Wang Bin-Ru, Wan Chao-Ling, Liu Song-Bai, Qiu Qiao-Cheng, Wu Tian-Mei, Wang Jun, Li Yan-Yan, Ge Shuai-Shuai, Qiu Yan, Shen Xiang-Dong, Xue Sheng-Li, Li Zheng
National Clinical Research Center for Hematologic Diseases, Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, China.
Institute of Blood and Marrow Transplantation, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, China.
Front Oncol. 2021 Dec 9;11:797941. doi: 10.3389/fonc.2021.797941. eCollection 2021.
The management of patients with relapsed or refractory (R/R) acute myeloid leukaemia (AML) remains a challenge with few reliably effective treatments. Chidamide, a new selective HDAC inhibitor, has demonstrated some effectiveness in AML patients. Herein, we reported three patients with R/R AML who were unresponsive to venetoclax plus azacitidine (VA) but were successfully treated with VA when chidamide was added to the regimen. MCL1 is one of the anti-apoptotic proteins. Chidamide targets the MCL1 protein, which may permit venetoclax resistance when upregulated. We determined MCL1 protein expression in different AML cell lines, and chidamide could downregulate MCL1 expression in venetoclax resistance AML cells. In general, our experience showed that the chidamide/VA combination could improve the condition of R/R AML patients who are resistant to VA. Formally evaluating this regimen in R/R AML patients may be meaningful.
复发或难治性(R/R)急性髓系白血病(AML)患者的管理仍然是一项挑战,可靠有效的治疗方法很少。西达本胺是一种新型选择性组蛋白去乙酰化酶(HDAC)抑制剂,已在AML患者中显示出一定疗效。在此,我们报告了3例R/R AML患者,他们对维奈克拉联合阿扎胞苷(VA)无反应,但在该方案中加入西达本胺后成功接受了VA治疗。髓细胞白血病-1(MCL1)是一种抗凋亡蛋白。西达本胺靶向MCL1蛋白,当MCL1蛋白上调时可能导致对维奈克拉耐药。我们测定了不同AML细胞系中MCL1蛋白的表达,西达本胺可下调维奈克拉耐药AML细胞中MCL1的表达。总体而言,我们的经验表明,西达本胺/VA联合方案可改善对VA耐药的R/R AML患者的病情。在R/R AML患者中对该方案进行正式评估可能具有意义。