Jesamine Jany, Jan-Henrik Mikesch, Klaus Wethmar, David Baden, Irina Osiaevi, Georg Lenz, Christoph Schliemann, Alexander Pohlmann
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引用次数: 0
摘要
急性髓性白血病(AML)在诊断和治疗时与广泛变化的白细胞(WBC)计数相关。本研究检测了443例“7 + 3”强化治疗的AML患者白细胞动力学与预后的关系,并区分白细胞增多和非白细胞增多。通过对已知危险因素进行调整的回归分析,评估WBC最低点、曲线下面积(AUC)和负斜率等WBC动力学。白细胞增多与较差的总生存期相关(OS: HR 0.73;95% ci 0.569-0.938;p = 0.013),无事件生存期(EFS: HR 0.777;95% ci 0.625-0.966);p = 0.013)和早期死亡增加(ED: p = 0.017, AUC: HR 1.001;95% ci 1-1.003;p = 0.039)。相反,非白细胞增多患者的WBC最低点越低,生存期越短(HR 0.298;95% ci 0.118-0.751;p = 0.01),诱导时AUC下降(HR 0.981;95% ci 0.962-0.999;p = 0.041)。多变量分析在很大程度上证实了这些影响。
Prognostic impact of WBC kinetics after induction therapy in patients with acute myeloid leukemia (AML).
Acute myeloid leukemia (AML) is associated with broadly varying white blood cell (WBC) counts at the time of diagnosis and treatment. This study examined the association of WBC kinetics and outcome in 443 patients of '7 + 3' intensively treated AML patients, differentiating between leukocytosis and non-leukocytosis. WBC kinetics like WBC nadir, area under the curve (AUC) and negative slope were assessed by regression analyses adjusted for known risk factors. Leukocytosis was associated with inferior overall survival (OS: HR 0.73; 95% CI 0.569-0.938; p = 0.013), event-free survival (EFS: HR 0.777; 95% CI 0.625-0.966); p = 0.013) and increased early death (ED: p < 0.001) compared to the non-leukocytosis cohort. In patients with leukocytosis - regression analyses identified higher WBC nadir and higher AUC as predictors of worse outcome (WBC: HR 1.176; 95% CI 1.03-1.342; p = 0.017 and AUC: HR 1.001; 95% CI 1-1.003; p = 0.039). In contrary, non-leukocytosis patients presented an even shorter OS the lower their WBC nadir (HR 0.298; 95% CI 0.118-0.751; p = 0.01) and AUC dropped during induction (HR 0.981; 95% CI 0.962-0.999; p = 0.041). Multivariate analyses largely confirmed these effects.
期刊介绍:
Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor