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
Hauptverfasser: Winzent‐Oonk, Shelby, Staley, Alyse, Alami, Vida, Bradley, Julie, Harvey, Susan, Pounds, Aneisia, Kuldanek, Susan, Pacenta, Holly, Winters, Amanda C., McKinney, Chris
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container_issue 1
container_start_page e31254
container_title Pediatric blood & cancer
container_volume 72
creator Winzent‐Oonk, Shelby
Staley, Alyse
Alami, Vida
Bradley, Julie
Harvey, Susan
Pounds, Aneisia
Kuldanek, Susan
Pacenta, Holly
Winters, Amanda C.
McKinney, Chris
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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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 &amp; 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 &amp; 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. 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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. 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source MEDLINE; Access via Wiley Online Library
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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