Liu Pengpeng, Hang Xiaohang, Li Jianjun, Zhao Lei, Liu Weiping, Ji Jie, Wu Yu, Wan Xudong, Shuai Xiao, Guo Yong, Xiang Bing, Liu Jiazhuo, Huang Jie, Liu Zhigang, Hou Li, Chen Chong, Liu Yu, Liu Ting
Department of Hematology, Institute of Hematology, West China Hospital, Sichuan University Chengdu 610041, Sichuan, China.
State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University Chengdu 610041, Sichuan, China.
Am J Cancer Res. 2024 Jun 15;14(6):2921-2933. doi: 10.62347/GIIR3351. eCollection 2024.
Double expressor lymphoma (DEL), characterized by high expressions of both MYC and BCL-2, displays poor prognosis after current therapies. The HDAC inhibitor chidamide has been approved for treatment of T cell lymphoma, but its efficacy on B cell lymphoma is unclear. Here, by combining inhibition screening and transcriptomic analyses, we found that the sensitivity of B lymphoma cells to chidamide was positively correlated with the expression levels of MYC. Chidamide treatment reduced MYC protein levels and repressed MYC pathway in B lymphoma cells with high MYC expressions. Ectopic expression of MYC in chidamide-insensitive B lymphoma cells increased their response to chidamide. Thus, we proposed that adding chidamide into R-CHOP (CR-CHOP) might be effective for DEL, and retrospectively analyzed 185 DEL patients treated in West China Hospital. 80% of patients showed response to CR-CHOP treatment. In the median follow-up of 42 months, CR-CHOP significantly improve the survival for DEL patients with R-IPI ≤2. Totally 35 patients underwent autologous stem cell transplantation (ASCT) in remission and demonstrated a trend for better survival. Combining CR-CHOP with ASCT resulted in the most superior PFS and OS above all. For response patients, CR-CHOP reduced relapse with better PFS than R-CHOP-like regimens with or without ASCT. Taken together, our data indicated that chidamide repressed the MYC pathway in B lymphoma and is potentially efficacious to treat DEL.
双表达淋巴瘤(DEL)以MYC和BCL-2的高表达为特征,在当前治疗后预后较差。组蛋白去乙酰化酶抑制剂西达本胺已被批准用于治疗T细胞淋巴瘤,但其对B细胞淋巴瘤的疗效尚不清楚。在这里,通过结合抑制筛选和转录组分析,我们发现B淋巴瘤细胞对西达本胺的敏感性与MYC的表达水平呈正相关。西达本胺治疗降低了高MYC表达的B淋巴瘤细胞中MYC蛋白水平并抑制了MYC通路。在对西达本胺不敏感的B淋巴瘤细胞中异位表达MYC增加了它们对西达本胺的反应。因此,我们提出在R-CHOP(CR-CHOP)方案中加入西达本胺可能对DEL有效,并对在华西医院治疗的185例DEL患者进行了回顾性分析。80%的患者对CR-CHOP治疗有反应。在42个月的中位随访中,CR-CHOP显著提高了R-IPI≤2的DEL患者的生存率。共有35例患者在缓解期接受了自体干细胞移植(ASCT),并显示出更好的生存趋势。将CR-CHOP与ASCT联合使用导致了最优越的无进展生存期(PFS)和总生存期(OS)。对于有反应的患者,CR-CHOP比有或没有ASCT的R-CHOP样方案降低了复发率,PFS更好。综上所述,我们的数据表明西达本胺抑制了B淋巴瘤中的MYC通路,对治疗DEL可能有效。