Service d'Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse-Oncopole, Toulouse, France.
Centre Hospitalier Universitaire de Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire, Bordeaux, France.
Leuk Lymphoma. 2022 Jun;63(6):1398-1406. doi: 10.1080/10428194.2021.2022140. Epub 2022 Jan 4.
We analyzed 526 consecutive acute myeloid leukemia patients refractory to or relapsing after chemotherapy. 270 patients received intensive salvage chemotherapy (IC), 97 azacitidine (AZA) and 159 best supportive care (BSC). Complete response was obtained in 37/19/0% ( = .0008). Allogeneic stem-cell transplantation (alloSCT) was performed in 39.3/10.3/0%. Median overall survival (OS) and 5-year OS were 8.2/9.6/2.2 months and 16/6/2% ( < .0001). Predictive factors of worse OS were post-myelodysplastic/chronic myelomonocytic leukemia, bone marrow blasts ≥20%, adverse cytogenetics, AZA cycle ≥2 and no alloSCT at R/R for AZA and age, performance status, white blood cell count and myelodysplasia-related changes for IC. The impact of treatment was time-dependent: adjusted hazard ratio for OS was in favor of AZA up to 1 month, was not different between 1 and 7 months, then was in favor of IC after 7 months. While AZA represents a therapeutic option for the oldest patients, it does not lead to long-term survivors.
我们分析了 526 例对化疗耐药或复发的急性髓系白血病患者。270 例患者接受强化挽救化疗(IC),97 例接受阿扎胞苷(AZA)治疗,159 例接受最佳支持治疗(BSC)。完全缓解率分别为 37/19/0%( = .0008)。39.3/10.3/0%的患者接受了异基因造血干细胞移植(alloSCT)。中位总生存期(OS)和 5 年 OS 分别为 8.2/9.6/2.2 个月和 16/6/2%( < .0001)。OS 更差的预测因素包括 MDS/CMML 后、骨髓原始细胞≥20%、不良细胞遗传学、AZA 周期≥2 个和 R/R 时未接受 alloSCT 以及 AZA 时的年龄、表现状态、白细胞计数和 MDS 相关改变,IC 时为年龄、表现状态、白细胞计数和 MDS 相关改变。治疗的影响是时间依赖性的:OS 的调整后危险比有利于 AZA 至 1 个月,1 至 7 个月之间无差异,7 个月后有利于 IC。虽然 AZA 是老年患者的一种治疗选择,但它不能带来长期生存。