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Fluoroquinolone prophylaxis does not increase risk of neuropathy in children with acute lymphoblastic leukemia

机译:氟代喹诺酮预防性不会增加急性淋巴细胞白血病儿童心肺病的风险

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Background Fluoroquinolone antibiotics are frequently utilized in pediatric oncology patients as prophylaxis or step‐down therapy following broad spectrum beta‐lactam therapy for febrile neutropenia. Concerns regarding neurotoxicity limit the use of these agents. No studies have evaluated the association between fluoroquinolone use and neurotoxicity in pediatric oncology patients receiving other neurotoxic agents such as vincristine. Methods An observational cohort study comprising patients aged 0‐18 at diagnosis enrolled on a prospective study for treatment of acute lymphoblastic leukemia (ALL) at a pediatric comprehensive cancer center between October 2007 and November 2018. Data for neuropathic pain and sensory or motor neuropathy were collected prospectively, and a Cox proportional hazards regression model was used to evaluate associations between administration of fluoroquinolone antibiotics during induction therapy and subsequent development of vincristine‐induced peripheral neurotoxicity (VIPN). Results A total of 598 participants were enrolled, including 338 (57%) who received fluoroquinolones during induction therapy; of these 470 (79%) were diagnosed with VIPN and 139 (23%) were diagnosed with high‐grade (Grade 3+) VIPN. On unadjusted analyses, and analyses adjusted for age and race, there was no evidence of an association between fluoroquinolone exposure and subsequent VIPN (hazard ratio [HR] 0.8, 95% CI 0.5‐1.04, P?=?.08) or high‐grade VIPN (HR 1.1, 95% CI 0.4‐2.2, P?=?.87). Conclusions The results of this observational study do not show an association between exposure to fluoroquinolone antibiotics during induction therapy for ALL and subsequent development of vincristine‐induced peripheral neuropathies, and suggest that a large increase in VIPN is unlikely.
机译:背景技术氟代喹啉酮抗生素经常用于儿科肿瘤患者作为预防性或降压疗法,这是发热中性蛋白的广谱β-内酰胺疗法。关于神经毒性的担忧限制了这些药剂的使用。没有研究在儿科肿瘤学患者接受其他神经毒性剂等的氟喹诺酮类使用和神经毒性之间的关联评估了含有其他神经毒性的。方法对诊断患者患者患者的观察队队列研究患者注册了2007年10月至2018年10月至11月在儿科综合癌症中心治疗急性淋巴细胞白血病(ALL)的前瞻性研究。神经病疼痛和感官或运动神经病变的数据预期收集的,并且Cox比例危害回归模型用于评估燃料喹啉酮抗生素在感应治疗期间的关联,随后的长春酮诱导的周围神经毒性(VIPN)。结果共有598名参与者,包括在感应治疗期间接受氟喹诺酮的338(57%);其中470(79%)被诊断为vipn,139(23%)被诊断为高级别(3次)vipn。在不调整的分析和年龄和种族的分析中,没有证据表明氟喹诺酮暴露和随后的vipn(危险比[hr] 0.8,95%ci 0.5-1.04,p?= 08)或高 - vipn等级(HR 1.1,95%CI 0.4-2.2,P?= 387)。结论该观察性研究的结果在感应治疗期间,在诱导的周围神经病的所有和随后发育的诱导治疗期间,在感应治疗期间没有显示出在氟代喹啉抗生素之间的关联,并表明VIPN的大量增加是不可能的。

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