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泊沙康唑口服混悬液在血液系统恶性肿瘤患者中的早期治疗药物监测

Early Therapeutic Drug Monitoring of Posaconazole Oral Suspension in Patients With Hematologic Malignancies.

作者信息

Suh Hyeon Jeong, Kim Inho, Cho Joo-Youn, Park Sang-In, Yoon Seo Hyun, Hwang Joo-Hee, Bae Ji Yun, Lee Jeong-Ok, Koh Youngil, Song Kyoung-Ho, Choe Pyoeng Gyun, Yu Kyung-Sang, Kim Eu Suk, Kim Hong Bin, Bang Soo-Mee, Kim Nam Joong, Song Sang Hoon, Park Wan Beom, Oh Myoung-Don

机构信息

Departments of Internal Medicine and.

Clinical Pharmacology and Therapeutics, Seoul National University Hospital, Seoul National University College of Medicine.

出版信息

Ther Drug Monit. 2018 Feb;40(1):115-119. doi: 10.1097/FTD.0000000000000469.

Abstract

BACKGROUND

Therapeutic drug monitoring (TDM) of posaconazole is usually performed 1 week after starting the drug because of its long half-life. However, previous studies showed that measuring the posaconazole plasma concentration (PPC) on day 3 is effective for predicting steady-state levels. The purpose of this study was to evaluate the relevance of early TDM (day 3) of posaconazole for achieving an optimal PPC.

METHODS

This prospective study was conducted from September 2014 to August 2016. A total of 148 patients with acute myeloid leukemia or myelodysplastic syndromes received a 200 mg posaconazole oral suspension 3 times daily for fungal prophylaxis. During the period from September 2014 to December 2015 (control group), no dose adjustment was performed on day 3. During the period from January 2016 to Aug 2016 (early TDM group), the frequency of posaconazole 200-mg administration was increased to 4 times daily in patients whose PPC on day 3 was <400 ng/mL. The cutoff value for optimal PPC on day 8 was defined as 500 ng/mL.

RESULTS

In 21 of 107 patients (20%) in the control group, PPC was <400 ng/mL on day 3. In 15 (71%) of these 21 patients, the PPC was suboptimal on day 8. In the early TDM group, the PPC was <400 ng/mL on day 3 in 4 of 41 patients (10%). After increasing the posaconazole administration frequency in these 4 patients, PPC was suboptimal on day 8 in 1 patient (25%). In both groups, 104 patients had a PPC of ≥500 ng/mL on day 3, but 7% (7/104) of these had a suboptimal level on day 8.

CONCLUSIONS

Early TDM on day 3 for posaconazole suspension may help more patients achieve optimal drug levels on day 8, although TDM on day 8 is needed even in patients with optimal levels on day 3.

摘要

背景

由于泊沙康唑半衰期长,其治疗药物监测(TDM)通常在开始用药1周后进行。然而,既往研究表明,在第3天测定泊沙康唑血药浓度(PPC)对预测稳态水平有效。本研究旨在评估泊沙康唑早期TDM(第3天)与达到最佳PPC的相关性。

方法

本前瞻性研究于2014年9月至2016年8月进行。共148例急性髓系白血病或骨髓增生异常综合征患者接受200mg泊沙康唑口服混悬液,每日3次用于预防真菌感染。在2014年9月至2015年12月期间(对照组),第3天未进行剂量调整。在2016年1月至2016年8月期间(早期TDM组),第3天PPC<400ng/mL的患者,泊沙康唑200mg给药频率增加至每日4次。第8天最佳PPC的临界值定义为500ng/mL。

结果

对照组107例患者中有21例(20%)第3天PPC<400ng/mL。这21例患者中有15例(71%)第8天PPC未达最佳水平。在早期TDM组,41例患者中有4例(10%)第3天PPC<400ng/mL。这4例患者增加泊沙康唑给药频率后,1例患者(25%)第8天PPC未达最佳水平。两组中,104例患者第3天PPC≥500ng/mL,但其中7%(7/104)第8天水平未达最佳。

结论

泊沙康唑混悬液第3天进行早期TDM可能有助于更多患者在第8天达到最佳药物水平,尽管第3天水平最佳的患者也需要在第8天进行TDM。

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