Hypomethylating agents plus modified priming regimens compared with venetoclax-based regimens based on molecular characteristics for newly diagnosed patients with acute myeloid leukemia: a multi-center cohort study

被引:2
作者
Weng, Guangyang [1 ]
Huang, Jingya [2 ]
He, Xin [3 ]
Xue, Tingting [1 ]
Yang, Linlin [1 ]
Zhang, Yu [4 ]
Yu, Guopan [4 ]
Sun, Zhiqiang [5 ]
Lin, Dongjun [6 ]
Deng, Lan [7 ]
Liang, Xinquan [8 ]
Xiao, Jie [9 ]
Zhang, Hongyu [10 ]
Guo, Ziwen [3 ]
Jin, Hua [4 ]
Liu, Qifa [4 ]
Du, Xin [1 ]
机构
[1] Shenzhen Univ, Affiliated Hosp 1, Shenzhen Peoples Hosp 2, Dept Hematol, Shenzhen, Peoples R China
[2] Shenzhen Blood Ctr, Shenzhen, Guangdong, Peoples R China
[3] Zhongshan City Peoples Hosp, Dept Hematol, Zhongshan, Peoples R China
[4] Southern Med Univ, Nanfang Hosp, Dept Hematol, Guangzhou, Peoples R China
[5] Southern Med Univ, Shenzhen Hosp, Dept Hematol, Shenzhen, Peoples R China
[6] Sun Yat Sen Univ, Affiliated Hosp 7, Dept Hematol, Shenzhen, Peoples R China
[7] Shanghai Jiao Tong Univ, Sch Med, Shanghai Peoples Hosp 9, Dept Hematol, Shanghai, Peoples R China
[8] First Peoples Hosp Chenzhou, Dept Obstet, Chenzhou, Peoples R China
[9] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Dept Hematol, Guangzhou, Peoples R China
[10] Peking Univ, Shenzhen Hosp, Dept Hematol, Shenzhen, Peoples R China
关键词
Hypomethylating agents; Priming regimens; Venetoclax; Aclarubicin; Homoharringtonine; Acute myeloid leukemia; LOW-DOSE CYTARABINE; COLONY-STIMULATING FACTOR; OLDER PATIENTS; ELDERLY-PATIENTS; G-CSF; AZACITIDINE; DECITABINE; CHEMOTHERAPY; ACLARUBICIN; COMBINATION;
D O I
10.1007/s00277-023-05452-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Venetoclax (VEN)-based regimens are the standard of care for elderly or unfit patients with newly diagnosed (ND) acute myeloid leukemia (AML). Some single-arm studies have implied that hypomethylating agents (HMAs) plus priming regimens may potentially provide an alternative therapeutic approach, owing to encouraging efficacy seen. However, no comparative data exists yet regarding these two treatment approaches. In this retrospective multi-center cohort study, we enrolled 294 ND AML patients, allocating 167 to the HMA + priming group and 127 to the VEN-based group. Treatment response and overall survival (OS) were compared between groups. Molecular subgroup analyses were also conducted. With a median of two cycles for HMA + priming group, the overall response (ORR) was 65.3%, including 55.1% complete remission (CR), 9.6% CR with incomplete hematologic recovery (CRi) and 0.6% morphologic leukemia-free state (MLFS). With a median of two cycles for VEN-based group, the ORR was 70.9%, including 46.5% CR, 18.9% CRi, and 5.5% MLFS. Response differences (ORR or CR/CRi) between groups were not significant (p > 0.05). With a median follow-up of 10.1 months, median OSs were similar between groups (20.9 vs 16.3 months, p = 0.41). However, VEN regimens demonstrated superior CR/CRi for patients with mutations in FLT3, IDH1/2, and NPM1 compared to HMA + priming (80.0% vs 35.0%, p = 0.01; 90.9% vs 65.5%, p = 0.02; 90.9% and 65.5%, p = 0.02, respectively). In conclusion, HMAs plus modified priming regimens might be a potential alternative therapeutic approach for patients with ND AML, but VEN-based regimens presented predominance in specific molecular subgroups. Molecular characteristics contribute to guiding choice of treatment.
引用
收藏
页码:3369 / 3381
页数:13
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