医学
威尼斯人
文
阿扎胞苷
内科学
髓系白血病
挽救疗法
中性粒细胞减少症
发热性中性粒细胞减少症
耐火材料(行星科学)
急性白血病
感染性休克
肿瘤科
白血病
胃肠病学
败血症
化疗
慢性淋巴细胞白血病
化学
DNA甲基化
基因表达
物理
基因
天体生物学
生物化学
计算机科学
计算机安全
作者
Andrée-Anne Pelland,Xavier Deschênes‐Simard,Xavier Savard,Philippe Giguère,David Spillane,Frédéric Barabé,Vinçent Laroche,Michaël Munger,Geneviève Gallagher,Nicolas Marcoux,Guy Cantin,Maxime Chénard-Poirier,Robert Delage,Marc Lalancette,Olivier Veilleux,Sarit Assouline,Christopher Lemieux
标识
DOI:10.1080/10428194.2024.2390574
摘要
This study reports characteristics and outcomes of adults who received Azacitidine-Venetoclax (AZA-VEN) compared to other salvage therapies (NO-AZA-VEN) as first salvage therapy for acute myeloid leukemia (AML). The clinical data of 81 patients with a diagnosis of relapsed or refractory AML were analyzed. The ORR was comparable for both groups (55% vs 57%, p = 0.852). Median OS (6.8 vs 11.2 months, p = 0.053) and median RFS (6.9 vs 11.2 months, p = 0.488) showed a trend in favor of the NO-AZA-VEN group. OS was significantly longer with NO-AZA-VEN for ELN 2022 risk category sub-group, patients under 60 years old, primary AML and for patients who underwent allo-hematopoietic stem cell transplant after salvage therapy. There was no statistical difference in complications of treatment such as febrile neutropenia, intensive care unit stay, septic shock and total parenteral nutrition. Those results do not support the preferential use of AZA-VEN over other regimens in R/R acute myeloid leukemia.
科研通智能强力驱动
Strongly Powered by AbleSci AI