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急性淋巴细胞白血病:基于监测、流行病学和最终结果(SEER)数据库的 1980-2017 年美国人群研究的结局。

Acute lymphoblastic leukemia: A population-based study of outcome in the United States based on the surveillance, epidemiology, and end results (SEER) database, 1980-2017.

机构信息

Department of Leukemia, U.T. M.D. Anderson Cancer Center, Houston, Texas.

Departments of Oncology and Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee.

出版信息

Am J Hematol. 2021 Jun 1;96(6):650-658. doi: 10.1002/ajh.26156. Epub 2021 Apr 1.

DOI:10.1002/ajh.26156
PMID:33709456
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9517941/
Abstract

The treatment in acute lymphoblastic Leukemia (ALL) has evolved and improved dramatically over the past four decades. We assessed the outcome of ALL overall, and the two major subsets of Philadelphia chromosome (Ph)-positive and Ph-negative ALL by age, time periods, ethnicity, median household income, and geographic county area. A total of 12 788 patients diagnosed with ALL from 1980 to 2017 were included. We performed an analysis to better evaluate the outcome evolution in ALL according to time period and patient's demographic factors. The overall 5-year survival rates have improved significantly over time, from 51% before 1990 to 72% since 2010. The survival rates for children (age 0 to 14 years) and adolescents (age 15 to 19 years) have improved from 73% and 55% before 1990 to 93% and 74% since 2010, respectively. Similarly, the rates had improved from 33% to 59% for adults 20 to 29 years old, 24% to 59% for 30 to 39 years old, and 14% to 43% for 40 to 59 years old between the two time periods. The rates remained under 30% in older patients (60+ years). Since 2010, patients with Ph-negative ALL had 5-year survival rate of 73% and those with Ph-positive ALL 50%. African Americans, Hispanic ethnicity, and lower household income were associated with inferior survival. The outcome of patients with ALL showed continued improvement across all age groups in the US. The recent introduction of targeted therapies, together with optimized supportive care, will continue to improve outcomes, particularly in older patients.

摘要

在过去的四十年中,急性淋巴细胞白血病(ALL)的治疗已经有了显著的发展和改善。我们根据年龄、时间段、种族、家庭收入中位数和地理县区域评估了 ALL 总体以及费城染色体(Ph)阳性和 Ph 阴性 ALL 的两个主要亚组的结果。共纳入了 1980 年至 2017 年期间诊断为 ALL 的 12788 例患者。我们进行了一项分析,以根据时间段和患者的人口统计学因素更好地评估 ALL 结果的演变。总体 5 年生存率随着时间的推移显著提高,从 1990 年前的 51%提高到 2010 年后的 72%。儿童(0 至 14 岁)和青少年(15 至 19 岁)的生存率从 1990 年前的 73%和 55%提高到 2010 年后的 93%和 74%。同样,20 至 29 岁的成年人、30 至 39 岁的成年人和 40 至 59 岁的成年人的生存率从两个时间段的 33%提高到 59%,24%提高到 59%,14%提高到 43%。年龄较大的患者(60 岁以上)的生存率仍低于 30%。自 2010 年以来,Ph 阴性 ALL 患者的 5 年生存率为 73%,Ph 阳性 ALL 患者为 50%。非裔美国人、西班牙裔和低收入家庭的收入与生存率较差相关。美国所有年龄段患者的 ALL 结果均持续改善。随着靶向治疗的引入以及优化的支持性护理,将继续改善结果,尤其是在老年患者中。

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