Ifosfamide-Induced Neurotoxicity in Children with Solid Tumors: A Seven Year Retrospective Analysis of Incidence and Risk Factors.

IF 1 4区 医学 Q3 NURSING Journal of Pediatric Hematology-Oncology Nursing Pub Date : 2022-11-01 Epub Date: 2022-06-27 DOI:10.1177/27527530221090173
Kristen L Dalton
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引用次数: 1

Abstract

Background: Patients with cancer treated with the pro-drug ifosfamide may experience drug-induced neurotoxicity. Ifosfamide-induced neurotoxicity (IIN) is well described in the adult literature, but there is limited knowledge about this toxicity in pediatrics, especially in children with solid tumors. Methods: In this retrospective descriptive study, the author reviewed 7 years of clinical data regarding patients with solid tumors who received ifosfamide at a large, urban pediatric medical center. The author used descriptive statistics and logistic regression to describe the incidence of IIN and identify demographic and clinical factors most likely to be associated with the toxicity. Results: In a sample of 169 pediatric patients who received ifosfamide between 2011 and 2018, 13% developed symptoms of IIN. The author identified ifosfamide doses >2,000 mg/m2 to be a risk factor for IIN in the study sample (OR 17.82; 95 CI [2.17, 146.18]; p = .0073) and cited other variables as possible risk factors, though each could be linked to participants' ifosfamide exposure. Discussion: This study is the largest to describe IIN specifically in the pediatric solid tumor population. The study findings suggest the pattern of toxicity observed in adult patients should not be assumed in children. The author identified one risk factor that may predispose children to develop IIN and recommends further attention be paid to this toxicity in the pediatric population.

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异环磷酰胺诱导的儿童实体瘤神经毒性:7年发病率和危险因素回顾性分析
背景:用前药异环磷酰胺治疗的癌症患者可能会出现药物性神经毒性。异环磷酰胺引起的神经毒性(IIN)在成人文献中有很好的描述,但在儿科,特别是在患有实体瘤的儿童中,对这种毒性的了解有限。方法:在这项回顾性描述性研究中,作者回顾了在大型城市儿科医疗中心接受异环磷酰胺治疗的实体瘤患者7年的临床资料。作者使用描述性统计和逻辑回归来描述IIN的发生率,并确定最可能与毒性相关的人口统计学和临床因素。结果:在2011年至2018年期间接受异环磷酰胺治疗的169名儿科患者的样本中,13%出现了IIN症状。作者确定异环磷酰胺剂量>2,000 mg/m2是研究样本中IIN的危险因素(OR 17.82;95 ci [2.17, 146.18];P = 0.0073),并引用了其他变量作为可能的风险因素,尽管每个变量都可能与参与者的异环磷酰胺暴露有关。讨论:本研究是针对儿童实体肿瘤人群中IIN的最大研究。研究结果表明,在成人患者中观察到的毒性模式不应假设在儿童中。作者确定了一个可能使儿童易患IIN的风险因素,并建议进一步关注儿科人群中的这种毒性。
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