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黑人急性髓系白血病患者的生存状况较差,且遗传特征存在差异。

Poor Survival and Differential Impact of Genetic Features of Black Patients with Acute Myeloid Leukemia.

机构信息

The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.

The Ohio State University Comprehensive Cancer Center, Clara D. Bloomfield Center for Leukemia Outcomes Research, Columbus, Ohio.

出版信息

Cancer Discov. 2021 Mar;11(3):626-637. doi: 10.1158/2159-8290.CD-20-1579. Epub 2020 Dec 4.

Abstract

Clinical outcome of patients with acute myeloid leukemia (AML) is associated with cytogenetic and molecular factors and patient demographics (e.g., age and race). We compared survival of 25,523 non-Hispanic Black and White adults with AML using Surveillance Epidemiology and End Results (SEER) Program data and performed mutational profiling of 1,339 patients with AML treated on frontline Alliance for Clinical Trials in Oncology (Alliance) protocols. Black patients had shorter survival than White patients, both in SEER and in the setting of Alliance clinical trials. The disparity was especially pronounced in Black patients <60 years, after adjustment for socioeconomic (SEER) and molecular (Alliance) factors. Black race was an independent prognosticator of poor survival. Gene mutation profiles showed fewer and more mutations in younger Black patients. Overall survival of younger Black patients was adversely affected by mutations and -ITD, but, in contrast to White patients, was not improved by mutations. SIGNIFICANCE: We show that young Black patients have not benefited as much as White patients from recent progress in AML treatment in the United States. Our data suggest that both socioeconomic factors and differences in disease biology contribute to the survival disparity and need to be urgently addressed...

摘要

患者患有急性髓系白血病 (AML) 的临床结果与细胞遗传学和分子因素以及患者人口统计学特征(例如年龄和种族)有关。我们使用监测、流行病学和最终结果 (SEER) 计划的数据比较了 25523 名非西班牙裔黑人和白人成年 AML 患者的生存情况,并对接受一线肿瘤临床研究联盟 (Alliance) 方案治疗的 1339 名 AML 患者进行了突变分析。在 SEER 和 Alliance 临床试验中,黑种人患者的生存时间均短于白种人患者。在调整社会经济因素(SEER)和分子因素(Alliance)后,黑人患者的差异尤其明显。黑人种族是预后不良的独立预测因子。基因突变谱显示年轻黑人患者的突变较少,突变较多。年轻黑人患者的总生存时间受到突变和-ITD 的不利影响,但与白人患者不同,突变并未改善年轻黑人患者的生存时间。意义:我们表明,在美国,年轻的黑人患者并没有像白人患者那样从 AML 治疗的最新进展中获益。我们的数据表明,社会经济因素和疾病生物学的差异都导致了生存差异,需要紧急解决。

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