Duggin Kelly, Tickle Kelly, Norman Gina, Yang Jie, Wang Chong, Cross Shane J, Gajjar Amar, Mandrell Belinda
St. Jude Children's Research Hospital, Memphis, TN, USA.
Stony Brook University, New York, NY, USA.
J Pediatr Oncol Nurs. 2014 Sep-Oct;31(5):277-83. doi: 10.1177/1043454214531090. Epub 2014 Jun 27.
Chemotherapy-induced nausea and vomiting are common and distressing side effects in patients with brain tumors and may be associated with radiation and the administration of highly emetogenic chemotherapy (HEC). Pediatric antiemetic guidelines recommend administration of a 5-hydroxytryptamine-3 (5HT3) receptor antagonists and the addition of aprepitant, a neurokinin 1 (NK1) antagonist with corticosteroids for the treatment of HEC. However, challenges persist in treating chemotherapy-induced nausea and vomiting in patients with brain tumors as corticosteroids are contraindicated due to potential impairment of the blood-brain barrier permeability. The objective was to determine whether a 5HT3 receptor antagonist and the addition of aprepitant, an NK1 antagonist without a corticosteroid, were effective in reducing HEC vomiting in pediatric brain tumor patients.
A retrospective review found that 18 patients with a history of high-grade vomiting during radiation were prescribed a 5HT3 receptor antagonist and aprepitant without a corticosteroid during their first course of HEC. To determine the efficacy of aprepitant without a corticosteroid, each recipient was matched with 2 controls who did not receiv aprepitant.
During HEC, controls without aprepitant were more likely to have Grade 2 or higher vomiting than the aprepitant recipients (P = .03; odds ratio = 4.15; 95% confidence interval = 1.59-10.82), after controlling for radiation-associated vomiting toxicity.
Significantly less vomiting was identified in children receiving HEC and prescribed a 5HT3 receptor antagonist and aprepitant. Findings suggest that the addition of an NK1 antagonist may be beneficial to emetic control in this highly vulnerable population.
化疗引起的恶心和呕吐是脑肿瘤患者常见且令人痛苦的副作用,可能与放疗及使用高度致吐性化疗药物(HEC)有关。儿科止吐指南建议使用5-羟色胺-3(5HT3)受体拮抗剂,并加用阿瑞匹坦(一种神经激肽1(NK1)拮抗剂)和皮质类固醇来治疗HEC。然而,由于皮质类固醇可能会损害血脑屏障通透性,因此在治疗脑肿瘤患者化疗引起的恶心和呕吐方面仍存在挑战。本研究的目的是确定5HT3受体拮抗剂加用阿瑞匹坦(一种不使用皮质类固醇的NK1拮抗剂)是否能有效减少小儿脑肿瘤患者的HEC呕吐。
一项回顾性研究发现,18例在放疗期间有高度呕吐史的患者在其首个HEC疗程中被开具了5HT3受体拮抗剂和不使用皮质类固醇的阿瑞匹坦。为了确定不使用皮质类固醇的阿瑞匹坦的疗效,将每位接受者与2名未接受阿瑞匹坦的对照者进行匹配。
在HEC期间,在控制了与放疗相关的呕吐毒性后,未使用阿瑞匹坦的对照者比使用阿瑞匹坦的接受者更有可能出现2级或更高程度的呕吐(P = 0.03;优势比 = 4.15;95%置信区间 = 1.59 - 10.82)。
在接受HEC并开具了5HT3受体拮抗剂和阿瑞匹坦的儿童中,呕吐明显较少。研究结果表明,加用NK1拮抗剂可能有助于控制这一高度脆弱人群的呕吐。