Efficacy of Azacitidine Plus Venetoclax in Acute Myeloid Leukemia Transformed from Myelodysplastic Syndrome after Failure of Azacitidine Monotherapy.

Takafumi Furumoto, Koji Ando, Eo Toriyama, Tomoko Hata, Shinichi Katsuoka, Saori Nishimura, Masamitsu Ichinose, Miki Hashimoto, Machiko Fujioka, Chika Sakaki, Hikaru Sakamoto, Masahiko Chiwata, Rena Kamijo, Yuji Kobayashi, Hideaki Kitanosono, Jun Nakashima, Takeharu Kato, Masataka Taguchi, Makiko Horai, Masatoshi Matsuo, Junya Makiyama, Hidehiro Itonaga, Shinya Sato, Maki Baba, Yasushi Sawayama, Yumi Takasaki, Jun Taguchi, Daisuke Imanishi, Yoshitaka Imaizumi, Yasuhisa Kawaguchi, Hideki Tsushima, Tatsuro Jo, Shinichiro Yoshida, Yukiyoshi Moriuchi, Yasushi Miyazaki
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Abstract

Objective Patients with acute myeloid leukemia (AML) transformed from myelodysplastic syndrome (MDS) have a poor prognosis, including those treated with azacitidine during the MDS phase; there is no standard for the care of these patients. Recently, azacitidine plus venetoclax (AZA/VEN) was reported to prolong the survival in treatment-naïve AML patients compared with AZA monotherapy. However, the results of AZA/VEN for AML transformed from MDS, particularly after AZA monotherapy, remain unclear. The present study therefore compared the clinical results of AZA/VEN treatment in these patients. Methods and Patients Data from MDS patients diagnosed at 10 institutions in Nagasaki Prefecture were collected. Thereafter, patients with transformed AML following AZA monotherapy during the MDS phase were selected, and their treatment response and survival were analyzed. Results The overall response (OR) rate, overall survival (OS), and event-free survival (EFS) were compared among patients treated with AZA/VEN (n=13), chemotherapy (intensive and low-intensity, n=35), AZA monotherapy (mAZA, n=15), and best supportive care (BSC, n=43) after AML transformation. The corresponding OR rates were 38.5%, 20.0%, and 6.7% for the AZA/VEN, chemotherapy, and mAZA groups, respectively (p=0.235). The respective median OS and EFS were 10.7 and 8.9 months for AZA/VEN, 3.2 and 2.0 months for chemotherapy, and 3.8 and 2.7 months for mAZA, and 1.7 months for BSC (OS only) (p=0.000023 for the OS and p=0.026 for the EFS), Conclusion Our findings suggest the superiority of AZA/VEN for AML patients with transformation from MDS following AZA monotherapy.

阿扎胞苷联合Venetoclax治疗阿扎胞苷单药治疗失败后由骨髓增生异常综合征转化的急性髓系白血病疗效观察。
目的骨髓增生异常综合征(MDS)转化为急性髓性白血病(AML)的患者预后较差,包括在MDS期接受阿扎胞苷治疗的患者;对这些病人的护理没有标准。最近,阿扎胞苷加venetoclax (AZA/VEN)与AZA单药治疗相比可延长treatment-naïve AML患者的生存期。然而,AZA/VEN治疗MDS转化的AML的结果,特别是在AZA单药治疗后,仍不清楚。因此,本研究比较了AZA/VEN治疗这些患者的临床结果。方法收集长崎县10家医疗机构诊断的MDS患者资料。随后,选择MDS期接受AZA单药治疗的转化性AML患者,分析其治疗反应和生存期。结果比较了AML转化后接受AZA/VEN (n=13)、化疗(强化和低强度,n=35)、AZA单药治疗(mAZA, n=15)和最佳支持治疗(BSC, n=43)的患者的总缓解率(OR)、总生存期(OS)和无事件生存期(EFS)。AZA/VEN组、化疗组和mAZA组相应的OR率分别为38.5%、20.0%和6.7% (p=0.235)。AZA/VEN组的中位OS和EFS分别为10.7和8.9个月,化疗组为3.2和2.0个月,mAZA组为3.8和2.7个月,BSC组为1.7个月(仅OS) (OS为p=0.000023, EFS为p=0.026)。结论:AZA/VEN对AZA单药治疗后MDS转化的AML患者具有优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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