TY - JOUR
T1 - Clinical Practice Guideline for the Therapeutic Drug Monitoring of Voriconazole in Non-Asian and Asian Adult Patients
T2 - Consensus Review by the Japanese Society of Chemotherapy and the Japanese Society of Therapeutic Drug Monitoring
AU - Japanese Antimicrobial Therapeutic Drug Monitoring Guideline Committee
AU - Takesue, Yoshio
AU - Hanai, Yuki
AU - Oda, Kazutaka
AU - Hamada, Yukihiro
AU - Ueda, Takashi
AU - Mayumi, Toshihiko
AU - Matsumoto, Kazuaki
AU - Fujii, Satoshi
AU - Takahashi, Yoshiko
AU - Miyazaki, Yoshitsugu
AU - Kimura, Toshimi
N1 - Funding Information:
This work was supported in part by the Research Program on Emerging and Re-emerging Infectious Diseases of the Japan Agency for Medical Research and Development grants 22fk0108135h0803 and 21fk0108135h0802. The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Funding Information:
We thank Victoria Muir, PhD, and Analisa Avila, MPH, ELS, from Edanz (https://jp.edanz.com/ac) for editing a draft of the manuscript. Author contributions are as follows: conceptualization: Yoshio Takesue, Yuki Hanai, Kazutaka Oda, and Yukihiro Hamada; data curation: Yoshio Takesue, Yuki Hanai, and Takashi Ueda; formal analysis: Yoshio Takesue, Yuki Hanai, and Takashi Ueda; funding acquisition: Yoshio Takesue and Yoshitsugu Miyazaki; investigation: Yuki Hanai, Kazutaka Oda, Yukihiro Hamada, Takashi Ueda, Toshihiko Mayumi, Kazuaki Matsumoto, Satoshi Fujii, Yoshiko Takahashi, and Toshimi Kimura; methodology: Yoshio Takesue, Yuki Hanai, Kazutaka Oda, Yukihiro Hamada, and Takashi Ueda; project administration: Yoshio Takesue, Yuki Hanai, and Toshimi Kimura Toshimi Kimura; resources: Yoshio Takesue, Yuki Hanai, Kazutaka Oda, Yukihiro Hamada, and Takashi Ueda; software: Yoshio Takesue and Yuki Hanai; supervision: Toshimi Kimura; validation: Yoshio Takesue and Yuki Hanai; visualization: Yoshio Takesue and Yuki Hanai; writing–original draft preparation: Yoshio Takesue, Yuki Hanai, Kazutaka Oda, Yukihiro Hamada, and Takashi Ueda; writing–review and editing: Yoshio Takesue, Yuki Hanai, Kazutaka Oda, Yukihiro Hamada, and Takashi Ueda. All authors have read and agreed to the published version of the manuscript.
Publisher Copyright:
© 2022 The Author(s)
PY - 2022/12
Y1 - 2022/12
N2 - Purpose: Voriconazole, an antifungal drug, is metabolized by a cytochrome P450 isozyme. Increased adverse effects are observed in Asians because of the high rate of poor metabolizers. In this therapeutic drug monitoring (TDM) guideline, recommendations were made according to ethnic group. Methods: Five clinical questions were used. For the preparation of the guideline, the performance of TDM in multicenter studies was surveyed (study 1). We also conducted a systematic review and meta-analysis (study 2) to establish recommendations for non-Asians and Asians. Findings: In study 1, 401 patients were surveyed. A risk of supratherapeutic concentrations was found in Japanese patients who adhered to the recommended dose. Target trough levels were achieved in 87% of patients with dose reductions. Although the trough level measured at the onset of adverse effects (AEs) was significantly associated with hepatotoxicity, no significant correlation was found between the initial trough level and hepatotoxicity, which indicated that hepatotoxicity was successfully prevented by the trough-guided dosing. In study 2, 22 studies (11 Asian locations and 11 non-Asian locations) were included in meta-analysis for the relationship between trough cutoff level (3, 4, 5, 5.5, and 6 µg/mL) and AEs. Significant differences were found for all cutoff levels, with the highest odds ratio for 4.0 µg/mL in Asian locations. In contrast, in non-Asian locations, no more than 1 study was available for any trough cutoff level, except for 5.5 µg/mL, at which level a significant increase in AEs was found. These findings indicate that TDM is strongly recommended to prevent AEs in Asians, and TDM is generally recommended for non-Asians to address subtherapeutic concentrations. TDM on day 3 is recommended to assess pharmacokinetic properties, including loading and maintenance doses. If the patient condition permits, delaying until day 5 is suggested for Asians because of the prolonged t½ in poor metabolizers. A trough level ≥1.0 µg/mL is strongly recommended to improve efficacy. Trough levels ≥2.0 µg/mL are suggested for invasive aspergillosis. To decrease adverse effects, trough levels <4.0 µg/mL are strongly recommended in Asians, whereas trough levels <5.5 µg/mL are generally recommended in non-Asians. Maintenance doses of 4 and 3 mg/kg twice daily are recommended in non-Asians and Asians, respectively. Implications: Different indications, timings, and target trough levels for TDM and different regimens are suggested for Asians and non-Asians.
AB - Purpose: Voriconazole, an antifungal drug, is metabolized by a cytochrome P450 isozyme. Increased adverse effects are observed in Asians because of the high rate of poor metabolizers. In this therapeutic drug monitoring (TDM) guideline, recommendations were made according to ethnic group. Methods: Five clinical questions were used. For the preparation of the guideline, the performance of TDM in multicenter studies was surveyed (study 1). We also conducted a systematic review and meta-analysis (study 2) to establish recommendations for non-Asians and Asians. Findings: In study 1, 401 patients were surveyed. A risk of supratherapeutic concentrations was found in Japanese patients who adhered to the recommended dose. Target trough levels were achieved in 87% of patients with dose reductions. Although the trough level measured at the onset of adverse effects (AEs) was significantly associated with hepatotoxicity, no significant correlation was found between the initial trough level and hepatotoxicity, which indicated that hepatotoxicity was successfully prevented by the trough-guided dosing. In study 2, 22 studies (11 Asian locations and 11 non-Asian locations) were included in meta-analysis for the relationship between trough cutoff level (3, 4, 5, 5.5, and 6 µg/mL) and AEs. Significant differences were found for all cutoff levels, with the highest odds ratio for 4.0 µg/mL in Asian locations. In contrast, in non-Asian locations, no more than 1 study was available for any trough cutoff level, except for 5.5 µg/mL, at which level a significant increase in AEs was found. These findings indicate that TDM is strongly recommended to prevent AEs in Asians, and TDM is generally recommended for non-Asians to address subtherapeutic concentrations. TDM on day 3 is recommended to assess pharmacokinetic properties, including loading and maintenance doses. If the patient condition permits, delaying until day 5 is suggested for Asians because of the prolonged t½ in poor metabolizers. A trough level ≥1.0 µg/mL is strongly recommended to improve efficacy. Trough levels ≥2.0 µg/mL are suggested for invasive aspergillosis. To decrease adverse effects, trough levels <4.0 µg/mL are strongly recommended in Asians, whereas trough levels <5.5 µg/mL are generally recommended in non-Asians. Maintenance doses of 4 and 3 mg/kg twice daily are recommended in non-Asians and Asians, respectively. Implications: Different indications, timings, and target trough levels for TDM and different regimens are suggested for Asians and non-Asians.
KW - fungal infection
KW - gene phenotype guideline
KW - therapeutic drug monitoring
KW - voriconazole
UR - http://www.scopus.com/inward/record.url?scp=85142871944&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85142871944&partnerID=8YFLogxK
U2 - 10.1016/j.clinthera.2022.10.005
DO - 10.1016/j.clinthera.2022.10.005
M3 - Review article
C2 - 36424314
AN - SCOPUS:85142871944
SN - 0149-2918
VL - 44
SP - 1604
EP - 1623
JO - Clinical Therapeutics
JF - Clinical Therapeutics
IS - 12
ER -