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本文引用的文献

1
10-day decitabine with venetoclax for newly diagnosed intensive chemotherapy ineligible, and relapsed or refractory acute myeloid leukaemia: a single-centre, phase 2 trial.10天阿扎胞苷联合维奈克拉用于新诊断的不适合强化化疗以及复发或难治性急性髓系白血病的治疗:一项单中心2期试验
Lancet Haematol. 2020 Oct;7(10):e724-e736. doi: 10.1016/S2352-3026(20)30210-6. Epub 2020 Sep 5.
2
Azacitidine and Venetoclax in Previously Untreated Acute Myeloid Leukemia.阿扎胞苷和维奈托克治疗未经治急性髓系白血病。
N Engl J Med. 2020 Aug 13;383(7):617-629. doi: 10.1056/NEJMoa2012971.
3
Isavuconazole as Primary Antifungal Prophylaxis in Patients With Acute Myeloid Leukemia or Myelodysplastic Syndrome: An Open-label, Prospective, Phase 2 Study.艾沙康唑作为急性髓系白血病或骨髓增生异常综合征患者的主要抗真菌预防用药:一项开放标签、前瞻性、2期研究。
Clin Infect Dis. 2021 May 18;72(10):1755-1763. doi: 10.1093/cid/ciaa358.
4
Venetoclax plus LDAC for newly diagnosed AML ineligible for intensive chemotherapy: a phase 3 randomized placebo-controlled trial.维奈托克联合 LDAC 方案用于不适合强化化疗的新诊断 AML:一项 3 期随机安慰剂对照试验。
Blood. 2020 Jun 11;135(24):2137-2145. doi: 10.1182/blood.2020004856.
5
Invasive fungal infections in acute myeloid leukemia treated with venetoclax and hypomethylating agents. Venetoclax 联合低甲基化药物治疗急性髓系白血病中的侵袭性真菌感染。
Blood Adv. 2019 Dec 10;3(23):4043-4049. doi: 10.1182/bloodadvances.2019000930.
6
Defining breakthrough invasive fungal infection-Position paper of the mycoses study group education and research consortium and the European Confederation of Medical Mycology.定义突破性侵袭性真菌感染——医学真菌学研究组教育和研究联盟及欧洲医学真菌学会联合会立场文件。
Mycoses. 2019 Sep;62(9):716-729. doi: 10.1111/myc.12960. Epub 2019 Jul 19.
7
Venetoclax Combined With Low-Dose Cytarabine for Previously Untreated Patients With Acute Myeloid Leukemia: Results From a Phase Ib/II Study. Venetoclax 联合低剂量阿糖胞苷治疗未经治疗的急性髓系白血病患者:来自 Ib/II 期研究的结果。
J Clin Oncol. 2019 May 20;37(15):1277-1284. doi: 10.1200/JCO.18.01600. Epub 2019 Mar 20.
8
Treatment with a 5-day versus a 10-day schedule of decitabine in older patients with newly diagnosed acute myeloid leukaemia: a randomised phase 2 trial.新诊断的老年急性髓系白血病患者中,地西他滨5天方案与10天方案治疗的比较:一项随机2期试验
Lancet Haematol. 2019 Jan;6(1):e29-e37. doi: 10.1016/S2352-3026(18)30182-0. Epub 2018 Dec 10.
9
Venetoclax combined with decitabine or azacitidine in treatment-naive, elderly patients with acute myeloid leukemia.维奈托克联合地西他滨或阿扎胞苷治疗初治老年急性髓系白血病患者。
Blood. 2019 Jan 3;133(1):7-17. doi: 10.1182/blood-2018-08-868752. Epub 2018 Oct 25.
10
Antimicrobial Prophylaxis for Adult Patients With Cancer-Related Immunosuppression: ASCO and IDSA Clinical Practice Guideline Update.成人癌症相关免疫抑制患者的抗菌预防:ASCO 和 IDSA 临床实践指南更新。
J Clin Oncol. 2018 Oct 20;36(30):3043-3054. doi: 10.1200/JCO.18.00374. Epub 2018 Sep 4.

伴有 venetoclax 和唑类抗真菌药物的急性髓系白血病患者的细胞减少持续时间。

Duration of cytopenias with concomitant venetoclax and azole antifungals in acute myeloid leukemia.

机构信息

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.

出版信息

Cancer. 2021 Jul 15;127(14):2489-2499. doi: 10.1002/cncr.33508. Epub 2021 Apr 1.

DOI:10.1002/cncr.33508
PMID:33793970
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8249340/
Abstract

BACKGROUND

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.

METHODS

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).

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

方法

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)。

结果

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。

结论

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。

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