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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 |
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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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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2087594404</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2087594404</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3538-61cc9bef32b2fd9b34200e950463dabef08856502f34b8a51ea78c67a9ffca853</originalsourceid><addsrcrecordid>eNp10bFO3TAUBmCrAhUKDH2ByhILHS44TpzYbJcrWiohtQPM0YlzQkwd-9Z2QGzduvYZ-yR1ucCA1MmWz6ffOvoJeV-w44IxfrLu9DFvuJJvyG4hKrEQrGi2Xu5M7ZB3Md5mWjMh35KdMr9Vistd8usMIlrjkOoRAuiEwcRkdKTgeurnpP2Ekfohz43tAzp6b9JINTiNgRpH04j03N1YE8c_P3_HNcJ3427oCoLpOgR3Spd0mm0yDpLxDiwNmILPUCdzl__1ow9pn2wPYCMePJ175PrT-dXqYnH59fOX1fJyoUtRykVdaK06HEre8aFXXVlxxlAJVtVlD3nApBS1YHwoq06CKBAaqesG1DBokKLcI0eb3HXwP2aMqZ1M1GgtOPRzbDmTjVBVxapMD1_RWz-HvEBWBWdNhkxl9XGjdN4pBhzadTAThIe2YO2_dtrcTvvYTrYfnhLnbsL-RT7XkcHJBtwbiw__T2q_na02kX8BfEWcBw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2120787509</pqid></control><display><type>article</type><title>Baseline characteristics and outcomes of children with cancer in the English‐speaking Caribbean: A multinational retrospective cohort</title><source>Wiley</source><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.</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 & 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 & 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. Continued data collection will allow evaluation of interventions and ensure maximal outcome improvements.</description><subject>Acute lymphoblastic leukemia</subject><subject>Acute myeloid leukemia</subject><subject>Brain tumors</subject><subject>Cancer</subject><subject>Caribbean</subject><subject>Cell lineage</subject><subject>child</subject><subject>Children</subject><subject>Complications</subject><subject>Data collection</subject><subject>Demographics</subject><subject>Demography</subject><subject>Hematology</subject><subject>Leukemia</subject><subject>low‐ and middle‐income countries</subject><subject>Lymphatic leukemia</subject><subject>Lymphocytes T</subject><subject>Lymphoma</subject><subject>Medical treatment</subject><subject>Medulloblastoma</subject><subject>Myeloid leukemia</subject><subject>Oncology</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Rhabdomyosarcoma</subject><subject>Solid tumors</subject><subject>survival outcomes</subject><subject>Tumors</subject><issn>1545-5009</issn><issn>1545-5017</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp10bFO3TAUBmCrAhUKDH2ByhILHS44TpzYbJcrWiohtQPM0YlzQkwd-9Z2QGzduvYZ-yR1ucCA1MmWz6ffOvoJeV-w44IxfrLu9DFvuJJvyG4hKrEQrGi2Xu5M7ZB3Md5mWjMh35KdMr9Vistd8usMIlrjkOoRAuiEwcRkdKTgeurnpP2Ekfohz43tAzp6b9JINTiNgRpH04j03N1YE8c_P3_HNcJ3427oCoLpOgR3Spd0mm0yDpLxDiwNmILPUCdzl__1ow9pn2wPYCMePJ175PrT-dXqYnH59fOX1fJyoUtRykVdaK06HEre8aFXXVlxxlAJVtVlD3nApBS1YHwoq06CKBAaqesG1DBokKLcI0eb3HXwP2aMqZ1M1GgtOPRzbDmTjVBVxapMD1_RWz-HvEBWBWdNhkxl9XGjdN4pBhzadTAThIe2YO2_dtrcTvvYTrYfnhLnbsL-RT7XkcHJBtwbiw__T2q_na02kX8BfEWcBw</recordid><startdate>201812</startdate><enddate>201812</enddate><creator>Gibson, T. N.</creator><creator>Beeput, S.</creator><creator>Gaspard, J.</creator><creator>George, C.</creator><creator>Gibson, D.</creator><creator>Jackson, N.</creator><creator>Leandre‐Broome, V.</creator><creator>Palmer‐Mitchell, N.</creator><creator>Alexis, C.</creator><creator>Bird‐Compton, J.</creator><creator>Bodkyn, C.</creator><creator>Boyle, R.</creator><creator>McLean‐Salmon, S.</creator><creator>Reece‐Mills, M.</creator><creator>Quee‐Brown, C. Sin</creator><creator>Allen, U.</creator><creator>Weitzman, S.</creator><creator>Blanchette, V.</creator><creator>Gupta, S.</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TK</scope><scope>7TO</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1334-3670</orcidid></search><sort><creationdate>201812</creationdate><title>Baseline characteristics and outcomes of children with cancer in the English‐speaking Caribbean: A multinational retrospective cohort</title><author>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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3538-61cc9bef32b2fd9b34200e950463dabef08856502f34b8a51ea78c67a9ffca853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Acute lymphoblastic leukemia</topic><topic>Acute myeloid leukemia</topic><topic>Brain tumors</topic><topic>Cancer</topic><topic>Caribbean</topic><topic>Cell lineage</topic><topic>child</topic><topic>Children</topic><topic>Complications</topic><topic>Data collection</topic><topic>Demographics</topic><topic>Demography</topic><topic>Hematology</topic><topic>Leukemia</topic><topic>low‐ and middle‐income countries</topic><topic>Lymphatic leukemia</topic><topic>Lymphocytes T</topic><topic>Lymphoma</topic><topic>Medical treatment</topic><topic>Medulloblastoma</topic><topic>Myeloid leukemia</topic><topic>Oncology</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Rhabdomyosarcoma</topic><topic>Solid tumors</topic><topic>survival outcomes</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric blood & cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gibson, T. 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 & 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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