Department of Hematologic Oncology, National Hospital Organization Shikoku Cancer Center, Matsuyama, Japan.
Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Mycoses. 2020 Aug;63(8):794-801. doi: 10.1111/myc.13100. Epub 2020 May 28.
Fungal infections are a major complication of neutropaenia following chemotherapy. Their early diagnosis is difficult, and empirical antifungal treatment is widely used, and uses of less toxic drugs that reduce breakthrough infection are required.
We conducted a multicentre, open-label, randomised, non-inferiority trial to compare the safety and efficacy of intravenous itraconazole (ivITCZ) and liposomal amphotericin B (LAmB) as empirical antifungal therapy in patients with haematological malignancies with neutropaenia and persistent fever.
Patients with haematological malignancies who developed fever refractory to broad-spectrum antibacterial agents under neutropaenia conditions were enrolled. Patients were randomised for treatment with LAmB (3.0 mg/kg/d) or ivITCZ (induction: 400 mg/d, maintenance: 200 mg/d).
Observed overall favourable response rates of 17/52 (32.7%) and 18/50 (36.0%) in the LAmB and ivITCZ groups, with a model-based estimate of a 4% difference (90% CI, -12% to 20%), did not fulfil the statistical non-inferiority criterion. In the LAmB group, there were two cases of breakthrough infection and five cases of probable invasive fungal disease, whereas in the itraconazole group, neither breakthrough infection nor probable invasive fungal disease occurred. Patients in the ivITCZ group had significantly fewer grade 3-4 hypokalaemia-related events than LAmB group patients (P < .01). The overall incidence of adverse events tended to be lower in the ivITCZ group (P = .07).
ivITCZ showed similar efficacy and safety as LAmB as empirical antifungal therapy in haematological malignancy patients with febrile neutropaenia, although the small sample size and various limitations prevented demonstration of its non-inferiority.
真菌感染是化疗后中性粒细胞减少的主要并发症。早期诊断困难,广泛使用经验性抗真菌治疗,需要使用毒性较小的药物来减少突破性感染。
我们进行了一项多中心、开放标签、随机、非劣效性试验,比较静脉注射伊曲康唑(ivITCZ)和脂质体两性霉素 B(LAmB)作为中性粒细胞减少和持续性发热的血液恶性肿瘤患者经验性抗真菌治疗的安全性和疗效。
纳入血液恶性肿瘤患者,在中性粒细胞减少条件下发热对广谱抗菌药物耐药。患者随机接受 LAmB(3.0mg/kg/d)或 ivITCZ(诱导:400mg/d,维持:200mg/d)治疗。
观察到 LAmB 组和 ivITCZ 组的总有效反应率分别为 17/52(32.7%)和 18/50(36.0%),模型估计差异为 4%(90%CI,-12%至 20%),未满足统计学非劣效性标准。LAmB 组有 2 例突破感染和 5 例可能侵袭性真菌感染,而 ivITCZ 组均未发生突破感染和可能侵袭性真菌感染。ivITCZ 组低钾血症相关 3-4 级不良事件发生率明显低于 LAmB 组(P<.01)。ivITCZ 组不良事件总发生率较低(P=0.07)。
ivITCZ 作为血液恶性肿瘤发热性中性粒细胞减少患者的经验性抗真菌治疗,与 LAmB 具有相似的疗效和安全性,尽管样本量小且存在各种局限性,无法证明其非劣效性。