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Prospective longitudinal evaluation of treatment-related toxicity and health-related quality of life during the first year of treatment for pediatric acute lymphoblastic leukemia
Background Pediatric acute lymphoblastic leukemia (ALL) therapy is accompanied by treatment-related toxicities (TRTs) and impaired quality of life. In Australia and New Zealand, children with ALL are treated with either Children's Oncology Group (COG) or international Berlin-Frankfurt-Munster (...
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Published in: | BMC cancer 2022-09, Vol.22 (1), p.1-985, Article 985 |
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description | Background Pediatric acute lymphoblastic leukemia (ALL) therapy is accompanied by treatment-related toxicities (TRTs) and impaired quality of life. In Australia and New Zealand, children with ALL are treated with either Children's Oncology Group (COG) or international Berlin-Frankfurt-Munster (iBFM) Study Group-based therapy. We conducted a prospective registry study to document symptomatic TRTs (venous thrombosis, neurotoxicity, pancreatitis and bone toxicity), compare TRT outcomes to retrospective TRT data, and measure the impact of TRTs on children's general and cancer-related health-related quality of life (HRQoL) and parents' emotional well-being. Methods Parents of children with newly diagnosed ALL were invited to participate in the ASSET (Acute Lymphoblastic Leukaemia Subtypes and Side Effects from Treatment) study and a prospective, longitudinal HRQoL study. TRTs were reported prospectively and families completed questionnaires for general (Healthy Utility Index Mark 3) and cancer specific (Pediatric Quality of Life Inventory (PedsQL)-Cancer Module) health related quality of life as well the Emotion Thermometer to assess emotional well-being. Results Beginning in 2016, 260 pediatric patients with ALL were enrolled on the TRT registry with a median age at diagnosis of 59 months (range 1-213 months), 144 males (55.4%), majority with Pre-B cell immunophenotype, n = 226 (86.9%), 173 patients (66.5%) treated according to COG platform with relatively equal distribution across risk classification sub-groups. From 2018, 79 families participated in the HRQoL study through the first year of treatment. There were 74 TRT recorded, reflecting a 28.5% risk of developing a TRT. Individual TRT incidence was consistent with previous studies, being 7.7% for symptomatic VTE, 11.9% neurotoxicity, 5.4% bone toxicity and 5.0% pancreatitis. Children's HRQoL was significantly lower than population norms throughout the first year of treatment. An improvement in general HRQoL, measured by the HUI3, contrasted with the lack of improvement in cancer-related HRQoL measured by the PedsQL Cancer Module over the first 12 months. There were no persisting differences in the HRQoL impact of COG compared to iBFM therapy. Conclusions It is feasible to prospectively monitor TRT incidence and longitudinal HRQoL impacts during ALL therapy. Early phases of ALL therapy, regardless of treatment platform, result in prolonged reductions in cancer-related HRQoL. Keywords: ALL, Health related q |
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In Australia and New Zealand, children with ALL are treated with either Children's Oncology Group (COG) or international Berlin-Frankfurt-Munster (iBFM) Study Group-based therapy. We conducted a prospective registry study to document symptomatic TRTs (venous thrombosis, neurotoxicity, pancreatitis and bone toxicity), compare TRT outcomes to retrospective TRT data, and measure the impact of TRTs on children's general and cancer-related health-related quality of life (HRQoL) and parents' emotional well-being. Methods Parents of children with newly diagnosed ALL were invited to participate in the ASSET (Acute Lymphoblastic Leukaemia Subtypes and Side Effects from Treatment) study and a prospective, longitudinal HRQoL study. TRTs were reported prospectively and families completed questionnaires for general (Healthy Utility Index Mark 3) and cancer specific (Pediatric Quality of Life Inventory (PedsQL)-Cancer Module) health related quality of life as well the Emotion Thermometer to assess emotional well-being. Results Beginning in 2016, 260 pediatric patients with ALL were enrolled on the TRT registry with a median age at diagnosis of 59 months (range 1-213 months), 144 males (55.4%), majority with Pre-B cell immunophenotype, n = 226 (86.9%), 173 patients (66.5%) treated according to COG platform with relatively equal distribution across risk classification sub-groups. From 2018, 79 families participated in the HRQoL study through the first year of treatment. There were 74 TRT recorded, reflecting a 28.5% risk of developing a TRT. Individual TRT incidence was consistent with previous studies, being 7.7% for symptomatic VTE, 11.9% neurotoxicity, 5.4% bone toxicity and 5.0% pancreatitis. Children's HRQoL was significantly lower than population norms throughout the first year of treatment. An improvement in general HRQoL, measured by the HUI3, contrasted with the lack of improvement in cancer-related HRQoL measured by the PedsQL Cancer Module over the first 12 months. There were no persisting differences in the HRQoL impact of COG compared to iBFM therapy. Conclusions It is feasible to prospectively monitor TRT incidence and longitudinal HRQoL impacts during ALL therapy. Early phases of ALL therapy, regardless of treatment platform, result in prolonged reductions in cancer-related HRQoL. Keywords: ALL, Health related quality of life, Treatment related toxicity, Quality of life, Psychosocial, Child, Registries</description><identifier>ISSN: 1471-2407</identifier><identifier>EISSN: 1471-2407</identifier><identifier>DOI: 10.1186/s12885-022-10072-x</identifier><identifier>PMID: 36109702</identifier><language>eng</language><publisher>London: BioMed Central Ltd</publisher><subject>Acute lymphoblastic leukemia ; Acute lymphocytic leukemia ; ALL ; Anxiety ; Beta cells ; Cancer ; Cancer therapies ; Care and treatment ; Child ; Children ; Children & youth ; Data collection ; Demographic aspects ; Emotions ; Evaluation ; Health aspects ; Health related quality of life ; Leukemia ; Methods ; Neurotoxicity ; Pancreatitis ; Parents & parenting ; Patients ; Pediatrics ; Psychosocial ; Quality of life ; Questionnaires ; Thromboembolism ; Thrombosis ; Treatment related toxicity ; Well being</subject><ispartof>BMC cancer, 2022-09, Vol.22 (1), p.1-985, Article 985</ispartof><rights>COPYRIGHT 2022 BioMed Central Ltd.</rights><rights>2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c605t-f8a5d42478f50f70ed6314599523dd1648d85802c8cd135aa894f1958e3825413</citedby><cites>FETCH-LOGICAL-c605t-f8a5d42478f50f70ed6314599523dd1648d85802c8cd135aa894f1958e3825413</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9479356/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2715495581?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids></links><search><creatorcontrib>Schilstra, Clarissa E</creatorcontrib><creatorcontrib>McCleary, Karen</creatorcontrib><creatorcontrib>Fardell, Joanna E</creatorcontrib><creatorcontrib>Donoghoe, Mark W</creatorcontrib><creatorcontrib>McCormack, Emma</creatorcontrib><creatorcontrib>Kotecha, Rishi S</creatorcontrib><creatorcontrib>Lourenco, Richard De Abreu</creatorcontrib><creatorcontrib>Ramachandran, Shanti</creatorcontrib><creatorcontrib>Cockcroft, Ruelleyn</creatorcontrib><creatorcontrib>Conyers, Rachel</creatorcontrib><creatorcontrib>Cross, Siobhan</creatorcontrib><creatorcontrib>Dalla-Pozza, Luciano</creatorcontrib><creatorcontrib>Downie, Peter</creatorcontrib><creatorcontrib>Revesz, Tamas</creatorcontrib><creatorcontrib>Osborn, Michael</creatorcontrib><creatorcontrib>Alvaro, Frank</creatorcontrib><creatorcontrib>Wakefield, Claire E</creatorcontrib><creatorcontrib>Marshall, Glenn M</creatorcontrib><creatorcontrib>Mateos, Marion K</creatorcontrib><creatorcontrib>Trahair, Toby N</creatorcontrib><title>Prospective longitudinal evaluation of treatment-related toxicity and health-related quality of life during the first year of treatment for pediatric acute lymphoblastic leukemia</title><title>BMC cancer</title><description>Background Pediatric acute lymphoblastic leukemia (ALL) therapy is accompanied by treatment-related toxicities (TRTs) and impaired quality of life. In Australia and New Zealand, children with ALL are treated with either Children's Oncology Group (COG) or international Berlin-Frankfurt-Munster (iBFM) Study Group-based therapy. We conducted a prospective registry study to document symptomatic TRTs (venous thrombosis, neurotoxicity, pancreatitis and bone toxicity), compare TRT outcomes to retrospective TRT data, and measure the impact of TRTs on children's general and cancer-related health-related quality of life (HRQoL) and parents' emotional well-being. Methods Parents of children with newly diagnosed ALL were invited to participate in the ASSET (Acute Lymphoblastic Leukaemia Subtypes and Side Effects from Treatment) study and a prospective, longitudinal HRQoL study. TRTs were reported prospectively and families completed questionnaires for general (Healthy Utility Index Mark 3) and cancer specific (Pediatric Quality of Life Inventory (PedsQL)-Cancer Module) health related quality of life as well the Emotion Thermometer to assess emotional well-being. Results Beginning in 2016, 260 pediatric patients with ALL were enrolled on the TRT registry with a median age at diagnosis of 59 months (range 1-213 months), 144 males (55.4%), majority with Pre-B cell immunophenotype, n = 226 (86.9%), 173 patients (66.5%) treated according to COG platform with relatively equal distribution across risk classification sub-groups. From 2018, 79 families participated in the HRQoL study through the first year of treatment. There were 74 TRT recorded, reflecting a 28.5% risk of developing a TRT. Individual TRT incidence was consistent with previous studies, being 7.7% for symptomatic VTE, 11.9% neurotoxicity, 5.4% bone toxicity and 5.0% pancreatitis. Children's HRQoL was significantly lower than population norms throughout the first year of treatment. An improvement in general HRQoL, measured by the HUI3, contrasted with the lack of improvement in cancer-related HRQoL measured by the PedsQL Cancer Module over the first 12 months. There were no persisting differences in the HRQoL impact of COG compared to iBFM therapy. Conclusions It is feasible to prospectively monitor TRT incidence and longitudinal HRQoL impacts during ALL therapy. Early phases of ALL therapy, regardless of treatment platform, result in prolonged reductions in cancer-related HRQoL. Keywords: ALL, Health related quality of life, Treatment related toxicity, Quality of life, Psychosocial, Child, Registries</description><subject>Acute lymphoblastic leukemia</subject><subject>Acute lymphocytic leukemia</subject><subject>ALL</subject><subject>Anxiety</subject><subject>Beta cells</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Care and treatment</subject><subject>Child</subject><subject>Children</subject><subject>Children & youth</subject><subject>Data collection</subject><subject>Demographic aspects</subject><subject>Emotions</subject><subject>Evaluation</subject><subject>Health aspects</subject><subject>Health related quality of life</subject><subject>Leukemia</subject><subject>Methods</subject><subject>Neurotoxicity</subject><subject>Pancreatitis</subject><subject>Parents & parenting</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Psychosocial</subject><subject>Quality of life</subject><subject>Questionnaires</subject><subject>Thromboembolism</subject><subject>Thrombosis</subject><subject>Treatment related toxicity</subject><subject>Well 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Lourenco, Richard De Abreu ; Ramachandran, Shanti ; Cockcroft, Ruelleyn ; Conyers, Rachel ; Cross, Siobhan ; Dalla-Pozza, Luciano ; Downie, Peter ; Revesz, Tamas ; Osborn, Michael ; Alvaro, Frank ; Wakefield, Claire E ; Marshall, Glenn M ; Mateos, Marion K ; Trahair, Toby N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c605t-f8a5d42478f50f70ed6314599523dd1648d85802c8cd135aa894f1958e3825413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Acute lymphoblastic leukemia</topic><topic>Acute lymphocytic leukemia</topic><topic>ALL</topic><topic>Anxiety</topic><topic>Beta cells</topic><topic>Cancer</topic><topic>Cancer therapies</topic><topic>Care and treatment</topic><topic>Child</topic><topic>Children</topic><topic>Children & youth</topic><topic>Data collection</topic><topic>Demographic aspects</topic><topic>Emotions</topic><topic>Evaluation</topic><topic>Health aspects</topic><topic>Health related quality of life</topic><topic>Leukemia</topic><topic>Methods</topic><topic>Neurotoxicity</topic><topic>Pancreatitis</topic><topic>Parents & parenting</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Psychosocial</topic><topic>Quality of life</topic><topic>Questionnaires</topic><topic>Thromboembolism</topic><topic>Thrombosis</topic><topic>Treatment related toxicity</topic><topic>Well being</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schilstra, Clarissa E</creatorcontrib><creatorcontrib>McCleary, Karen</creatorcontrib><creatorcontrib>Fardell, Joanna E</creatorcontrib><creatorcontrib>Donoghoe, Mark W</creatorcontrib><creatorcontrib>McCormack, Emma</creatorcontrib><creatorcontrib>Kotecha, Rishi S</creatorcontrib><creatorcontrib>Lourenco, Richard De Abreu</creatorcontrib><creatorcontrib>Ramachandran, Shanti</creatorcontrib><creatorcontrib>Cockcroft, Ruelleyn</creatorcontrib><creatorcontrib>Conyers, Rachel</creatorcontrib><creatorcontrib>Cross, Siobhan</creatorcontrib><creatorcontrib>Dalla-Pozza, Luciano</creatorcontrib><creatorcontrib>Downie, Peter</creatorcontrib><creatorcontrib>Revesz, Tamas</creatorcontrib><creatorcontrib>Osborn, Michael</creatorcontrib><creatorcontrib>Alvaro, Frank</creatorcontrib><creatorcontrib>Wakefield, Claire E</creatorcontrib><creatorcontrib>Marshall, Glenn M</creatorcontrib><creatorcontrib>Mateos, Marion K</creatorcontrib><creatorcontrib>Trahair, Toby N</creatorcontrib><collection>CrossRef</collection><collection>Science in Context</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital 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One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals(OpenAccess)</collection><jtitle>BMC cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schilstra, Clarissa E</au><au>McCleary, Karen</au><au>Fardell, Joanna E</au><au>Donoghoe, Mark W</au><au>McCormack, Emma</au><au>Kotecha, Rishi S</au><au>Lourenco, Richard De Abreu</au><au>Ramachandran, Shanti</au><au>Cockcroft, Ruelleyn</au><au>Conyers, Rachel</au><au>Cross, Siobhan</au><au>Dalla-Pozza, Luciano</au><au>Downie, Peter</au><au>Revesz, Tamas</au><au>Osborn, Michael</au><au>Alvaro, Frank</au><au>Wakefield, Claire E</au><au>Marshall, Glenn M</au><au>Mateos, Marion K</au><au>Trahair, Toby N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prospective longitudinal evaluation of treatment-related toxicity and health-related quality of life during the first year of treatment for pediatric acute lymphoblastic leukemia</atitle><jtitle>BMC cancer</jtitle><date>2022-09-15</date><risdate>2022</risdate><volume>22</volume><issue>1</issue><spage>1</spage><epage>985</epage><pages>1-985</pages><artnum>985</artnum><issn>1471-2407</issn><eissn>1471-2407</eissn><abstract>Background Pediatric acute lymphoblastic leukemia (ALL) therapy is accompanied by treatment-related toxicities (TRTs) and impaired quality of life. In Australia and New Zealand, children with ALL are treated with either Children's Oncology Group (COG) or international Berlin-Frankfurt-Munster (iBFM) Study Group-based therapy. We conducted a prospective registry study to document symptomatic TRTs (venous thrombosis, neurotoxicity, pancreatitis and bone toxicity), compare TRT outcomes to retrospective TRT data, and measure the impact of TRTs on children's general and cancer-related health-related quality of life (HRQoL) and parents' emotional well-being. Methods Parents of children with newly diagnosed ALL were invited to participate in the ASSET (Acute Lymphoblastic Leukaemia Subtypes and Side Effects from Treatment) study and a prospective, longitudinal HRQoL study. TRTs were reported prospectively and families completed questionnaires for general (Healthy Utility Index Mark 3) and cancer specific (Pediatric Quality of Life Inventory (PedsQL)-Cancer Module) health related quality of life as well the Emotion Thermometer to assess emotional well-being. Results Beginning in 2016, 260 pediatric patients with ALL were enrolled on the TRT registry with a median age at diagnosis of 59 months (range 1-213 months), 144 males (55.4%), majority with Pre-B cell immunophenotype, n = 226 (86.9%), 173 patients (66.5%) treated according to COG platform with relatively equal distribution across risk classification sub-groups. From 2018, 79 families participated in the HRQoL study through the first year of treatment. There were 74 TRT recorded, reflecting a 28.5% risk of developing a TRT. Individual TRT incidence was consistent with previous studies, being 7.7% for symptomatic VTE, 11.9% neurotoxicity, 5.4% bone toxicity and 5.0% pancreatitis. Children's HRQoL was significantly lower than population norms throughout the first year of treatment. An improvement in general HRQoL, measured by the HUI3, contrasted with the lack of improvement in cancer-related HRQoL measured by the PedsQL Cancer Module over the first 12 months. There were no persisting differences in the HRQoL impact of COG compared to iBFM therapy. Conclusions It is feasible to prospectively monitor TRT incidence and longitudinal HRQoL impacts during ALL therapy. Early phases of ALL therapy, regardless of treatment platform, result in prolonged reductions in cancer-related HRQoL. Keywords: ALL, Health related quality of life, Treatment related toxicity, Quality of life, Psychosocial, Child, Registries</abstract><cop>London</cop><pub>BioMed Central Ltd</pub><pmid>36109702</pmid><doi>10.1186/s12885-022-10072-x</doi><oa>free_for_read</oa></addata></record> |
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recordid | cdi_doaj_primary_oai_doaj_org_article_17592b5db9b04671b967107c72d358c2 |
source | Publicly Available Content Database (Proquest) (PQ_SDU_P3); PubMed Central(OpenAccess) |
subjects | Acute lymphoblastic leukemia Acute lymphocytic leukemia ALL Anxiety Beta cells Cancer Cancer therapies Care and treatment Child Children Children & youth Data collection Demographic aspects Emotions Evaluation Health aspects Health related quality of life Leukemia Methods Neurotoxicity Pancreatitis Parents & parenting Patients Pediatrics Psychosocial Quality of life Questionnaires Thromboembolism Thrombosis Treatment related toxicity Well being |
title | Prospective longitudinal evaluation of treatment-related toxicity and health-related quality of life during the first year of treatment for pediatric acute lymphoblastic leukemia |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T17%3A21%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Prospective%20longitudinal%20evaluation%20of%20treatment-related%20toxicity%20and%20health-related%20quality%20of%20life%20during%20the%20first%20year%20of%20treatment%20for%20pediatric%20acute%20lymphoblastic%20leukemia&rft.jtitle=BMC%20cancer&rft.au=Schilstra,%20Clarissa%20E&rft.date=2022-09-15&rft.volume=22&rft.issue=1&rft.spage=1&rft.epage=985&rft.pages=1-985&rft.artnum=985&rft.issn=1471-2407&rft.eissn=1471-2407&rft_id=info:doi/10.1186/s12885-022-10072-x&rft_dat=%3Cgale_doaj_%3EA717918412%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c605t-f8a5d42478f50f70ed6314599523dd1648d85802c8cd135aa894f1958e3825413%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2715495581&rft_id=info:pmid/36109702&rft_galeid=A717918412&rfr_iscdi=true |