Treatment-free remission after ceasing venetoclax-based therapy in patients with acute myeloid leukemia

被引:46
作者
Chua, Chong Chyn [1 ,2 ,3 ,4 ]
Hammond, Danielle [5 ]
Kent, Andrew [6 ]
Tiong, Ing Soo [1 ,2 ,7 ]
Konopleva, Marina Y. [5 ]
Pollyea, Daniel A. [6 ]
DiNardo, Courtney D. [5 ]
Wei, Andrew H. [1 ,2 ,3 ,8 ,9 ,10 ,11 ]
机构
[1] Alfred Hosp, Melbourne, Australia
[2] Monash Univ, Melbourne, Australia
[3] Walter & Eliza Hall Inst Med Res, Melbourne, Australia
[4] Northern Hosp, Dept Clin Haematol, Melbourne, Australia
[5] Univ Texas MD Anderson Canc Ctr, Houston, TX USA
[6] Univ Colorado, Div Hematol, Sch Med, Aurora, CO USA
[7] Peter MacCallum Canc Ctr, Dept Pathol, Melbourne, Australia
[8] Royal Melbourne Hosp, Peter MacCallum Canc Ctr, Melbourne, Australia
[9] Univ Melbourne, Melbourne, Australia
[10] Peter MacCallum Canc Ctr, 305 Grattan St, Melbourne, VIC 3000, Australia
[11] Royal Melbourne Hosp, 305 Grattan St, Melbourne, VIC 3000, Australia
基金
英国医学研究理事会;
关键词
AZACITIDINE;
D O I
10.1182/bloodadvances.2022007083
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The clinical benefit of adding venetoclax (VEN) to hypomethylating agents or low-dose cytarabine in older and/or unfit patients with newly diagnosed acute myeloid leukemia (AML) has been confirmed in phase 3 studies. With the increased uptake of VEN-based therapies for patients with AML, a pertinent question is whether treatment can be safely ceased among patients who have achieved sustained remission. We hypothesized that a proportion of patients opting to cease therapy may benefit from a treatment-free remission (TFR) period without indefinite treatment. We report the retrospective outcomes of 29 patients in remission for a minimum of 12 months on VEN-based therapy, with 55% continuing therapy until disease progression and 45% electively ceasing treatment (STOP). With follow-up exceeding 5 years, we observed a median TFR lasting 45.8 months among the STOP cohort, with .50% of patients still in sustained remission at the data cutoff. The risk of relapse and duration of relapse-free and overall survival were similar between the 2 cohorts. Factors favoring sustained TFR within the cohort included NPM1 and/or IDH2 mutation at diagnosis, complete remission without measurable residual disease, and at least 12 months of VEN-based combination therapy prior to treatment cessation.
引用
收藏
页码:3879 / 3883
页数:5
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