Suppr超能文献

一种成功的桥接疗法:将去甲基化药物与维奈克拉联合用于新诊断或复发/难治性急性髓系白血病成年患者

A Successful Bridge Therapy Combining Hypomethylating Agents with Venetoclax for Adult Patients with Newly Diagnosed or Relapsed/Refractory Acute Myeloid Leukemia.

作者信息

Bang Su-Yeon, Park Silvia, Kwag Daehun, Lee Jong Hyuk, Min Gi-June, Park Sung-Soo, Yoon Jae-Ho, Lee Sung-Eun, Cho Byung-Sik, Eom Ki-Seong, Kim Yoo-Jin, Lee Seok, Min Chang-Ki, Cho Seok-Goo, Lee Jong Wook, Kim Hee-Je

机构信息

Department of Hematology, Catholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.

Leukemia Research Institute, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.

出版信息

Cancers (Basel). 2023 Mar 8;15(6):1666. doi: 10.3390/cancers15061666.

Abstract

Recently, the combination of VEN-HMA has been shown to achieve durable responses in patients with both newly diagnosed (ND) and R/R-AML. We retrospectively evaluated the post-allo-HCT outcomes of 50 patients who received VEN-HMA therapy. In total, 10 were ND and 40 were R/R and, at the time of HCT, the median age was 53 years. In the ND- and R/R-AML groups, the percentage of patients who achieved CR/CRi or MLFS was 90% and 92.5%, respectively. In all, after a median follow-up of 13.7 months, the probabilities of overall survival (OS), relapse-free survival (RFS), cumulative incidence of relapse (CIR), and nonrelapse mortality (NRM) at 1 year were 63.7%, 59.3%, 28.5%, and 12.2%, respectively. In addition, the cumulative incidences of grade II-IV acute graft-versus-host disease (GVHD) and moderate-severe chronic GVHD at 1 year were 28.4% and 37.4%, respectively. In multivariate analysis, the factors associated with a statistically significant impact on OS were VEN-HMA cycle ( = 0.021), ELN risk group ( = 0.041), and the response to VEN-HMA therapy before allo-HCT ( = 0.003). Although 80% of our patients had R/R-AML and 30% underwent a second allo-HCT, our data still suggest that allo-HCT following VEN-HMA therapy is a safe and effective treatment option.

摘要

最近,VEN-HMA联合疗法已被证明可使新诊断(ND)和复发/难治性急性髓系白血病(R/R-AML)患者获得持久缓解。我们回顾性评估了50例接受VEN-HMA治疗的患者异基因造血干细胞移植(allo-HCT)后的结局。总共有10例为ND患者,40例为R/R患者,造血干细胞移植时的中位年龄为53岁。在ND-AML组和R/R-AML组中,达到完全缓解/完全缓解伴血细胞计数未完全恢复(CR/CRi)或微小残留病灶阴性(MLFS)的患者比例分别为90%和92.5%。总体而言,在中位随访13.7个月后,1年时的总生存(OS)概率、无复发生存(RFS)概率、累积复发率(CIR)和非复发死亡率(NRM)分别为63.7%、59.3%、28.5%和12.2%。此外,1年时II-IV级急性移植物抗宿主病(GVHD)和中重度慢性GVHD的累积发生率分别为28.4%和37.4%。在多变量分析中,对OS有统计学显著影响的因素为VEN-HMA疗程(P = 0.021)、欧洲白血病网络(ELN)风险组(P = 0.041)以及allo-HCT前对VEN-HMA治疗的反应(P = 0.003)。尽管我们80%的患者为R/R-AML,30%的患者接受了第二次allo-HCT,但我们的数据仍表明VEN-HMA治疗后进行allo-HCT是一种安全有效的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d092/10046472/b1710318d25b/cancers-15-01666-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验