Medical Clinic and Policlinic I, Hematology and Cellular Therapy, University Hospital Leipzig, Leipzig, Germany.
German Cancer Research Center (DKFZ), Heidelberg, Germany.
Leukemia. 2020 Sep;34(9):2333-2341. doi: 10.1038/s41375-020-0758-4. Epub 2020 Feb 19.
Data on outcome in older (≥70 years) patients with acute promyelocytic leukemia after treatment with arsenic trioxide (ATO) compared with standard chemotherapy (CTX) is scarce. We evaluated 433 patients (median age, 73.4 years) treated either with ATO+ all-trans retinoic acid (ATO/ATRA; n = 26), CTX/ATRA + ATO during consolidation (CTX/ATRA/ATO; n = 148), or with CTX/ATRA (n = 259). Median follow-up for overall survival (OS) was 4.8 years. Complete remissions (CR) were achieved in 92% with ATO/ATRA and 82% with CTX/ATRA; induction death rates were 8% and 18%, respectively. For analysis of postremission outcomes we combined the ATO/ATRA and CTX/ATRA/ATO groups (ATO/ATRA ± CTX). Cumulative incidence of relapse (CIR) was significantly lower after ATO/ATRA ± CTX compared with CTX/ATRA (P < 0.001). The same held true when restricting the analysis according to the treatment period after the year 2000. OS of patients in CR1 was not different between ATO/ATRA ± CTX compared with CTX/ATRA (P = 0.20). High (>10 × 10/l) white blood cell (WBC) counts at diagnosis were associated with higher CIR (P < 0.001) compared with lower WBC in the CTX/ATRA group, but not in the ATO/ATRA ± CTX group (P = 0.48). ATO, when added to ATRA or CTX/ATRA is feasible and effective in elderly patients for remission induction and consolidation, particularly in patients with high WBC at diagnosis.
在接受三氧化二砷(ATO)治疗的老年(≥70 岁)急性早幼粒细胞白血病患者与接受标准化疗(CTX)的患者相比,其治疗结果的数据较为匮乏。我们评估了 433 名患者(中位年龄 73.4 岁),他们分别接受 ATO+全反式维甲酸(ATO/ATRA;n=26)、CTX/ATRA+ATO 巩固治疗(CTX/ATRA/ATO;n=148)或 CTX/ATRA(n=259)治疗。中位总生存(OS)随访时间为 4.8 年。ATO/ATRA 组完全缓解率(CR)为 92%,CTX/ATRA/ATO 组为 82%;诱导死亡率分别为 8%和 18%。为了分析缓解后结局,我们将 ATO/ATRA 和 CTX/ATRA/ATO 组(ATO/ATRA±CTX)进行了合并。与 CTX/ATRA 组相比,ATO/ATRA±CTX 组的复发累积发生率(CIR)显著降低(P<0.001)。当根据 2000 年后的治疗期限制分析时,同样如此。ATO/ATRA±CTX 组 CR1 患者的 OS 与 CTX/ATRA 组无差异(P=0.20)。诊断时白细胞(WBC)计数较高(>10×10/l)与 CTX/ATRA 组 CIR 较高相关(P<0.001),而与 ATO/ATRA±CTX 组无关(P=0.48)。ATO 联合 ATRA 或 CTX/ATRA 对老年患者诱导缓解和巩固治疗是可行且有效的,特别是对诊断时 WBC 较高的患者。