威尼斯人
医学
阿糖胞苷
内科学
髓系白血病
队列
氟达拉滨
完全缓解
微小残留病
肿瘤科
环磷酰胺
养生
白血病
儿科
化疗
慢性淋巴细胞白血病
作者
Chong Chyn Chua,Danielle Hammond,Andrew Kent,Ing Soo Tiong,Marina Konopleva,Daniel A. Pollyea,Courtney D. DiNardo,Andrew H. Wei
出处
期刊:Blood Advances
[Elsevier BV]
日期:2022-05-05
卷期号:6 (13): 3879-3883
被引量:56
标识
DOI:10.1182/bloodadvances.2022007083
摘要
Abstract 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.
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