Acute leukemia incidence and patient survival among children and adults in the United States, 2001-2007

被引:471
作者
Dores, Graca M. [1 ,2 ]
Devesa, Susan S. [2 ]
Curtis, Rochelle E. [2 ]
Linet, Martha S. [2 ]
Morton, Lindsay M. [2 ]
机构
[1] Dept Vet Affairs Med Ctr, Oklahoma City, OK 73104 USA
[2] NCI, Div Canc Epidemiol & Genet, NIH, Dept Hlth & Human Serv, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
ACUTE PROMYELOCYTIC LEUKEMIA; ACUTE LYMPHOBLASTIC-LEUKEMIA; ACUTE MYELOID-LEUKEMIA; EARLY DEATH RATE; PROGNOSTIC-SIGNIFICANCE; INCIDENCE RATES; CHILDHOOD; SUBTYPE; HISPANICS; BLACKS;
D O I
10.1182/blood-2011-04-347872
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Since 2001, the World Health Organization classification for hematopoietic and lymphoid neoplasms has provided a framework for defining acute leukemia (AL) subtypes, although few population-based studies have assessed incidence patterns and patient survival accordingly. We assessed AL incidence rates (IRs), IR ratios (IRRs), and relative survival in the United States (2001-2007) in one of the first population-based, comprehensive assessments. Most subtypes of acute myeloid leukemia (AML) and acute lympho-blastic leukemia/lymphoma (ALL/L) predominated among males, from twice higher incidence of T-cell ALL/L among males than among females (IRR = 2.20) to nearly equal IRs of acute promyelocytic leukemia (APL; IRR = 1.08). Compared with non-Hispanic whites, Hispanics had significantly higher incidence of B-cell ALL/L (IRR = 1.64) and APL (IRR = 1.28); blacks had lower IRs of nearly all AL subtypes. All ALL/L but only some AML subtypes were associated with a bimodal age pattern. Among AML sub-types, survival was highest for APL and AML with inv(16). B-cell ALL/L had more favorable survival than T-cell ALL/L among the young; the converse occurred at older ages. Limitations of cancer registry data must be acknowledged, but the distinct AL incidence and survival patterns based on the World Health Organization classification support biologic diversity that should facilitate etiologic discovery, prognostication, and treatment advances. (Blood. 2012; 119(1): 34-43)
引用
收藏
页码:34 / 43
页数:10
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