Second primary acute lymphoblastic leukemia in adults: a SEER analysis of incidence and outcomes

被引:30
作者
Swaika, Abhisek [1 ,5 ]
Frank, Ryan D. [2 ]
Yang, Dongyun [3 ]
Finn, Laura E. [1 ]
Jiang, Liuyan [4 ]
Advani, Pooja [1 ]
Chanan-Khan, Asher A. [1 ,5 ]
Ailawadhi, Sikander [1 ,5 ]
Foran, James M. [1 ,5 ]
机构
[1] Mayo Clin, Div Hematol & Med Oncol, 4500 San Pablo Rd, Jacksonville, FL 32224 USA
[2] Mayo Clin, Div Biomed Stat & Informat, Rochester, MN USA
[3] Univ Southern Calif, Norris Comprehens Canc Ctr, Dept Prevent Med, Los Angeles, CA USA
[4] Mayo Clin, Dept Pathol & Lab Med, Div Hematopathol, Jacksonville, FL 32224 USA
[5] Mayo Clin, Ctr Canc, Jacksonville, FL 32224 USA
来源
CANCER MEDICINE | 2018年 / 7卷 / 02期
关键词
Second primary acute lymphoblastic leukemia; second primary ALL; SEER analysis; SIRs; standardized incidence ratios; POOR-PROGNOSIS; SECONDARY; THERAPY; CANCER; ABNORMALITIES; MALIGNANCIES; FEATURES;
D O I
10.1002/cam4.1266
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We conducted a surveillance epidemiology and end results (SEER)-based analysis to describe the incidence and characteristics of second primary acute lymphoblastic leukemia (sALL) among adults (>= 18 years) with a history of primary malignancies (1M). Standardized incidence ratios (SIRs) of sALL cases were calculated by site and 1M stage. We also evaluated the differences in 5-year sALL survival by age, site, and extent of 1M, latency of sALL after 1M, and evidence of underlying racial/ethnic disparity. We identified 10,956 patients with de-novo/primary acute lymphoblastic leukemia (1ALL) and 772 with sALL. Women (49.1% vs. 42.9%), white patients (72.0% vs. 59.5%), older patients (58.8% vs. 25.2%; age >= 65 years), and patients diagnosed between 2003 and 2012 (66.8% vs. 53.9%) had a higher proportion of sALL compared with 1ALL. There was a significantly inferior median 5-year survival for sALL patients compared to 1ALL (6 vs. 15 months; HR 1.20, 95% CI 1.10-1.31, P < 0.001). The median latency period was 60.0 months; the most common 1M among sALL patients were breast (17.9%) and prostate (17.4%). Patients with any 1M were at increased risk of developing sALL (SIR 1.76, 95% CI 1.58-1.95, P < 0.001). Hematological-1M sites had significantly higher SIRs (hematological-SIR 7.35; solid-SIR 1.33; P < 0.001). We observed a significant increase in sALL incidence after a 1M and a significantly worse 5-year survival with different demographic characteristics from 1ALL. There is a need to define appropriate screening methods for patients surviving their primary cancer.
引用
收藏
页码:499 / 507
页数:9
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