Infectious Diseases Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Medicine, Weill Cornell Medical College, New York, NY, USA.
Med Mycol. 2021 Oct 4;59(10):970-979. doi: 10.1093/mmy/myab025.
Voriconazole is frequently discontinued prematurely as primary antifungal prophylaxis (AFP) in allogeneic hematopoietic cell transplant (HCT) recipients due to adverse events. Limited data exists for isavuconazole as AFP. We analyzed adult HCT recipients who received voriconazole or isavuconazole AFP to estimate rate of premature AFP discontinuation, identify risk factors for premature AFP discontinuation, and compare incidence of invasive fungal infection (IFI) and survival at day + 180 post-HCT between patients who received voriconazole/isavuconazole-AFP. This was a propensity score matched cohort analysis of 210 HCT-recipients who received voriconazole-AFP (9/1/2014-12/31/2016; voriconazole-cohort), and 95 HCT-recipients who received isavuconazole-AFP (5/1/2017-10/31/2018; isavuconazole-cohort). AFP discontinuation for any reason prior to completion was defined as "premature". Median (interquartile range, IQR) duration of AFP was longer in the isavuconazole-cohort (94 days, 87-100) vs. the voriconazole-cohort (76 days, 23-94; P-value < 0.0001). Premature AFP discontinuation was more frequent in the voriconazole-cohort (92/210, 43.8%) vs. the isavuconazole-cohort (14/95, 14.7%; P-value < 0.0001). The most common reason for premature discontinuation was biochemical hepatotoxicity (voriconazole-cohort: 48/210, 22.8% vs. isavuconazole-cohort: 5/95, 5.26%; P-value = 0.0002). Transaminase values between baseline and end-of-treatment (EOT) and up to 14 days post-EOT significantly increased in the voriconazole-cohort, but remained unchanged in the isavuconazole-cohort. The incidence of IFI at day + 180 was 2.9% (6/210) and 3.2% (3/95) in the voriconazole-cohort and isavuconazole-cohort, respectively (P-value = 0.881). All-cause mortality at day + 180 was 2.4% (5/210) and 6.3% (6/95) in the voriconazole-cohort and isavuconazole-cohort, respectively (P-value = 0.089). When compared to voriconazole, isavuconazole was a safer and as effective primary AFP during the first 3 months after HCT.
When compared to voriconazole, isavuconazole is a safer and as effective primary antifungal prophylaxis during the first 3 months after allogeneic hematopoietic cell transplant, with lower rates of hepatotoxicity, and similar rates of fungal infections and all-cause mortality.
由于不良事件,伏立康唑常作为异基因造血细胞移植(HCT)受者的主要抗真菌预防(AFP)而提前过早停药。伊曲康唑作为 AFP 的应用数据有限。我们分析了接受伏立康唑或伊曲康唑 AFP 的成年 HCT 受者,以评估 AFP 提前过早停药的发生率,确定 AFP 提前过早停药的危险因素,并比较接受伏立康唑/伊曲康唑 AFP 的患者在 HCT 后第 180 天侵袭性真菌感染(IFI)和生存的发生率。这是对接受伏立康唑 AFP(2014 年 9 月 1 日至 2016 年 12 月 31 日;伏立康唑组)的 210 名 HCT 受者和接受伊曲康唑 AFP(2017 年 5 月 1 日至 2018 年 10 月 31 日;伊曲康唑组)的 95 名 HCT 受者进行的倾向评分匹配队列分析。在完成 AFP 之前,任何原因的 AFP 提前过早停药均定义为“提前过早”。伊曲康唑组 AFP 的中位(四分位距,IQR)持续时间较长(94 天,87-100)vs. 伏立康唑组(76 天,23-94;P 值<0.0001)。伏立康唑组 AFP 提前过早停药更为常见(92/210,43.8%)vs. 伊曲康唑组(14/95,14.7%;P 值<0.0001)。提前过早停药的最常见原因是生化性肝毒性(伏立康唑组:48/210,22.8% vs. 伊曲康唑组:5/95,5.26%;P 值=0.0002)。伏立康唑组的转氨酶值在基线和治疗结束(EOT)之间以及 EOT 后 14 天内显著增加,而伊曲康唑组的转氨酶值保持不变。伏立康唑组和伊曲康唑组在第 180 天的 IFI 发生率分别为 2.9%(6/210)和 3.2%(3/95)(P 值=0.881)。伏立康唑组和伊曲康唑组在第 180 天的全因死亡率分别为 2.4%(5/210)和 6.3%(6/95)(P 值=0.089)。与伏立康唑相比,伊曲康唑在 HCT 后 3 个月内作为主要 AFP 更安全、同样有效。
伏立康唑在异基因造血细胞移植(HCT)受者中常因不良事件而提前过早停止作为主要抗真菌预防(AFP)。伊曲康唑作为 AFP 的应用数据有限。我们分析了接受伏立康唑或伊曲康唑 AFP 的成年 HCT 受者,以评估 AFP 提前过早停药的发生率,确定 AFP 提前过早停药的危险因素,并比较接受伏立康唑/伊曲康唑 AFP 的患者在 HCT 后第 180 天侵袭性真菌感染(IFI)和生存的发生率。这是对接受伏立康唑 AFP(2014 年 9 月 1 日至 2016 年 12 月 31 日;伏立康唑组)的 210 名 HCT 受者和接受伊曲康唑 AFP(2017 年 5 月 1 日至 2018 年 10 月 31 日;伊曲康唑组)的 95 名 HCT 受者进行的倾向评分匹配队列分析。在完成 AFP 之前,任何原因的 AFP 提前过早停药均定义为“提前过早”。伊曲康唑组 AFP 的中位(四分位距,IQR)持续时间较长(94 天,87-100)vs. 伏立康唑组(76 天,23-94;P 值<0.0001)。伏立康唑组 AFP 提前过早停药更为常见(92/210,43.8%)vs. 伊曲康唑组(14/95,14.7%;P 值<0.0001)。提前过早停药的最常见原因是生化性肝毒性(伏立康唑组:48/210,22.8% vs. 伊曲康唑组:5/95,5.26%;P 值=0.0002)。伏立康唑组的转氨酶值在基线和治疗结束(EOT)之间以及 EOT 后 14 天内显著增加,而伊曲康唑组的转氨酶值保持不变。伏立康唑组和伊曲康唑组在第 180 天的 IFI 发生率分别为 2.9%(6/210)和 3.2%(3/95)(P 值=0.881)。伏立康唑组和伊曲康唑组在第 180 天的全因死亡率分别为 2.4%(5/210)和 6.3%(6/95)(P 值=0.089)。与伏立康唑相比,伊曲康唑在 HCT 后 3 个月内作为主要 AFP 更安全、同样有效。