Clinical Pharmacy Department, Winchester District Memorial Hospital, Winchester, ON, Canada.
School of Pharmacy, University of Waterloo, Waterloo, ON, Canada.
Am J Case Rep. 2020 Jun 28;21:e924058. doi: 10.12659/AJCR.924058.
BACKGROUND Irinotecan, a topoisomerase I inhibitor, is a cytotoxic chemotherapeutic agent used to treat multiple malignancies, including those of colorectal, pancreatic, cervical, esophageal, gastric, and lung origin. Dysarthria, a state of difficult or unclear articulation of speech, has been reported as a rare side effect of irinotecan through multiple case reports and case series, but with limited published data aimed at understanding the underlying mechanism and effective management strategies. CASE REPORT We describe herein 3 cases of patients with pancreatic malignancy who experienced dysarthria while being treated with a chemotherapy regimen containing irinotecan at an ambulatory outpatient satellite chemotherapy site. All patients described received first-line FOLFIRINOX for pancreatic cancer and experienced dysarthria during their first infusion of irinotecan. In all cases, dysarthria was observed as a transient adverse drug reaction within the first 10 to 70 min of irinotecan infusion, which resolved rapidly upon pausing infusion without any long-term sequalae. All patients remained conscious and alert; physical and neurological examinations at dysarthria onset revealed no abnormalities. Some patients experienced distal extremity paresthesia, a known manifestation of oxaliplatin-induced acute neurotoxicity, and diaphoresis and nausea. Increased infusion time effectively prevented dysarthria during subsequent infusions. CONCLUSIONS Oncologists, pharmacists, nurses, and other care team members should be aware that irinotecan-associated dysarthria is a rare, mild, and self-limiting phenomenon to avoid inadvertently altering or withholding therapy. We suggest extending irinotecan infusion time, as opposed to dose reduction or treatment discontinuation, as a practical clinical management strategy for patients who develop recurrent dysarthria secondary to irinotecan infusion.
伊立替康是一种拓扑异构酶 I 抑制剂,属于细胞毒性化疗药物,用于治疗多种恶性肿瘤,包括结直肠癌、胰腺癌、宫颈癌、食管癌、胃癌和肺癌等。通过多项病例报告和病例系列研究报道,伊立替康的罕见副作用之一是构音障碍,即言语表达困难或不清晰,但目前针对其潜在机制和有效管理策略的研究数据有限。
本研究描述了在一家门诊卫星化疗点接受包含伊立替康的化疗方案治疗的 3 例胰腺癌患者出现构音障碍的情况。所有患者均接受 FOLFIRINOX 一线治疗胰腺癌,并在首次输注伊立替康时出现构音障碍。在所有情况下,构音障碍均表现为伊立替康输注后 10-70 分钟内的短暂药物不良反应,快速暂停输注后迅速缓解,无长期后遗症。所有患者均保持清醒和警觉;构音障碍发生时的体格检查和神经检查均未发现异常。一些患者出现了周围感觉异常,这是奥沙利铂引起的急性神经毒性的已知表现,同时还伴有出汗和恶心。增加输注时间可有效预防随后输注时出现构音障碍。
肿瘤学家、药剂师、护士和其他护理团队成员应认识到,伊立替康相关性构音障碍是一种罕见、轻微且自限性的现象,避免无意中改变或停止治疗。我们建议延长伊立替康输注时间,而不是减少剂量或停止治疗,作为因伊立替康输注而反复出现构音障碍的患者的一种实用临床管理策略。