Exposure-response of posaconazole used for prophylaxis against invasive fungal infections: evaluating the need to adjust doses based on drug concentrations in plasma. Clin Pharmacol Ther 88:115–119. doi:10.1038/clpt.2010.64 CrossRefPubMed Jang SH, Colangelo PM, Gobburu JVS (2010) Exposure-response of posaconazole used for prophylaxis against invasive fungal infections: evaluating the need to adjust doses based on drug concentrations in plasma. Clin Pharmacol Ther 88:115–119. doi:10.​1038/​clpt.​2010.​64 CrossRefPubMed
go back to reference Miceli MH, Perissinotti AJ, Kauffman CA, Couriel DR (2015) Serum posaconazole levels among haematological cancer patients taking extended release tablets is affected by body weight and diarrhoea: single centre retrospective analysis. Mycoses 58:432–436. doi:10.1111/myc.12339 CrossRefPubMed Miceli MH, Perissinotti AJ, Kauffman CA, Couriel DR (2015) Serum posaconazole levels among haematological cancer patients taking extended release tablets is affected by body weight and diarrhoea: single centre retrospective analysis. Mycoses 58:432–436. doi:10.​1111/​myc.​12339 CrossRefPubMed
go back to reference Pettit NN, Steinback JL, Han Z, de la Cruz J, Landon E, Pisano J (2014) Posaconazole (PCZ) tablet formulation therapeutic drug monitoring (TDM) and toxicity analysis. In: Poster presented at 54th Interscience conference on antimicrobial agents and chemotherapy; Washington, DC Pettit NN, Steinback JL, Han Z, de la Cruz J, Landon E, Pisano J (2014) Posaconazole (PCZ) tablet formulation therapeutic drug monitoring (TDM) and toxicity analysis. In: Poster presented at 54th Interscience conference on antimicrobial agents and chemotherapy; Washington, DC
go back to reference Pham AN, Bubalo JS, Lewis JS (2016) Posaconazole tablet formulation at 400 milligrams daily achieves desired minimum serum concentrations in adult patients with a hematologic malignancy or stem cell transplant. Antimicrob Agents Chemother 60:6945–6947. doi:10.1128/AAC.01489-16 CrossRefPubMedPubMedCentral Pham AN, Bubalo JS, Lewis JS (2016) Posaconazole tablet formulation at 400 milligrams daily achieves desired minimum serum concentrations in adult patients with a hematologic malignancy or stem cell transplant. Antimicrob Agents Chemother 60:6945–6947. doi:10.​1128/​AAC.​01489-16 CrossRefPubMedPubMedCentral
go back to reference Raad II, Hachem RY, Herbrecht R et al (2006) Posaconazole as salvage treatment for invasive fusariosis in patients with underlying hematologic malignancy and other conditions. Clin Infect Dis Off Publ Infect Dis Soc Am 42:1398–1403. doi:10.1086/503425 CrossRef Raad II, Hachem RY, Herbrecht R et al (2006) Posaconazole as salvage treatment for invasive fusariosis in patients with underlying hematologic malignancy and other conditions. Clin Infect Dis Off Publ Infect Dis Soc Am 42:1398–1403. doi:10.​1086/​503425 CrossRef
go back to reference Verdier M-C, Bentué-Ferrer D, Tribut O, Bellissant E (2010) Liquid chromatography-tandem mass spectrometry method for simultaneous quantification of four triazole antifungal agents in human plasma. Clin Chem Lab Med 48:1515–1522. doi:10.1515/CCLM.2010.252 CrossRefPubMed Verdier M-C, Bentué-Ferrer D, Tribut O, Bellissant E (2010) Liquid chromatography-tandem mass spectrometry method for simultaneous quantification of four triazole antifungal agents in human plasma. Clin Chem Lab Med 48:1515–1522. doi:10.​1515/​CCLM.​2010.​252 CrossRefPubMed
Metadata
Title
Safety study and therapeutic drug monitoring of the oral tablet formulation of posaconazole in patients with haematological malignancies
Authors
C. Boglione-Kerrien
S. Picard
C. Tron
S. Nimubona
J.-P. Gangneux
S. Lalanne
F. Lemaitre
E. Bellissant
M.-C. Verdier
A. Petitcollin
Publication date
01-01-2018
Publisher
Springer Berlin Heidelberg
Published in
Journal of Cancer Research and Clinical Oncology / Issue 1/2018
Print ISSN: 0171-5216
Electronic ISSN: 1432-1335
DOI
https://doi.org/10.1007/s00432-017-2523-2

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