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Incidence and non-genetic risk factors of irinotecan-induced severe neutropenia in Chinese adult inpatients

To analyze the incidence and nongenetic risk factors of irinotecan-induced severe neutropenia in the hospital, and provide additional reference and help for clinical treatment. A retrospective analysis of patients who received irinotecan based chemotherapy from May 2014 to May 2019 in Renmin Hospita...

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Autores principales: Zhang, Shuxiao, Yang, JingXiang, Zhan, Haiyan, Yang, Boning, Rong, PeiPei, Luo, Yi, Shi, Cai, Chen, Ying, Yang, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981354/
https://www.ncbi.nlm.nih.gov/pubmed/36862924
http://dx.doi.org/10.1097/MD.0000000000033005
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author Zhang, Shuxiao
Yang, JingXiang
Zhan, Haiyan
Yang, Boning
Rong, PeiPei
Luo, Yi
Shi, Cai
Chen, Ying
Yang, Jian
author_facet Zhang, Shuxiao
Yang, JingXiang
Zhan, Haiyan
Yang, Boning
Rong, PeiPei
Luo, Yi
Shi, Cai
Chen, Ying
Yang, Jian
author_sort Zhang, Shuxiao
collection PubMed
description To analyze the incidence and nongenetic risk factors of irinotecan-induced severe neutropenia in the hospital, and provide additional reference and help for clinical treatment. A retrospective analysis of patients who received irinotecan based chemotherapy from May 2014 to May 2019 in Renmin Hospital of Wuhan University was conducted. Univariate analysis and binary logistic regression analysis with the forward stepwise method were used to assess the risk factors associated with severe neutropenia induced by irinotecan. Of the 1312 patients treated with irinotecan-based regmines, only 612 patients met the inclusion criteria, and 32 patients developed irinotecan-induced severe neutropenia. In the univariate analysis, variables associated with severe neutropenia were tumor type, tumor stage, and therapeutic regimen. In the multivariate analysis, irinotecan plus lobaplatin, lung cancer or ovarian cancer, tumor stage T(2), T(3), and T(4), were identified as risk factors that contributed independently to irinotecan-induced severe neutropenia (P < .05), respectively. The results showed that the incidence of irinotecan–induced severe neutropenia was 5.23% in the hospital. The risk factors included tumor type (lung cancer or ovarian cancer), tumor stage (T(2), T(3), and T(4)) and therapeutic regimen (irinotecan plus lobaplatin). Therefore, for patients with these risk factors, it might be advisable to actively consider optimum management to reduce the occurrence of irinotecan–induced severe neutropenia.
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spelling pubmed-99813542023-03-04 Incidence and non-genetic risk factors of irinotecan-induced severe neutropenia in Chinese adult inpatients Zhang, Shuxiao Yang, JingXiang Zhan, Haiyan Yang, Boning Rong, PeiPei Luo, Yi Shi, Cai Chen, Ying Yang, Jian Medicine (Baltimore) 4200 To analyze the incidence and nongenetic risk factors of irinotecan-induced severe neutropenia in the hospital, and provide additional reference and help for clinical treatment. A retrospective analysis of patients who received irinotecan based chemotherapy from May 2014 to May 2019 in Renmin Hospital of Wuhan University was conducted. Univariate analysis and binary logistic regression analysis with the forward stepwise method were used to assess the risk factors associated with severe neutropenia induced by irinotecan. Of the 1312 patients treated with irinotecan-based regmines, only 612 patients met the inclusion criteria, and 32 patients developed irinotecan-induced severe neutropenia. In the univariate analysis, variables associated with severe neutropenia were tumor type, tumor stage, and therapeutic regimen. In the multivariate analysis, irinotecan plus lobaplatin, lung cancer or ovarian cancer, tumor stage T(2), T(3), and T(4), were identified as risk factors that contributed independently to irinotecan-induced severe neutropenia (P < .05), respectively. The results showed that the incidence of irinotecan–induced severe neutropenia was 5.23% in the hospital. The risk factors included tumor type (lung cancer or ovarian cancer), tumor stage (T(2), T(3), and T(4)) and therapeutic regimen (irinotecan plus lobaplatin). Therefore, for patients with these risk factors, it might be advisable to actively consider optimum management to reduce the occurrence of irinotecan–induced severe neutropenia. Lippincott Williams & Wilkins 2023-03-03 /pmc/articles/PMC9981354/ /pubmed/36862924 http://dx.doi.org/10.1097/MD.0000000000033005 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal.
spellingShingle 4200
Zhang, Shuxiao
Yang, JingXiang
Zhan, Haiyan
Yang, Boning
Rong, PeiPei
Luo, Yi
Shi, Cai
Chen, Ying
Yang, Jian
Incidence and non-genetic risk factors of irinotecan-induced severe neutropenia in Chinese adult inpatients
title Incidence and non-genetic risk factors of irinotecan-induced severe neutropenia in Chinese adult inpatients
title_full Incidence and non-genetic risk factors of irinotecan-induced severe neutropenia in Chinese adult inpatients
title_fullStr Incidence and non-genetic risk factors of irinotecan-induced severe neutropenia in Chinese adult inpatients
title_full_unstemmed Incidence and non-genetic risk factors of irinotecan-induced severe neutropenia in Chinese adult inpatients
title_short Incidence and non-genetic risk factors of irinotecan-induced severe neutropenia in Chinese adult inpatients
title_sort incidence and non-genetic risk factors of irinotecan-induced severe neutropenia in chinese adult inpatients
topic 4200
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981354/
https://www.ncbi.nlm.nih.gov/pubmed/36862924
http://dx.doi.org/10.1097/MD.0000000000033005
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