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培门冬酶联合化疗治疗急性淋巴细胞白血病与T细胞非霍奇金淋巴瘤的安全性分析

OBJECTIVE: To evaluate the safety of polyethylene glycol conjugated L-asparaginase (PEG-Asp) for patients with adult acute lymphoblastic leukemia (ALL) and T cell non-Hodgkin lymphoma (T-NHL). METHODS: A retrospective analysis was conducted on the clinical data of 101 young patients(≤40 years old) w...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342516/
https://www.ncbi.nlm.nih.gov/pubmed/25854457
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2015.03.001
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collection PubMed
description OBJECTIVE: To evaluate the safety of polyethylene glycol conjugated L-asparaginase (PEG-Asp) for patients with adult acute lymphoblastic leukemia (ALL) and T cell non-Hodgkin lymphoma (T-NHL). METHODS: A retrospective analysis was conducted on the clinical data of 101 young patients(≤40 years old) with ALL and T-NHL, diagnosed at Peking Union Medical College Hospital between January 2012 and June 2014. RESULTS: A total of 480 doses of PEG-Asp were administered in 44 cases with ALL and 57 patients with T-NHL. Only one patient (0.2%) experienced mild allergic reaction. Other grade 3 or 4 toxicities of non-hematologic effects included low level of fibrogen (6.4%), elevated ALT (4.4%), blood glucose (2.3%), and triglyceridemia (2.3%), decreased albumin (0.8%) and elevated amylase (0.2%). Furthermore, 5 cases (1.0%) developed venous thrombosis, 9 cases (1.9%) hemorrage, 1 patient (0.2%) non-necrosis pancretitis. CONCLUSION: The risk of allergic reaction incurred by PEG-Asp is very low. It can be used safely in ALL and T-NHL. Coagulation status should be monitored during the treatment.
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spelling pubmed-73425162020-07-16 培门冬酶联合化疗治疗急性淋巴细胞白血病与T细胞非霍奇金淋巴瘤的安全性分析 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To evaluate the safety of polyethylene glycol conjugated L-asparaginase (PEG-Asp) for patients with adult acute lymphoblastic leukemia (ALL) and T cell non-Hodgkin lymphoma (T-NHL). METHODS: A retrospective analysis was conducted on the clinical data of 101 young patients(≤40 years old) with ALL and T-NHL, diagnosed at Peking Union Medical College Hospital between January 2012 and June 2014. RESULTS: A total of 480 doses of PEG-Asp were administered in 44 cases with ALL and 57 patients with T-NHL. Only one patient (0.2%) experienced mild allergic reaction. Other grade 3 or 4 toxicities of non-hematologic effects included low level of fibrogen (6.4%), elevated ALT (4.4%), blood glucose (2.3%), and triglyceridemia (2.3%), decreased albumin (0.8%) and elevated amylase (0.2%). Furthermore, 5 cases (1.0%) developed venous thrombosis, 9 cases (1.9%) hemorrage, 1 patient (0.2%) non-necrosis pancretitis. CONCLUSION: The risk of allergic reaction incurred by PEG-Asp is very low. It can be used safely in ALL and T-NHL. Coagulation status should be monitored during the treatment. Editorial office of Chinese Journal of Hematology 2015-03 /pmc/articles/PMC7342516/ /pubmed/25854457 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2015.03.001 Text en 2015年版权归中华医学会所有 http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution 3.0 License (CC-BY-NC). The Copyright own by Publisher. Without authorization, shall not reprint, except this publication article, shall not use this publication format design. Unless otherwise stated, all articles published in this journal do not represent the views of the Chinese Medical Association or the editorial board of this journal.
spellingShingle 论著
培门冬酶联合化疗治疗急性淋巴细胞白血病与T细胞非霍奇金淋巴瘤的安全性分析
title 培门冬酶联合化疗治疗急性淋巴细胞白血病与T细胞非霍奇金淋巴瘤的安全性分析
title_full 培门冬酶联合化疗治疗急性淋巴细胞白血病与T细胞非霍奇金淋巴瘤的安全性分析
title_fullStr 培门冬酶联合化疗治疗急性淋巴细胞白血病与T细胞非霍奇金淋巴瘤的安全性分析
title_full_unstemmed 培门冬酶联合化疗治疗急性淋巴细胞白血病与T细胞非霍奇金淋巴瘤的安全性分析
title_short 培门冬酶联合化疗治疗急性淋巴细胞白血病与T细胞非霍奇金淋巴瘤的安全性分析
title_sort 培门冬酶联合化疗治疗急性淋巴细胞白血病与t细胞非霍奇金淋巴瘤的安全性分析
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342516/
https://www.ncbi.nlm.nih.gov/pubmed/25854457
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2015.03.001
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