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Predictors of Chemotherapy Induced Adverse Events in Pediatric Osteosarcoma Patients
OBJECTIVE: To investigate the prevalence of chemotherapy-induced adverse events and the associated risk factors in pediatric patients with osteosarcoma. METHODS: This retrospective cross-sectional study enrolled 90 pediatric osteosarcoma patients (with 1,017 chemotherapy cycles) treated at Srinagari...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
West Asia Organization for Cancer Prevention
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258668/ https://www.ncbi.nlm.nih.gov/pubmed/35092376 http://dx.doi.org/10.31557/APJCP.2022.23.1.93 |
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author | Sanguanboonyaphong, Phitjira Komvilaisak, Patcharee Suwannaying, Kunanya Yoodee, Jukapun Saeteaw, Manit Chanthawong, Suthan Subongkot, Suphat |
author_facet | Sanguanboonyaphong, Phitjira Komvilaisak, Patcharee Suwannaying, Kunanya Yoodee, Jukapun Saeteaw, Manit Chanthawong, Suthan Subongkot, Suphat |
author_sort | Sanguanboonyaphong, Phitjira |
collection | PubMed |
description | OBJECTIVE: To investigate the prevalence of chemotherapy-induced adverse events and the associated risk factors in pediatric patients with osteosarcoma. METHODS: This retrospective cross-sectional study enrolled 90 pediatric osteosarcoma patients (with 1,017 chemotherapy cycles) treated at Srinagarind Medical Center, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand, between January 1, 2008 and December 31, 2018. The prevalence of major adverse events and a correlation between baseline characteristics and adverse events were analyzed using a generalized estimating equation model. RESULT: The prevalence of adverse events in 90 pediatric osteosarcoma patients (with 1,017 chemotherapy cycles) was determined as chemotherapy-induced nausea and vomiting (29.2%; n=296), hepatotoxicity (21.2%; n=215), anemia (70.69%; n=719), neutropenia (26.65%; n=271), and thrombocytopenia (13.65%; n=139). Factors associated with chemotherapy-induced hepatotoxicity included methotrexate dose ≥ 12 g/m2 (odds ratio [OR] 1.30; 95% confidence interval [CI] 1.22–1.39; P<0.001), plasma concentration of methotrexate at 72 hours >0.1 μM (OR 1.22; 95% CI 1.19–1.25; P<0.001), and pre-hydration rate ≤ 125 mL/m(2)/h (OR 1.10; 95% CI 1.07–1.12; P<0.001). CONCLUSION: Major adverse events are becoming more common in pediatric osteosarcoma patients, and risk factors include larger chemotherapy doses, higher plasma methotrexate concentrations, and a slower pre-hydration rate. The outcomes of the study could aid in the better treatment of toxicity in children with osteosarcoma. |
format | Online Article Text |
id | pubmed-9258668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | West Asia Organization for Cancer Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-92586682022-07-06 Predictors of Chemotherapy Induced Adverse Events in Pediatric Osteosarcoma Patients Sanguanboonyaphong, Phitjira Komvilaisak, Patcharee Suwannaying, Kunanya Yoodee, Jukapun Saeteaw, Manit Chanthawong, Suthan Subongkot, Suphat Asian Pac J Cancer Prev Research Article OBJECTIVE: To investigate the prevalence of chemotherapy-induced adverse events and the associated risk factors in pediatric patients with osteosarcoma. METHODS: This retrospective cross-sectional study enrolled 90 pediatric osteosarcoma patients (with 1,017 chemotherapy cycles) treated at Srinagarind Medical Center, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand, between January 1, 2008 and December 31, 2018. The prevalence of major adverse events and a correlation between baseline characteristics and adverse events were analyzed using a generalized estimating equation model. RESULT: The prevalence of adverse events in 90 pediatric osteosarcoma patients (with 1,017 chemotherapy cycles) was determined as chemotherapy-induced nausea and vomiting (29.2%; n=296), hepatotoxicity (21.2%; n=215), anemia (70.69%; n=719), neutropenia (26.65%; n=271), and thrombocytopenia (13.65%; n=139). Factors associated with chemotherapy-induced hepatotoxicity included methotrexate dose ≥ 12 g/m2 (odds ratio [OR] 1.30; 95% confidence interval [CI] 1.22–1.39; P<0.001), plasma concentration of methotrexate at 72 hours >0.1 μM (OR 1.22; 95% CI 1.19–1.25; P<0.001), and pre-hydration rate ≤ 125 mL/m(2)/h (OR 1.10; 95% CI 1.07–1.12; P<0.001). CONCLUSION: Major adverse events are becoming more common in pediatric osteosarcoma patients, and risk factors include larger chemotherapy doses, higher plasma methotrexate concentrations, and a slower pre-hydration rate. The outcomes of the study could aid in the better treatment of toxicity in children with osteosarcoma. West Asia Organization for Cancer Prevention 2022-01 /pmc/articles/PMC9258668/ /pubmed/35092376 http://dx.doi.org/10.31557/APJCP.2022.23.1.93 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-Non Commercial 4.0 International License. https://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Research Article Sanguanboonyaphong, Phitjira Komvilaisak, Patcharee Suwannaying, Kunanya Yoodee, Jukapun Saeteaw, Manit Chanthawong, Suthan Subongkot, Suphat Predictors of Chemotherapy Induced Adverse Events in Pediatric Osteosarcoma Patients |
title | Predictors of Chemotherapy Induced Adverse Events in Pediatric Osteosarcoma Patients |
title_full | Predictors of Chemotherapy Induced Adverse Events in Pediatric Osteosarcoma Patients |
title_fullStr | Predictors of Chemotherapy Induced Adverse Events in Pediatric Osteosarcoma Patients |
title_full_unstemmed | Predictors of Chemotherapy Induced Adverse Events in Pediatric Osteosarcoma Patients |
title_short | Predictors of Chemotherapy Induced Adverse Events in Pediatric Osteosarcoma Patients |
title_sort | predictors of chemotherapy induced adverse events in pediatric osteosarcoma patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258668/ https://www.ncbi.nlm.nih.gov/pubmed/35092376 http://dx.doi.org/10.31557/APJCP.2022.23.1.93 |
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