Evaluating Asparaginase Toxicity in Hispanic Patients With Acute Lymphoblastic Leukemia in a Large Safety-Net Hospital.

IF 2.2 Q3 ONCOLOGY
World Journal of Oncology Pub Date : 2025-07-26 eCollection Date: 2025-08-01 DOI:10.14740/wjon2553
Dominick Zheng, Marcin Dragan, Jeffrey Jang, Sarah Tomassetti
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引用次数: 0

Abstract

Background: Acute lymphoblastic leukemia (ALL) is relatively rare in adults with poor rates of long-term remission. Chemotherapy protocols for adults have been adapted from pediatric protocols, including asparaginase. While asparaginase has shown significant efficacy in pediatric patients, its use in adults is limited due to hepatotoxicity, pancreatitis, and thrombosis. This study seeks to review the toxicity profile in Hispanic adults at a large safety-net hospital.

Methods: We performed a chart review of patients over the age of 18 with ALL treated with asparaginase. Data were collected between the years of 2015 and 2021 and included demographics, laboratory parameters on diagnosis, treatment details, and information on complications related to treatment.

Results: A total of 14 Hispanic patients diagnosed with ALL and treated with asparaginase from January 2016 to November 2021 were included in this study. Our patient population had an average body mass index (BMI) of 34 (standard deviation (SD) 8.7), with the majority (64%) classified as obese (BMI ≥ 30). Twelve patients (86%) were Philadelphia chromosome negative. The incidence of grade 3 to 4 hyperbilirubinemia (> 3 times the upper limit of normal (ULN) for serum bilirubin) was six out of 14 patients (43%). The incidence of grade 3 to 4 transaminitis (> 5 times the ULN for alanine aminotransferase (ALT) or aspartate aminotransferase (AST) levels) was 13 out of 14 patients (93%). Thrombosis occurred in six out of 14 patients (43%), with one patient experiencing disseminated intravascular coagulation (DIC).

Conclusions: Our cohort of Hispanic adults experienced transaminitis and hyperbilirubinemia at a high rate (93%). The higher incidence noted in our patients with class III obesity is in line with recent expert recommendations for dose reduction of asparaginase in patients with severe obesity. Our study suggests that our Hispanic population is at higher risk for developing hepatotoxicity after asparaginase use, though this could also be related to the high prevalence of obesity in our population. This is important for future care in selecting candidates for asparaginase therapy including those who may be at higher risk for adverse events.

在大型安全网医院评估西班牙裔急性淋巴细胞白血病患者的天冬酰胺酶毒性。
背景:急性淋巴细胞白血病(ALL)在成人中相对罕见,长期缓解率较差。成人化疗方案已改编自儿科方案,包括天冬酰胺酶。虽然天冬酰胺酶在儿科患者中显示出显著的疗效,但由于肝毒性、胰腺炎和血栓形成,其在成人中的应用受到限制。本研究旨在回顾在一家大型安全网医院的西班牙裔成年人的毒性概况。方法:我们对18岁以上接受天冬酰胺酶治疗的ALL患者进行了图表回顾。数据收集于2015年至2021年间,包括人口统计数据、诊断的实验室参数、治疗细节以及与治疗相关的并发症信息。结果:2016年1月至2021年11月,共有14名西班牙裔ALL患者接受了天冬酰胺酶治疗。我们的患者群体平均体重指数(BMI)为34(标准差(SD) 8.7),大多数(64%)被归类为肥胖(BMI≥30)。12例(86%)为费城染色体阴性。3 ~ 4级高胆红素血症(血胆红素正常值上限(ULN)的3倍)发生率为6 / 14(43%)。3 - 4级转氨酶的发生率为13 / 14(93%),是丙氨酸转氨酶(ALT)或天冬氨酸转氨酶(AST)水平的5倍。14例患者中有6例(43%)发生血栓形成,1例患者出现弥散性血管内凝血(DIC)。结论:我们的西班牙裔成人队列中出现转氨炎和高胆红素血症的比例很高(93%)。III级肥胖患者较高的发病率与最近专家建议的严重肥胖患者减少天冬酰胺酶剂量一致。我们的研究表明,西班牙裔人群在使用天冬酰胺酶后发生肝毒性的风险更高,尽管这也可能与我们人群中肥胖的高患病率有关。这对于未来选择天冬酰胺酶治疗的候选人,包括那些可能有较高不良事件风险的患者,是很重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.10
自引率
15.40%
发文量
37
期刊介绍: World Journal of Oncology, bimonthly, publishes original contributions describing basic research and clinical investigation of cancer, on the cellular, molecular, prevention, diagnosis, therapy and prognosis aspects. The submissions can be basic research or clinical investigation oriented. This journal welcomes those submissions focused on the clinical trials of new treatment modalities for cancer, and those submissions focused on molecular or cellular research of the oncology pathogenesis. Case reports submitted for consideration of publication should explore either a novel genomic event/description or a new safety signal from an oncolytic agent. The areas of interested manuscripts are these disciplines: tumor immunology and immunotherapy; cancer molecular pharmacology and chemotherapy; drug sensitivity and resistance; cancer epidemiology; clinical trials; cancer pathology; radiobiology and radiation oncology; solid tumor oncology; hematological malignancies; surgical oncology; pediatric oncology; molecular oncology and cancer genes; gene therapy; cancer endocrinology; cancer metastasis; prevention and diagnosis of cancer; other cancer related subjects. The types of manuscripts accepted are original article, review, editorial, short communication, case report, letter to the editor, book review.
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