{"title":"与 L-天冬酰胺酶治疗相关的儿童后可逆性脑病综合征:文献综述和六个病例报告。","authors":"María Margarita Tosta Pérez, Lisandra Herrera Belen, Adalberto Pessoa, Jorge Farías Avendaño","doi":"10.2174/0115748863290290240710161133","DOIUrl":null,"url":null,"abstract":"<p><p>L-asparaginase (L-ASNase) is an enzyme that shows targeted activity against Acute Lymphoblastic Leukemia (ALL) and similar lymphoid neoplasms by facilitating the breakdown of asparagine into L-aspartic acid, thereby reducing L-asparagine levels in leukemic cells. However, its therapeutic potential is hindered by its associated toxicity, leading to complications, such as thrombosis, hemorrhage, thrombocytopenia, fibrinolysis, hypersensitivity reactions, and the development of Posterior Reversible Encephalopathy Syndrome (PRES). This review compiles documented cases of PRES linked to treating B and T cell acute lymphoblastic leukemia in children using L-ASNase. Although this pathology is rare, understanding its management is crucial within ASNase-based chemotherapy protocols. As PRES lacks a specific treatment, focusing on symptomatic management becomes pivotal. Therefore, comprehending the underlying causes during L-ASNase treatment for acute lymphoblastic leukemia is essential. Understanding the etiology and clinical symptoms of this illness is critical for early diagnosis and treatment. The cases of PRES described in this review include instances in which this syndrome has appeared after the administration of L-ASNase in children. In some cases, PRES developed during induction therapy, while in others, it occurred during the reinduction phase. These cases resolved days after discontinuation of L-ASNase. 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引用次数: 0
摘要
L-天冬酰胺酶(L-ASNase)是一种对急性淋巴细胞白血病(ALL)和类似淋巴肿瘤具有靶向活性的酶,它能促进天冬酰胺分解成L-天冬氨酸,从而降低白血病细胞中的L-天冬酰胺水平。然而,天冬酰胺的治疗潜力因其相关毒性而受到阻碍,导致血栓形成、出血、血小板减少、纤维蛋白溶解、超敏反应和后可逆性脑病综合征(PRES)等并发症。本综述汇编了与使用 L-ASNase 治疗儿童 B 细胞和 T 细胞急性淋巴细胞白血病有关的 PRES 病例。虽然这种病理现象非常罕见,但了解其处理方法对于基于 ASNase 的化疗方案至关重要。由于 PRES 缺乏特异性治疗方法,对症治疗就变得至关重要。因此,在 L-ASNase 治疗急性淋巴细胞白血病的过程中,了解其根本原因至关重要。了解这种疾病的病因和临床症状对于早期诊断和治疗至关重要。本综述中描述的PRES病例包括在对儿童施用L-ASNase后出现这种综合征的病例。在一些病例中,PRES 是在诱导治疗期间出现的,而在另一些病例中,则是在再诱导阶段出现的。这些病例在停用 L-ASNase 几天后症状缓解。研究结果表明,用药与脑部病变的出现之间存在密切关系,当药物从血液中排出后,这些病变就会消失或减轻。
Posterior Reversible Encephalopathy Syndrome Associated with L-Asparaginase Treatment in Children: Literature Review and Six Case Reports.
L-asparaginase (L-ASNase) is an enzyme that shows targeted activity against Acute Lymphoblastic Leukemia (ALL) and similar lymphoid neoplasms by facilitating the breakdown of asparagine into L-aspartic acid, thereby reducing L-asparagine levels in leukemic cells. However, its therapeutic potential is hindered by its associated toxicity, leading to complications, such as thrombosis, hemorrhage, thrombocytopenia, fibrinolysis, hypersensitivity reactions, and the development of Posterior Reversible Encephalopathy Syndrome (PRES). This review compiles documented cases of PRES linked to treating B and T cell acute lymphoblastic leukemia in children using L-ASNase. Although this pathology is rare, understanding its management is crucial within ASNase-based chemotherapy protocols. As PRES lacks a specific treatment, focusing on symptomatic management becomes pivotal. Therefore, comprehending the underlying causes during L-ASNase treatment for acute lymphoblastic leukemia is essential. Understanding the etiology and clinical symptoms of this illness is critical for early diagnosis and treatment. The cases of PRES described in this review include instances in which this syndrome has appeared after the administration of L-ASNase in children. In some cases, PRES developed during induction therapy, while in others, it occurred during the reinduction phase. These cases resolved days after discontinuation of L-ASNase. The findings suggest a close relationship between drug administration and the appearance of brain lesions, as evidenced by the disappearance or decrease of these lesions when the drug was eliminated from the bloodstream.
期刊介绍:
Current Drug Safety publishes frontier articles on all the latest advances on drug safety. The journal aims to publish the highest quality research articles, reviews and case reports in the field. Topics covered include: adverse effects of individual drugs and drug classes, management of adverse effects, pharmacovigilance and pharmacoepidemiology of new and existing drugs, post-marketing surveillance. The journal is essential reading for all researchers and clinicians involved in drug safety.