Incidence and survival for childhood cancer by endorsed non-stage prognostic indicators in Australia

被引:1
作者
Youlden, Danny R. [1 ,2 ,12 ]
Gupta, Sumit [3 ,4 ]
Frazier, A. Lindsay [5 ]
Moore, Andrew S. [6 ,7 ]
Gottardo, Nicholas G. [8 ,9 ]
Aitken, Joanne F. [1 ,10 ,11 ]
机构
[1] Canc Council Queensland, Viertel Canc Res Ctr, Brisbane, Qld, Australia
[2] Griffith Univ, Menzies Hlth Inst Queensland, Gold Coast, Qld, Australia
[3] Hosp Sick Children, Div Haematol Oncol, Toronto, ON, Canada
[4] Univ Toronto, Fac Med, Toronto, ON, Canada
[5] Dana Farber Boston Childrens Canc & Blood Disorder, Boston, MA USA
[6] Queensland Childrens Hosp, Oncol Serv, Brisbane, Qld, Australia
[7] Univ Queensland, Child Hlth Res Ctr, Brisbane, Qld, Australia
[8] Perth Childrens Hosp, Dept Paediat & Adolescent Oncol & Haematol, Perth, WA, Australia
[9] Univ Western Australia, Telethon Kids Canc Ctr, Telethon Kids Inst, Brain Tumor Res Program, Perth, WA, Australia
[10] Univ Queensland, Sch Publ Hlth, Brisbane, Qld, Australia
[11] Queensland Univ Technol, Sch Publ Hlth & Social Work, Brisbane, Qld, Australia
[12] Canc Council Queensland, POB 201, Brisbane, Qld 4001, Australia
关键词
Australia; childhood cancer; epidemiological studies; prognostic factors; survival analysis; CLASSIFICATION; DIAGNOSIS; CHILDREN;
D O I
10.1002/pbc.30889
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: An international expert panel recently recommended 15 'non-stage prognostic indicators' (NSPIs) across eight childhood cancers, classified as essential or additional, for collection in population-based cancer registries. We aimed to describe the incidence distribution and survival of each of these NSPIs.Procedures: Cases were extracted from the Australian Childhood Cancer Registry. The study cohort (n = 4187) comprised all children aged under 15 years diagnosed with an eligible cancer between 2010 and 2018, with follow-up until 31 December 2020. NSPI data were collected directly from each patient's medical records. Differences in 5-year relative survival were assessed using multivariable flexible parametric models, adjusted for sex and age group at diagnosis.Results: The availability of data varied, exceeding 85% for all essential NSPIs apart from histologic subtype for Wilms tumours (69%) and lineage for acute lymphoblastic leukaemia (78%). Information on additional NSPIs tended to be recorded less often, particularly cytogenetic subtype for non-alveolar rhabdomyosarcoma (28%) and astrocytoma (4%). Eight NSPIs exhibited a significant difference in survival, with the largest disparity occurring among children with astrocytoma according to tumour grade (5-year relative survival of 18% for grade IV disease compared with 99% for grade I disease; p < .001).Conclusions: Our findings demonstrate that most of the recommended NSPIs can be retrieved from medical records in Australia in recent years, allowing the capability of assessing survival within patient subgroups of clinical interest. Reporting of NSPI data has the capability to inform local and global understanding of population-level disparities in childhood cancer survival.
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页数:12
相关论文
共 19 条
[1]  
[Anonymous], 2011, Flexible Parametric Survival Analysis Using Stata: Beyond the Cox Model
[2]  
Brierley JD, 2017, TNM classification of malignant tumours
[3]  
Cancer Australia, 2008, A National Cancer Data Strategy for Australia
[4]   Global survival trends for brain tumors, by histology: Analysis of individual records for 67,776 children diagnosed in 61 countries during 2000-2014 (CONCORD-3) [J].
Girardi, Fabio ;
Di Carlo, Veronica ;
Stiller, Charles ;
Gatta, Gemma ;
Woods, Ryan R. ;
Visser, Otto ;
Lacour, Brigitte ;
Tucker, Thomas C. ;
Coleman, Michel P. ;
Allemani, Claudia .
NEURO-ONCOLOGY, 2023, 25 (03) :593-606
[5]  
Gupta S, 2020, LANCET ONCOL, V21, pE444, DOI 10.1016/S1470-2045(20)30320-X
[6]   Comparison of Apoptotic Inducing Effect of Zerumbone and Zerumbone-Loaded Nanostructured Lipid Carrier on Human Mammary Adenocarcinoma MDA-MB-231 Cell Line [J].
Hosseinpour, Mahnaz ;
Abdul, Ahmad Bustamam ;
Rahman, Heshu Sulaiman ;
Rasedee, Abdullah ;
Yeap, Swee Keong ;
Ahmadi, Negin ;
Othman, Hemn Hassan ;
Chartrand, Max Stanley .
JOURNAL OF NANOMATERIALS, 2014, 2014
[7]  
International Association of Cancer Registries, 2019, ICD O 32 2019
[8]   Striking Dichotomy in Outcome of MYCN-Amplified Neuroblastoma in the Contemporary Era [J].
Kushner, Brian H. ;
Modak, Shakeel ;
Kramer, Kim ;
LaQuaglia, Michael P. ;
Yataghene, Karima ;
Basu, Ellen M. ;
Roberts, Stephen S. ;
Cheung, Nai-Kong V. .
CANCER, 2014, 120 (13) :2050-2059
[9]   The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary [J].
Louis, David N. ;
Perry, Arie ;
Reifenberger, Guido ;
von Deimling, Andreas ;
Figarella-Branger, Dominique ;
Cavenee, Webster K. ;
Ohgaki, Hiroko ;
Wiestler, Otmar D. ;
Kleihues, Paul ;
Ellison, David W. .
ACTA NEUROPATHOLOGICA, 2016, 131 (06) :803-820
[10]   Outcome of Children with Standard-Risk T-Lineage Acute Lymphoblastic Leukemia-Comparison among Different Treatment Strategies [J].
Matloub, Yousif ;
Stork, Linda ;
Asselin, Barbara ;
Hunger, Stephen P. ;
Borowitz, Michael ;
Jones, Tamekia ;
Bostrom, Bruce ;
Gastier-Foster, Julie M. ;
Heerema, Nyla A. ;
Carroll, Andrew ;
Winick, Naomi ;
Carroll, William L. ;
Camitta, Bruce ;
Devidas, Meenakshi ;
Gaynon, Paul S. .
PEDIATRIC BLOOD & CANCER, 2016, 63 (02) :255-261