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Baseline characteristics and outcomes of children with cancer in the English‐speaking Caribbean: A multinational retrospective cohort

Background English‐speaking Caribbean (ESC) childhood cancer outcomes are unknown. Procedure Through the SickKids‐Caribbean Initiative (SCI), we established a multicenter childhood cancer database across seven centers in six ESC countries. Data managers entered patient demographics, disease, treatme...

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Published in:Pediatric blood & cancer 2018-12, Vol.65 (12), p.e27298-n/a
Main Authors: Gibson, T. N., Beeput, S., Gaspard, J., George, C., Gibson, D., Jackson, N., Leandre‐Broome, V., Palmer‐Mitchell, N., Alexis, C., Bird‐Compton, J., Bodkyn, C., Boyle, R., McLean‐Salmon, S., Reece‐Mills, M., Quee‐Brown, C. Sin, Allen, U., Weitzman, S., Blanchette, V., Gupta, S.
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container_issue 12
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container_title Pediatric blood & cancer
container_volume 65
creator Gibson, T. N.
Beeput, S.
Gaspard, J.
George, C.
Gibson, D.
Jackson, N.
Leandre‐Broome, V.
Palmer‐Mitchell, N.
Alexis, C.
Bird‐Compton, J.
Bodkyn, C.
Boyle, R.
McLean‐Salmon, S.
Reece‐Mills, M.
Quee‐Brown, C. Sin
Allen, U.
Weitzman, S.
Blanchette, V.
Gupta, S.
description Background English‐speaking Caribbean (ESC) childhood cancer outcomes are unknown. Procedure Through the SickKids‐Caribbean Initiative (SCI), we established a multicenter childhood cancer database across seven centers in six ESC countries. Data managers entered patient demographics, disease, treatment, and outcome data. Data collection commenced in 2013, with retrospective collection to 2011 and subsequent prospective collection. Results A total of 367 children were diagnosed between 2011 and 2015 with a median age of 5.7 years (interquartile range 2.9–10.6 years). One hundred thirty (35.4%) patients were diagnosed with leukemia, 30 (8.2%) with lymphoma, and 149 (40.6%) with solid tumors. A relative paucity of children with brain tumors was seen (N = 58, 15.8%). Two‐year event‐free survival (EFS) for the cohort was 48.5% ± 3.2%; 2‐year overall survival (OS) was 55.1% ± 3.1%. Children with acute lymphoblastic leukemia (ALL) and Wilms tumor (WT) experienced better 2‐year EFS (62.1% ± 6.4% and 66.7% ± 10.1%), while dismal outcomes were seen in children with acute myeloid leukemia (AML; 22.7 ± 9.6%), rhabdomyosarcoma (21.0% ± 17.0%), and medulloblastoma (21.4% ± 17.8%). Of 108 deaths with known cause, 58 (53.7%) were attributed to disease and 50 (46.3%) to treatment complications. Death within 60 days of diagnosis was relatively common in acute leukemia [13/98 (13.3%) ALL, 8/26 (30.8%) AML]. Despite this, traditional prognosticators adversely impacted outcome in ALL, including higher age, higher white blood cell count, and T‐cell lineage. Conclusions ESC childhood cancer outcomes are significantly inferior to high‐income country outcomes. Based on these data, interventions for improving supportive care and modifying treatment protocols are under way. Continued data collection will allow evaluation of interventions and ensure maximal outcome improvements.
doi_str_mv 10.1002/pbc.27298
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N. ; Beeput, S. ; Gaspard, J. ; George, C. ; Gibson, D. ; Jackson, N. ; Leandre‐Broome, V. ; Palmer‐Mitchell, N. ; Alexis, C. ; Bird‐Compton, J. ; Bodkyn, C. ; Boyle, R. ; McLean‐Salmon, S. ; Reece‐Mills, M. ; Quee‐Brown, C. Sin ; Allen, U. ; Weitzman, S. ; Blanchette, V. ; Gupta, S.</creator><creatorcontrib>Gibson, T. N. ; Beeput, S. ; Gaspard, J. ; George, C. ; Gibson, D. ; Jackson, N. ; Leandre‐Broome, V. ; Palmer‐Mitchell, N. ; Alexis, C. ; Bird‐Compton, J. ; Bodkyn, C. ; Boyle, R. ; McLean‐Salmon, S. ; Reece‐Mills, M. ; Quee‐Brown, C. Sin ; Allen, U. ; Weitzman, S. ; Blanchette, V. ; Gupta, S.</creatorcontrib><description>Background English‐speaking Caribbean (ESC) childhood cancer outcomes are unknown. Procedure Through the SickKids‐Caribbean Initiative (SCI), we established a multicenter childhood cancer database across seven centers in six ESC countries. Data managers entered patient demographics, disease, treatment, and outcome data. Data collection commenced in 2013, with retrospective collection to 2011 and subsequent prospective collection. Results A total of 367 children were diagnosed between 2011 and 2015 with a median age of 5.7 years (interquartile range 2.9–10.6 years). One hundred thirty (35.4%) patients were diagnosed with leukemia, 30 (8.2%) with lymphoma, and 149 (40.6%) with solid tumors. A relative paucity of children with brain tumors was seen (N = 58, 15.8%). Two‐year event‐free survival (EFS) for the cohort was 48.5% ± 3.2%; 2‐year overall survival (OS) was 55.1% ± 3.1%. Children with acute lymphoblastic leukemia (ALL) and Wilms tumor (WT) experienced better 2‐year EFS (62.1% ± 6.4% and 66.7% ± 10.1%), while dismal outcomes were seen in children with acute myeloid leukemia (AML; 22.7 ± 9.6%), rhabdomyosarcoma (21.0% ± 17.0%), and medulloblastoma (21.4% ± 17.8%). Of 108 deaths with known cause, 58 (53.7%) were attributed to disease and 50 (46.3%) to treatment complications. Death within 60 days of diagnosis was relatively common in acute leukemia [13/98 (13.3%) ALL, 8/26 (30.8%) AML]. Despite this, traditional prognosticators adversely impacted outcome in ALL, including higher age, higher white blood cell count, and T‐cell lineage. Conclusions ESC childhood cancer outcomes are significantly inferior to high‐income country outcomes. Based on these data, interventions for improving supportive care and modifying treatment protocols are under way. Continued data collection will allow evaluation of interventions and ensure maximal outcome improvements.</description><identifier>ISSN: 1545-5009</identifier><identifier>EISSN: 1545-5017</identifier><identifier>DOI: 10.1002/pbc.27298</identifier><identifier>PMID: 30094928</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Acute lymphoblastic leukemia ; Acute myeloid leukemia ; Brain tumors ; Cancer ; Caribbean ; Cell lineage ; child ; Children ; Complications ; Data collection ; Demographics ; Demography ; Hematology ; Leukemia ; low‐ and middle‐income countries ; Lymphatic leukemia ; Lymphocytes T ; Lymphoma ; Medical treatment ; Medulloblastoma ; Myeloid leukemia ; Oncology ; Patients ; Pediatrics ; Rhabdomyosarcoma ; Solid tumors ; survival outcomes ; Tumors</subject><ispartof>Pediatric blood &amp; cancer, 2018-12, Vol.65 (12), p.e27298-n/a</ispartof><rights>2018 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3538-61cc9bef32b2fd9b34200e950463dabef08856502f34b8a51ea78c67a9ffca853</citedby><cites>FETCH-LOGICAL-c3538-61cc9bef32b2fd9b34200e950463dabef08856502f34b8a51ea78c67a9ffca853</cites><orcidid>0000-0003-1334-3670</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30094928$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gibson, T. N.</creatorcontrib><creatorcontrib>Beeput, S.</creatorcontrib><creatorcontrib>Gaspard, J.</creatorcontrib><creatorcontrib>George, C.</creatorcontrib><creatorcontrib>Gibson, D.</creatorcontrib><creatorcontrib>Jackson, N.</creatorcontrib><creatorcontrib>Leandre‐Broome, V.</creatorcontrib><creatorcontrib>Palmer‐Mitchell, N.</creatorcontrib><creatorcontrib>Alexis, C.</creatorcontrib><creatorcontrib>Bird‐Compton, J.</creatorcontrib><creatorcontrib>Bodkyn, C.</creatorcontrib><creatorcontrib>Boyle, R.</creatorcontrib><creatorcontrib>McLean‐Salmon, S.</creatorcontrib><creatorcontrib>Reece‐Mills, M.</creatorcontrib><creatorcontrib>Quee‐Brown, C. Sin</creatorcontrib><creatorcontrib>Allen, U.</creatorcontrib><creatorcontrib>Weitzman, S.</creatorcontrib><creatorcontrib>Blanchette, V.</creatorcontrib><creatorcontrib>Gupta, S.</creatorcontrib><title>Baseline characteristics and outcomes of children with cancer in the English‐speaking Caribbean: A multinational retrospective cohort</title><title>Pediatric blood &amp; cancer</title><addtitle>Pediatr Blood Cancer</addtitle><description>Background English‐speaking Caribbean (ESC) childhood cancer outcomes are unknown. Procedure Through the SickKids‐Caribbean Initiative (SCI), we established a multicenter childhood cancer database across seven centers in six ESC countries. Data managers entered patient demographics, disease, treatment, and outcome data. Data collection commenced in 2013, with retrospective collection to 2011 and subsequent prospective collection. Results A total of 367 children were diagnosed between 2011 and 2015 with a median age of 5.7 years (interquartile range 2.9–10.6 years). One hundred thirty (35.4%) patients were diagnosed with leukemia, 30 (8.2%) with lymphoma, and 149 (40.6%) with solid tumors. A relative paucity of children with brain tumors was seen (N = 58, 15.8%). Two‐year event‐free survival (EFS) for the cohort was 48.5% ± 3.2%; 2‐year overall survival (OS) was 55.1% ± 3.1%. Children with acute lymphoblastic leukemia (ALL) and Wilms tumor (WT) experienced better 2‐year EFS (62.1% ± 6.4% and 66.7% ± 10.1%), while dismal outcomes were seen in children with acute myeloid leukemia (AML; 22.7 ± 9.6%), rhabdomyosarcoma (21.0% ± 17.0%), and medulloblastoma (21.4% ± 17.8%). Of 108 deaths with known cause, 58 (53.7%) were attributed to disease and 50 (46.3%) to treatment complications. Death within 60 days of diagnosis was relatively common in acute leukemia [13/98 (13.3%) ALL, 8/26 (30.8%) AML]. Despite this, traditional prognosticators adversely impacted outcome in ALL, including higher age, higher white blood cell count, and T‐cell lineage. Conclusions ESC childhood cancer outcomes are significantly inferior to high‐income country outcomes. Based on these data, interventions for improving supportive care and modifying treatment protocols are under way. 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N.</au><au>Beeput, S.</au><au>Gaspard, J.</au><au>George, C.</au><au>Gibson, D.</au><au>Jackson, N.</au><au>Leandre‐Broome, V.</au><au>Palmer‐Mitchell, N.</au><au>Alexis, C.</au><au>Bird‐Compton, J.</au><au>Bodkyn, C.</au><au>Boyle, R.</au><au>McLean‐Salmon, S.</au><au>Reece‐Mills, M.</au><au>Quee‐Brown, C. Sin</au><au>Allen, U.</au><au>Weitzman, S.</au><au>Blanchette, V.</au><au>Gupta, S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Baseline characteristics and outcomes of children with cancer in the English‐speaking Caribbean: A multinational retrospective cohort</atitle><jtitle>Pediatric blood &amp; cancer</jtitle><addtitle>Pediatr Blood Cancer</addtitle><date>2018-12</date><risdate>2018</risdate><volume>65</volume><issue>12</issue><spage>e27298</spage><epage>n/a</epage><pages>e27298-n/a</pages><issn>1545-5009</issn><eissn>1545-5017</eissn><abstract>Background English‐speaking Caribbean (ESC) childhood cancer outcomes are unknown. Procedure Through the SickKids‐Caribbean Initiative (SCI), we established a multicenter childhood cancer database across seven centers in six ESC countries. Data managers entered patient demographics, disease, treatment, and outcome data. Data collection commenced in 2013, with retrospective collection to 2011 and subsequent prospective collection. Results A total of 367 children were diagnosed between 2011 and 2015 with a median age of 5.7 years (interquartile range 2.9–10.6 years). One hundred thirty (35.4%) patients were diagnosed with leukemia, 30 (8.2%) with lymphoma, and 149 (40.6%) with solid tumors. A relative paucity of children with brain tumors was seen (N = 58, 15.8%). Two‐year event‐free survival (EFS) for the cohort was 48.5% ± 3.2%; 2‐year overall survival (OS) was 55.1% ± 3.1%. Children with acute lymphoblastic leukemia (ALL) and Wilms tumor (WT) experienced better 2‐year EFS (62.1% ± 6.4% and 66.7% ± 10.1%), while dismal outcomes were seen in children with acute myeloid leukemia (AML; 22.7 ± 9.6%), rhabdomyosarcoma (21.0% ± 17.0%), and medulloblastoma (21.4% ± 17.8%). Of 108 deaths with known cause, 58 (53.7%) were attributed to disease and 50 (46.3%) to treatment complications. Death within 60 days of diagnosis was relatively common in acute leukemia [13/98 (13.3%) ALL, 8/26 (30.8%) AML]. Despite this, traditional prognosticators adversely impacted outcome in ALL, including higher age, higher white blood cell count, and T‐cell lineage. Conclusions ESC childhood cancer outcomes are significantly inferior to high‐income country outcomes. Based on these data, interventions for improving supportive care and modifying treatment protocols are under way. Continued data collection will allow evaluation of interventions and ensure maximal outcome improvements.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>30094928</pmid><doi>10.1002/pbc.27298</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-1334-3670</orcidid></addata></record>
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subjects Acute lymphoblastic leukemia
Acute myeloid leukemia
Brain tumors
Cancer
Caribbean
Cell lineage
child
Children
Complications
Data collection
Demographics
Demography
Hematology
Leukemia
low‐ and middle‐income countries
Lymphatic leukemia
Lymphocytes T
Lymphoma
Medical treatment
Medulloblastoma
Myeloid leukemia
Oncology
Patients
Pediatrics
Rhabdomyosarcoma
Solid tumors
survival outcomes
Tumors
title Baseline characteristics and outcomes of children with cancer in the English‐speaking Caribbean: A multinational retrospective cohort
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