Division of Pharmacy, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cancer. 2021 Jul 15;127(14):2489-2499. doi: 10.1002/cncr.33508. Epub 2021 Apr 1.
Venetoclax (VEN) combined with the hypomethylating agent (HMA) azacitidine improves survival in patients aged ≥75 years with newly diagnosed acute myeloid leukemia (AML). VEN and HMA treatment can result in prolonged and often profound neutropenia, and this warrants antifungal prophylaxis. Azole antifungals inhibit cytochrome P450 3A4, the primary enzyme responsible for VEN metabolism; this results in VEN dose reductions for each concomitant antifungal. Limited clinical data exist on outcomes for patients treated with VEN, an HMA, and various azoles.
The time to neutrophil recovery (absolute neutrophil count [ANC] > 1000 cells/mm ) and platelet (PLT) recovery (PLT count > 100,000 cells/mm ) in 64 patients with newly diagnosed AML who achieved a response after course 1 of VEN plus an HMA were evaluated. HMA therapy included azacitidine (75 mg/m intravenously/subcutaneously for 7 days) or decitabine (20 mg/m intravenously for 5 or 10 days).
Forty-seven patients (73%) received an azole: posaconazole (n = 17; 27%), voriconazole (n = 9; 14%), isavuconazole (n = 20; 31%), or fluconazole (n = 1; 2%). The median time to ANC recovery were similar for patients who did receive an azole (37 days; 95% confidence interval [CI], 34-38 days) and patients who did not receive an azole (39 days; 95% CI, 30 days to not estimable; P = .8). The median time to PLT recovery was significantly longer for patients receiving azoles (28 vs 22 days; P = .01). The median times to ANC recovery (35 vs 38 days) and PLT recovery (26 vs 32 days) were similar with posaconazole and voriconazole.
VEN plus an HMA resulted in neutropenia and thrombocytopenia, with the latter prolonged in patients receiving concomitant azoles. Concomitant posaconazole or voriconazole and VEN (100 mg) resulted in similar ANC and PLT recovery times, suggesting the safety of these dosage combinations during course 1.
维奈托克(VEN)联合低甲基化药物(HMA)阿扎胞苷可改善新诊断为急性髓系白血病(AML)的 75 岁及以上患者的生存。VEN 和 HMA 治疗可导致中性粒细胞减少症延长且常为严重,这需要进行抗真菌预防。唑类抗真菌药抑制细胞色素 P450 3A4,该酶主要负责 VEN 代谢;因此,每伴随使用一种抗真菌药时,都需要降低 VEN 的剂量。目前仅有有限的临床数据可评估接受 VEN、HMA 和各种唑类药物治疗的患者的结局。
评估 64 例新诊断为 AML 的患者在完成 VEN 联合 HMA 一线治疗后达到缓解时的中性粒细胞(绝对中性粒细胞计数 [ANC]>1000 个细胞/mm )和血小板(PLT)恢复(PLT 计数>100000 个细胞/mm )时间。HMA 治疗包括阿扎胞苷(75mg/m 静脉注射/皮下注射,连用 7 天)或地西他滨(20mg/m 静脉注射,连用 5 天或 10 天)。
47 例患者(73%)接受了唑类药物治疗:泊沙康唑(n=17;27%)、伏立康唑(n=9;14%)、伊曲康唑(n=20;31%)或氟康唑(n=1;2%)。接受唑类药物治疗的患者和未接受唑类药物治疗的患者的 ANC 恢复中位时间相似(37 天;95%置信区间 [CI],34-38 天)(P=0.8)。接受唑类药物治疗的患者的 PLT 恢复中位时间明显长于未接受唑类药物治疗的患者(28 天 vs 22 天;P=0.01)。接受泊沙康唑和伏立康唑治疗的患者的 ANC 恢复中位时间(35 天 vs 38 天)和 PLT 恢复中位时间(26 天 vs 32 天)相似。
VEN 联合 HMA 导致中性粒细胞减少和血小板减少,同时接受伴随唑类药物治疗的患者血小板减少更为严重。伴随应用泊沙康唑或伏立康唑和 VEN(100mg)时 ANC 和 PLT 恢复时间相似,提示在第 1 疗程期间这些剂量组合是安全的。