The Tisch Cancer Institute, New York, NY, USA.
Institute for Translational Epidemiology and Department of Population Health Science and Policy, New York, NY, USA.
Carcinogenesis. 2019 Jul 4;40(5):651-660. doi: 10.1093/carcin/bgz014.
Acute promyelocytic leukemia (APL) is a particularly aggressive subtype of acute myeloid leukemia (AML), with high rates of early death. It is important to examine how epidemiological characteristics, clinical and treatment factors, cytogenetic and genetic data affect survival and differ between APL and non-APL AML patients. We analyzed population data from the New York State Cancer Registry to characterize AML including APL incidence rates by demographics. APL incidence rates were higher among Hispanics than non-Hispanics [incidence rate ratio = 1.22; 95% confidence interval (CI) = 1.02-1.43]; and among foreign-born than USA-born persons. APL incidence rates increased more rapidly through 1995-2014 than non-APL AML; and its frequency increased faster among foreign-born persons. In a hospital cohort of 390 AML patients, the risk of death was significantly higher among APL patients with FLT3-internal tandem duplications than those without [hazard ratio (HR) = 11.74; 95% CI = 1.03-134.5]; and among APL patients with secondary versus de novo disease (HR = 17.32; 95% CI = 1.56-192.1). Among non-APL AML patients, risk of death was significantly associated with prior chemotherapy with antitubulin agents after adjusting for age, gender and ethnicity (adjusted HR = 3.30; 95% CI = 1.49-7.32); and separately with older age, unfavorable cytogenetics and complex karyotype. This study highlights FLT3-internal tandem duplications as a prognostic factor in APL and proposes consideration of prior antitubulin therapy as a prognostic factor in non-APL AML.
急性早幼粒细胞白血病 (APL) 是一种特别具有侵袭性的急性髓系白血病 (AML) 亚型,早期死亡率较高。重要的是要研究流行病学特征、临床和治疗因素、细胞遗传学和遗传数据如何影响生存,并在 APL 和非 APL AML 患者之间存在差异。我们分析了纽约州癌症登记处的人群数据,以描述 AML 的发病率,包括按人口统计学特征划分的 APL 发病率。与非西班牙裔相比,西班牙裔的 APL 发病率更高[发病率比=1.22;95%置信区间 (CI)=1.02-1.43];与美国出生的人相比,出生在国外的人的 APL 发病率更高。1995 年至 2014 年期间,APL 的发病率增长速度快于非 APL AML;在国外出生的人中,其发病率增长速度更快。在一个包含 390 名 AML 患者的医院队列中,与无 FLT3 内部串联重复的 APL 患者相比,具有 FLT3 内部串联重复的 APL 患者的死亡风险显著更高[风险比 (HR)=11.74;95%CI=1.03-134.5];与继发疾病患者相比,具有原发性疾病的 APL 患者的死亡风险更高(HR=17.32;95%CI=1.56-192.1)。在非 APL AML 患者中,在调整年龄、性别和种族后,与蒽环类药物化疗后使用抗微管药物相关的死亡风险显著相关(调整后的 HR=3.30;95%CI=1.49-7.32);并分别与年龄较大、不良细胞遗传学和复杂核型相关。本研究强调了 FLT3 内部串联重复作为 APL 的预后因素,并提出将先前的抗微管治疗作为非 APL AML 的预后因素进行考虑。