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阿扎胞苷联合维奈克拉治疗复发和新诊断的急性髓系白血病患者

Azacitidine Plus Venetoclax for the Treatment of Relapsed and Newly Diagnosed Acute Myeloid Leukemia Patients.

作者信息

Garciaz Sylvain, Hospital Marie-Anne, Alary Anne-Sophie, Saillard Colombe, Hicheri Yosr, Mohty Bilal, Rey Jérôme, D'Incan Evelyne, Charbonnier Aude, Villetard Ferdinand, Maisano Valerio, Lombardi Laura, Ittel Antoine, Mozziconacci Marie-Joelle, Gelsi-Boyer Véronique, Vey Norbert

机构信息

INSERM, CNRS, Department of Hematology, Institut Paoli-Calmettes, Aix-Marseille University, 13009 Marseille, France.

Deparment of Hematology, Institut Paoli-Calmettes, 13009 Marseille, France.

出版信息

Cancers (Basel). 2022 Apr 16;14(8):2025. doi: 10.3390/cancers14082025.

Abstract

Venetoclax (VEN) belongs the BH3-mimetic class that selectively targets BCL-2, activating apoptosis. The combination of VEN and azacitidine (AZA) has changed the paradigm of treatment of newly diagnosed (ND) acute myeloid leukemia (AML) patients ineligible for intensive chemotherapy. There is scarce evidence for the use of VEN-AZA for relapsed or refractory (R/R) AML. We compared the outcome of 39 R/R AML and 38 ND AML patients treated between 01/20 and 12/21. The median age was 69 (22-86) and 73 (61-81) in the R/R and ND groups, respectively. Adverse cytogenetics were found in 36% of patients in the R/R group and 59% of patients in the ND group. Overall response rate was 37% in R/R AML, including 13% CR, 8% CRi, 3% PR and 13% MLFS, and 58% in the ND AML, including 32% CR, 13% CRi and 13% MLFS. Adverse cytogenetics was associated with treatment failure in the R/R group (Relative Risk = 0.13, = 0.005). Median overall survival (OS) was 5.9 months in the R/R group and 9.4 months in the ND group. Median OS was 2.2 months in the adverse cytogenetics group versus 8.7 months in the intermediate cytogenetics group in the R/R group ( = 0.02). Median leukemia-free survival was not different between the two groups (9.4 months and 10.3 months), indicating that VEN-AZA can be an efficient salvage treatment for selected R/R AML patients. In conclusion, VEN-AZA is a promising treatment for ND AML and for selected R/R AML patients.

摘要

维奈克拉(VEN)属于BH3模拟物类别,可选择性靶向BCL-2,激活细胞凋亡。VEN与阿扎胞苷(AZA)联合使用改变了新诊断(ND)的不适合强化化疗的急性髓系白血病(AML)患者的治疗模式。关于VEN-AZA用于复发或难治性(R/R)AML的证据很少。我们比较了20年1月至21年12月期间治疗的39例R/R AML患者和38例ND AML患者的结局。R/R组和ND组的中位年龄分别为69岁(22-86岁)和73岁(61-81岁)。R/R组36%的患者和ND组59%的患者存在不良细胞遗传学特征。R/R AML的总缓解率为37%,包括13%的完全缓解(CR)、8%的部分缓解伴血细胞计数未完全恢复(CRi)、3%的部分缓解(PR)和13%的微小血液学缓解(MLFS);ND AML的总缓解率为58%,包括32%的CR、13%的CRi和13%的MLFS。不良细胞遗传学特征与R/R组的治疗失败相关(相对风险=0.13,P=0.005)。R/R组的中位总生存期(OS)为5.9个月,ND组为9.4个月。R/R组中不良细胞遗传学组的中位OS为2.2个月,而中等细胞遗传学组为8.7个月(P=0.02)。两组的无白血病生存期中位数无差异(分别为9.4个月和10.3个月),这表明VEN-AZA可以作为部分R/R AML患者的有效挽救治疗方法。总之,VEN-AZA对于ND AML和部分R/R AML患者是一种有前景的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a265/9028084/6fa65a7a1833/cancers-14-02025-g001.jpg

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