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日本不良药物事件报告数据库中用于胃癌的抗癌药物相关急性肾损伤的评估。

Evaluation of Acute Kidney Injury Associated With Anticancer Drugs Used in Gastric Cancer in the Japanese Adverse Drug Event Report Database.

机构信息

Osaka University of Pharmaceutical Sciences, Takatsuki, Osaka, Japan.

Kumamoto University, Chuo-ku, Kumamoto, Japan.

出版信息

Ann Pharmacother. 2019 Dec;53(12):1200-1206. doi: 10.1177/1060028019865870. Epub 2019 Jul 26.

Abstract

Development of acute kidney injury (AKI) depends on the severity of renal dysfunction, clinical setting, comorbid factors, and geographical location. Gastric cancer is one of the deadliest malignancies worldwide, and its incidence is significantly high in Japan. We analyzed the rank-order of the association of anticancer agents for gastric cancer with AKI using a spontaneous reporting system database, the Japanese Adverse Drug Event Report database. We performed a retrospective pharmacovigilance disproportionality analysis using the adverse event reports submitted to the Pharmaceuticals and Medical Devices Agency between April 2004 and March 2017. Anticancer drug-related AKI was common in patients in their 60s and 70s (39.2% and 43.2%, respectively). AKI occurred most frequently within 1 month after anticancer drug administration. The signals of AKI were reported after treatment with S-1 (tegafur/gimeracil/oteracil), cisplatin (CDDP), and capecitabine, with significant adjusted reporting odds ratios (95% CI) of 1.50 (1.09-2.07), 3.43 (2.48-4.74), and 1.82 (1.15-2.90), respectively. CDDP-induced AKI was more likely to occur in patients who were male, hypertension, or diabetes mellitus. This study showed that most AKI cases were related to S-1 and/or CDDP adjuvant chemotherapy for gastric cancer treatment. The data also clarified that AKIs occurred within 1 month and that their clinical outcomes were more severe than previous reports of drug-induced AKI in general medicine. Our study provides useful information to minimize the risks of administration to patients at high risk for S-1 and/or CDDP containing chemotherapy-induced AKI.

摘要

急性肾损伤 (AKI) 的发生发展取决于肾功能不全的严重程度、临床环境、合并症因素和地理位置。胃癌是全球最致命的恶性肿瘤之一,在日本的发病率很高。我们使用自发报告系统数据库(日本药物不良反应报告数据库),分析了用于胃癌的抗癌药物与 AKI 之间关联的顺位。我们使用 2004 年 4 月至 2017 年 3 月向药品和医疗器械管理局提交的不良事件报告进行了回顾性药物警戒不比例性分析。抗癌药物相关 AKI 在 60 多岁和 70 多岁的患者中很常见(分别为 39.2%和 43.2%)。AKI 最常发生在抗癌药物给药后 1 个月内。在 S-1(替加氟/吉美嘧啶/奥替拉西)、顺铂(CDDP)和卡培他滨治疗后报告了 AKI 信号,经调整后的报告比值比(95%CI)分别为 1.50(1.09-2.07)、3.43(2.48-4.74)和 1.82(1.15-2.90)。CDDP 引起的 AKI 更可能发生在男性、高血压或糖尿病患者中。本研究表明,大多数 AKI 病例与 S-1 和/或 CDDP 辅助化疗治疗胃癌有关。这些数据还表明 AKI 发生在 1 个月内,其临床结局比一般医学中以前报告的药物引起的 AKI 更严重。我们的研究为最大限度地降低高危患者 S-1 和/或含 CDDP 的化疗引起 AKI 的风险提供了有用信息。

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