Outcomes Are Similar After Allogeneic Hematopoietic Stem Cell Transplant for Newly Diagnosed Acute Myeloid Leukemia Patients who Received Venetoclax + Azacitidine Versus Intensive Chemotherapy

医学 威尼斯人 内科学 肿瘤科 累积发病率 阿扎胞苷 移植 髓系白血病 危险系数 造血干细胞移植 挽救疗法 单变量分析 白血病 化疗 多元分析 慢性淋巴细胞白血病 置信区间 生物化学 基因表达 化学 DNA甲基化 基因
作者
Amanda Winters,Grace Bosma,Daniel A. Pollyea,Mohammad Minhajuddin,Craig T. Jordan,Daniel A. Pollyea,Jonathan A. Gutman
标识
DOI:10.1016/j.jtct.2022.07.022
摘要

Allogeneic hematopoietic stem cell transplantation (SCT) after a patient with acute myeloid leukemia (AML) achieves a remission from intensive chemotherapy (IC) is given with curative intent. Recently, venetoclax-based regimens have become the standard of care for patients with newly diagnosed AML who are unfit for IC. If these patients achieve remission, they may also be considered for potentially curative consolidation with SCT. There are limited data comparing outcomes after SCT with these different induction strategies. The purpose of the current study was to evaluate depth of remission before SCT and outcomes after SCT in adults with nonrelapsed/refractory AML receiving pre-SCT therapy with either venetoclax/azacitidine (ven/aza) or IC. This was a retrospective, single-institution analysis of 169 patients receiving SCT in first remission after IC or ven/aza. Patient demographics and AML risk features were collected, as well as pre-SCT measurable residual disease (MRD) assessed by flow cytometry and molecular methods. Relapse, transplantation-related mortality, incidence of acute and chronic graft-versus-host-disease (GVHD), and death from any cause were also recorded. Descriptive and survival statistics were applied to these data to compare IC and ven/aza groups. Cox proportional hazard models were used for univariate and multivariate analyses. We demonstrate that despite differences in baseline factors between these groups, outcomes were similar. Relapse-free and overall survival, as well as cumulative incidences of transplantation-related mortality, relapse, and acute and chronic GVHD were comparable between groups. Exploring survival in younger (<65 years) versus older (≥65 years) patients by treatment group did not alter these results. Finally, although pre-SCT MRD by flow cytometry was significantly predictive of post-SCT relapse and survival in the IC + SCT patients, it was not significantly predictive of relapse and survival in the ven/aza + SCT patients. Although these findings require prospective validation in a larger cohort of patients, they suggest that ven/aza followed by SCT is a reasonable management strategy for transplantation candidates at any age.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
领导范儿应助王焕玉采纳,获得10
刚刚
袁融发布了新的文献求助10
刚刚
1秒前
彭于晏应助酷炫采珊采纳,获得10
1秒前
hao完成签到,获得积分10
2秒前
啦啦完成签到,获得积分10
2秒前
放空的酸奶完成签到,获得积分10
3秒前
rjx完成签到,获得积分10
4秒前
4秒前
整齐芷文完成签到,获得积分10
4秒前
小恩发布了新的文献求助10
5秒前
6秒前
7秒前
rjx发布了新的文献求助10
7秒前
无花果应助於无血采纳,获得10
7秒前
7秒前
8秒前
HQQ完成签到,获得积分10
9秒前
10秒前
10秒前
二九十二完成签到,获得积分10
10秒前
morena发布了新的文献求助10
10秒前
小罗萝卜发布了新的文献求助30
10秒前
11秒前
11秒前
Wang发布了新的文献求助10
11秒前
大个应助登峰采纳,获得10
12秒前
香蕉觅云应助美好不愁采纳,获得10
14秒前
14秒前
14秒前
LYKKE完成签到,获得积分20
15秒前
好香芋泥煎意面完成签到 ,获得积分10
16秒前
子车采蓝发布了新的文献求助10
17秒前
17秒前
18秒前
123发布了新的文献求助10
18秒前
星辰大海应助傻傻的不评采纳,获得10
18秒前
nenoaowu发布了新的文献求助10
19秒前
科研通AI6.2应助袁融采纳,获得30
19秒前
DrLin完成签到,获得积分10
20秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Developing Genetic Editing Tools for Lysobacter 2000
Моделирование процессов самоорганизации в кристаллообразующих системах 1000
Adhesion Science: Principles & Practice 800
Signals, Systems, and Signal Processing 610
IEST-RP-CC018: Cleanroom Cleaning and Sanitization: Operating and Monitoring Procedures 600
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 600
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6528290
求助须知:如何正确求助?哪些是违规求助? 8321388
关于积分的说明 17814026
捐赠科研通 5629979
什么是DOI,文献DOI怎么找? 2930705
邀请新用户注册赠送积分活动 1907434
关于科研通互助平台的介绍 1766795