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停止基于 venetoclax 的治疗后急性髓系白血病患者的无治疗缓解。

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

机构信息

The Alfred Hospital and Monash University, Melbourne, Australia.

The Walter and Eliza Hall Institute of Medical Research, Parkville, Melbourne, Australia.

出版信息

Blood Adv. 2022 Jul 12;6(13):3879-3883. doi: 10.1182/bloodadvances.2022007083.

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.

摘要

在新诊断的老年和/或不适合接受治疗的急性髓系白血病(AML)患者中,联合 venetoclax(VEN)与低剂量阿糖胞苷或低甲基化药物治疗可带来临床获益,这已在 3 期研究中得到证实。随着基于 VEN 的治疗方案在 AML 患者中的应用增加,一个相关问题是对于已达到持续缓解的患者,是否可以安全地停止治疗。我们假设,一部分选择停止治疗的患者可能会从无治疗缓解(TFR)期获益,而无需无限期治疗。我们报告了 29 例患者的回顾性结果,这些患者在接受基于 VEN 的治疗后缓解至少 12 个月,其中 55%的患者继续治疗直至疾病进展,45%的患者选择性停止治疗(STOP)。随访时间超过 5 年,我们观察到 STOP 队列中有 45.8 个月的中位 TFR,数据截止时仍有>50%的患者处于持续缓解状态。两组患者的复发风险、无复发生存期和总生存期相似。在该队列中,有利于持续 TFR 的因素包括诊断时存在 NPM1 和/或 IDH2 突变、无微小残留病的完全缓解,以及在停止治疗前至少接受 12 个月的基于 VEN 的联合治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc43/9278306/c9dfd026f815/advancesADV2022007083f1.jpg

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