Risk of transfusion‐related iron overload varies based on oncologic diagnosis and associated treatment: Retrospective analysis from a single pediatric cancer center
Background Transfusion‐related iron overload (TRIO) is a widely acknowledged late effect of antineoplastic therapy in pediatric cancer survivors, but firm guidelines as to screening protocols or at‐risk populations are lacking in the literature. Procedure We performed retrospective analysis of all o...
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Veröffentlicht in: | Pediatric blood & cancer 2025-01, Vol.72 (1), p.e31254-n/a |
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description | Background
Transfusion‐related iron overload (TRIO) is a widely acknowledged late effect of antineoplastic therapy in pediatric cancer survivors, but firm guidelines as to screening protocols or at‐risk populations are lacking in the literature.
Procedure
We performed retrospective analysis of all oncology patients diagnosed at our center from 2014 to 2019, who underwent TRIO screening as part of an internal quality improvement project. Correlations of MRI‐confirmed TRIO with patient‐, disease‐, and treatment‐specific features were evaluated.
Results
We show that a tiered screening algorithm for TRIO, when followed as intended, led to the identification of the highest proportion of patients with TRIO. We confirm that cardiac TRIO is quite rare in the oncology patient population. However, accepted surrogate markers including red blood cell transfused volume and ferritin only modestly correlated with TRIO in our patient cohort. Instead, we found that older age, leukemia diagnosis, anthracycline exposure, and receipt of stem cell transplant were most strongly associated with risk for TRIO.
Conclusions
We describe associations between TRIO and patient, disease, and treatment characteristics in a multivariate risk model that could lead to an improved risk stratification of off‐therapy patients, and which should be validated in a prospective manner. |
doi_str_mv | 10.1002/pbc.31254 |
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Transfusion‐related iron overload (TRIO) is a widely acknowledged late effect of antineoplastic therapy in pediatric cancer survivors, but firm guidelines as to screening protocols or at‐risk populations are lacking in the literature.
Procedure
We performed retrospective analysis of all oncology patients diagnosed at our center from 2014 to 2019, who underwent TRIO screening as part of an internal quality improvement project. Correlations of MRI‐confirmed TRIO with patient‐, disease‐, and treatment‐specific features were evaluated.
Results
We show that a tiered screening algorithm for TRIO, when followed as intended, led to the identification of the highest proportion of patients with TRIO. We confirm that cardiac TRIO is quite rare in the oncology patient population. However, accepted surrogate markers including red blood cell transfused volume and ferritin only modestly correlated with TRIO in our patient cohort. Instead, we found that older age, leukemia diagnosis, anthracycline exposure, and receipt of stem cell transplant were most strongly associated with risk for TRIO.
Conclusions
We describe associations between TRIO and patient, disease, and treatment characteristics in a multivariate risk model that could lead to an improved risk stratification of off‐therapy patients, and which should be validated in a prospective manner.</description><identifier>ISSN: 1545-5009</identifier><identifier>ISSN: 1545-5017</identifier><identifier>EISSN: 1545-5017</identifier><identifier>DOI: 10.1002/pbc.31254</identifier><identifier>PMID: 39118250</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adolescent ; Anthracycline ; Cancer Survivors ; Child ; Child, Preschool ; Diagnosis ; Erythrocytes ; Female ; Ferritin ; Follow-Up Studies ; Humans ; Infant ; Iron overload ; Iron Overload - diagnosis ; Iron Overload - etiology ; Male ; Neoplasms - therapy ; Oncology ; Patients ; pediatric cancer survivorship ; Pediatrics ; Prognosis ; Quality control ; Retrospective Studies ; Risk Factors ; Stem cell transplantation ; transfusion ; Transfusion Reaction - blood</subject><ispartof>Pediatric blood & cancer, 2025-01, Vol.72 (1), p.e31254-n/a</ispartof><rights>2024 Wiley Periodicals LLC.</rights><rights>2025 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2434-c183d09878193400650bca1cffaa0258936fe04e2f5718e14c4cae10b574048b3</cites><orcidid>0000-0001-7916-7505</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpbc.31254$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpbc.31254$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39118250$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Winzent‐Oonk, Shelby</creatorcontrib><creatorcontrib>Staley, Alyse</creatorcontrib><creatorcontrib>Alami, Vida</creatorcontrib><creatorcontrib>Bradley, Julie</creatorcontrib><creatorcontrib>Harvey, Susan</creatorcontrib><creatorcontrib>Pounds, Aneisia</creatorcontrib><creatorcontrib>Kuldanek, Susan</creatorcontrib><creatorcontrib>Pacenta, Holly</creatorcontrib><creatorcontrib>Winters, Amanda C.</creatorcontrib><creatorcontrib>McKinney, Chris</creatorcontrib><title>Risk of transfusion‐related iron overload varies based on oncologic diagnosis and associated treatment: Retrospective analysis from a single pediatric cancer center</title><title>Pediatric blood & cancer</title><addtitle>Pediatr Blood Cancer</addtitle><description>Background
Transfusion‐related iron overload (TRIO) is a widely acknowledged late effect of antineoplastic therapy in pediatric cancer survivors, but firm guidelines as to screening protocols or at‐risk populations are lacking in the literature.
Procedure
We performed retrospective analysis of all oncology patients diagnosed at our center from 2014 to 2019, who underwent TRIO screening as part of an internal quality improvement project. Correlations of MRI‐confirmed TRIO with patient‐, disease‐, and treatment‐specific features were evaluated.
Results
We show that a tiered screening algorithm for TRIO, when followed as intended, led to the identification of the highest proportion of patients with TRIO. We confirm that cardiac TRIO is quite rare in the oncology patient population. However, accepted surrogate markers including red blood cell transfused volume and ferritin only modestly correlated with TRIO in our patient cohort. Instead, we found that older age, leukemia diagnosis, anthracycline exposure, and receipt of stem cell transplant were most strongly associated with risk for TRIO.
Conclusions
We describe associations between TRIO and patient, disease, and treatment characteristics in a multivariate risk model that could lead to an improved risk stratification of off‐therapy patients, and which should be validated in a prospective manner.</description><subject>Adolescent</subject><subject>Anthracycline</subject><subject>Cancer Survivors</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Diagnosis</subject><subject>Erythrocytes</subject><subject>Female</subject><subject>Ferritin</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Infant</subject><subject>Iron overload</subject><subject>Iron Overload - diagnosis</subject><subject>Iron Overload - etiology</subject><subject>Male</subject><subject>Neoplasms - therapy</subject><subject>Oncology</subject><subject>Patients</subject><subject>pediatric cancer survivorship</subject><subject>Pediatrics</subject><subject>Prognosis</subject><subject>Quality control</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Stem cell transplantation</subject><subject>transfusion</subject><subject>Transfusion Reaction - blood</subject><issn>1545-5009</issn><issn>1545-5017</issn><issn>1545-5017</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc9u1DAQhy1ERcvCgRdAlrjAYdtxbG8SbmXFn0qVQBWco4kzWbk4drCTrfbWR-ApeDCeBG-39IDEaUaab77R6MfYCwGnAqA4G1tzKkWh1SN2IrTSSw2ifPzQQ33MnqZ0ndEV6OoJO5a1EFWh4YT9urLpOw89nyL61M_JBv_79mckhxN13MbgedhSdAE7vsVoKfEWUx7tB94EFzbW8M7ixodkE0ffcUwpGHsnmCLhNJCf3vIrmmJII5nJbilz6Hb7hT6GgSNP1m8c8ZGyaopZadAbitzkXYrP2FGPLtHz-7pg3z68_7r-tLz8_PFifX65NIWSamlEJTuoq7IStVQAKw2tQWH6HhEKXdVy1RMoKnpdioqEMsogCWh1qUBVrVyw1wfvGMOPmdLUDDYZcg49hTk1EmqoVQn52oK9-ge9DnPMX2VKSFFqmQ9m6s2BMvn3FKlvxmgHjLtGQLMPr8nhNXfhZfblvXFuB-oeyL9pZeDsANxYR7v_m5ov79YH5R8iaqbY</recordid><startdate>202501</startdate><enddate>202501</enddate><creator>Winzent‐Oonk, Shelby</creator><creator>Staley, Alyse</creator><creator>Alami, Vida</creator><creator>Bradley, Julie</creator><creator>Harvey, Susan</creator><creator>Pounds, Aneisia</creator><creator>Kuldanek, Susan</creator><creator>Pacenta, Holly</creator><creator>Winters, Amanda C.</creator><creator>McKinney, Chris</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><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/0000-0001-7916-7505</orcidid></search><sort><creationdate>202501</creationdate><title>Risk of transfusion‐related iron overload varies based on oncologic diagnosis and associated treatment: Retrospective analysis from a single pediatric cancer center</title><author>Winzent‐Oonk, Shelby ; Staley, Alyse ; Alami, Vida ; Bradley, Julie ; Harvey, Susan ; Pounds, Aneisia ; Kuldanek, Susan ; Pacenta, Holly ; Winters, Amanda C. ; McKinney, Chris</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2434-c183d09878193400650bca1cffaa0258936fe04e2f5718e14c4cae10b574048b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><topic>Adolescent</topic><topic>Anthracycline</topic><topic>Cancer Survivors</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Diagnosis</topic><topic>Erythrocytes</topic><topic>Female</topic><topic>Ferritin</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Infant</topic><topic>Iron overload</topic><topic>Iron Overload - diagnosis</topic><topic>Iron Overload - etiology</topic><topic>Male</topic><topic>Neoplasms - therapy</topic><topic>Oncology</topic><topic>Patients</topic><topic>pediatric cancer survivorship</topic><topic>Pediatrics</topic><topic>Prognosis</topic><topic>Quality control</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Stem cell transplantation</topic><topic>transfusion</topic><topic>Transfusion Reaction - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Winzent‐Oonk, Shelby</creatorcontrib><creatorcontrib>Staley, Alyse</creatorcontrib><creatorcontrib>Alami, Vida</creatorcontrib><creatorcontrib>Bradley, Julie</creatorcontrib><creatorcontrib>Harvey, Susan</creatorcontrib><creatorcontrib>Pounds, Aneisia</creatorcontrib><creatorcontrib>Kuldanek, Susan</creatorcontrib><creatorcontrib>Pacenta, Holly</creatorcontrib><creatorcontrib>Winters, Amanda C.</creatorcontrib><creatorcontrib>McKinney, Chris</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><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>Winzent‐Oonk, Shelby</au><au>Staley, Alyse</au><au>Alami, Vida</au><au>Bradley, Julie</au><au>Harvey, Susan</au><au>Pounds, Aneisia</au><au>Kuldanek, Susan</au><au>Pacenta, Holly</au><au>Winters, Amanda C.</au><au>McKinney, Chris</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Risk of transfusion‐related iron overload varies based on oncologic diagnosis and associated treatment: Retrospective analysis from a single pediatric cancer center</atitle><jtitle>Pediatric blood & cancer</jtitle><addtitle>Pediatr Blood Cancer</addtitle><date>2025-01</date><risdate>2025</risdate><volume>72</volume><issue>1</issue><spage>e31254</spage><epage>n/a</epage><pages>e31254-n/a</pages><issn>1545-5009</issn><issn>1545-5017</issn><eissn>1545-5017</eissn><abstract>Background
Transfusion‐related iron overload (TRIO) is a widely acknowledged late effect of antineoplastic therapy in pediatric cancer survivors, but firm guidelines as to screening protocols or at‐risk populations are lacking in the literature.
Procedure
We performed retrospective analysis of all oncology patients diagnosed at our center from 2014 to 2019, who underwent TRIO screening as part of an internal quality improvement project. Correlations of MRI‐confirmed TRIO with patient‐, disease‐, and treatment‐specific features were evaluated.
Results
We show that a tiered screening algorithm for TRIO, when followed as intended, led to the identification of the highest proportion of patients with TRIO. We confirm that cardiac TRIO is quite rare in the oncology patient population. However, accepted surrogate markers including red blood cell transfused volume and ferritin only modestly correlated with TRIO in our patient cohort. Instead, we found that older age, leukemia diagnosis, anthracycline exposure, and receipt of stem cell transplant were most strongly associated with risk for TRIO.
Conclusions
We describe associations between TRIO and patient, disease, and treatment characteristics in a multivariate risk model that could lead to an improved risk stratification of off‐therapy patients, and which should be validated in a prospective manner.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>39118250</pmid><doi>10.1002/pbc.31254</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-7916-7505</orcidid></addata></record> |
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subjects | Adolescent Anthracycline Cancer Survivors Child Child, Preschool Diagnosis Erythrocytes Female Ferritin Follow-Up Studies Humans Infant Iron overload Iron Overload - diagnosis Iron Overload - etiology Male Neoplasms - therapy Oncology Patients pediatric cancer survivorship Pediatrics Prognosis Quality control Retrospective Studies Risk Factors Stem cell transplantation transfusion Transfusion Reaction - blood |
title | Risk of transfusion‐related iron overload varies based on oncologic diagnosis and associated treatment: Retrospective analysis from a single pediatric cancer center |
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