Treatment and Survival in Acute Leukemia: A New South Wales Study Comparing Adolescents and Young Adults with Children and Adults

被引:0
|
作者
Li, Ming [1 ,2 ]
Anazodo, Antoinette [3 ,4 ,5 ,6 ]
Dalla-Pozza, Luciano [7 ]
Baeza, Paola Kabalan [8 ]
Roder, David [1 ,2 ]
Currow, David [9 ]
机构
[1] Canc Inst NSW, Sydney, NSW, Australia
[2] Univ South Australia, Adelaide, Australia
[3] Univ New South Wales, Sch Womens & Childrens Hlth, Randwick, Australia
[4] Kids Canc Ctr, Sydney, Australia
[5] Sydney Childrens Hosp, Randwick, Australia
[6] Westmead Hosp, Prince Wales Hosp Children, Nelune Comprehens Canc Ctr, Westmead, Australia
[7] Childrens Hosp Westmead, Canc Ctr Children, Westmead, Australia
[8] Hunter & Northern New South Wales Youth Canc Serv, Calvary Mater Newcastle, Australia
[9] Univ Wollongong, Fac Sci Med & Hlth, Wollongong, NSW, Australia
关键词
ACUTE LYMPHOBLASTIC-LEUKEMIA; CURE;
D O I
10.1155/2023/8600327
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. To investigate age differences in treatment and survival from acute lymphoblastic (ALL) and acute myeloid leukemia (AML). Methods. 1053 ALL/566 AML patients diagnosed in 2003-2015 on the New South Wales Cancer Registry were included. Treatment within 12 months from diagnosis was assessed using linked registry, hospital, and health-insurance data. Differences by age at diagnosis in treatment and survival were investigated using socio-demographically adjusted regression analyses, with adolescents and young adults (AYA, 15-24 years) as the reference category. Results. Children were less likely than AYA to start ALL treatment > 3 days from diagnosis (adjusted odds ratio (aOR 0.39, 95% CI 0.27-0.57)) and to have multiple treatment types (aOR 0.22, 95% CI 0.14-0.34). For AML, aOR of treatment start > 3 days was 0.16 (95% CI 0.09-0.29) for children compared with AYA, with no age differences in treatment types. Five-year disease-specific survival for ALL was 84%. Children were less likely than AYA to die from ALL (adjusted subhazard ratio (aSHR 0.32, 95% CI 0.22-0.50)). For AML, the corresponding survival was 73% without an age difference. Children having multiple treatment types for ALL had an increased risk of mortality at aSHR 2.67 (95% CI 1.53-4.67), but not adults at 1.26 (95% CI 0.67-2.47) (interaction p = 0.017). Time from diagnosis to initial treatment start and initial treatment type were not associated with mortality outcomes after adjusting for socio-demographic variables. Conclusion. Children with ALL had better survival. ALL Mortality were negatively associated with multiple treatment types.
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页数:12
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