Takigawa Masaki, Tanaka Hiroyuki, Washiashi Hiromi, Onoda Toshihisa, Ishigami Akihito, Ishii Toshihiro
Department of Pharmacy, Tokyo Metropolitan Geriatric Hospital, Tokyo, Japan.
Molecular Regulation of Aging, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan.
Cancer Diagn Progn. 2023 Jan 3;3(1):115-123. doi: 10.21873/cdp.10188. eCollection 2023 Jan-Feb.
BACKGROUND/AIM: Gemcitabine-induced thrombotic microangiopathy (G-TMA) is associated with a high mortality rate. However, owing to its low incidence, data on G-TMA remain limited. Therefore, a detailed review of G-TMA cases is critical to understand this adverse event. In addition, reviewing literature and pharmacovigilance analytics may be useful to characterise G-TMA. Here, time to onset of G-TMA was analysed based on available data.
We collected data for a case of TMA following gemcitabine administration at the Tokyo Metropolitan Geriatric Hospital. We also reviewed the literature on G-TMA cases in Japan from April 2000 to March 2022 to provide a case series. Moreover, we performed time-to-onset analysis of G-TMA using the data from the Japanese Adverse Drug Event Report (JADER) database.
Our case involved a patient with pancreatic cancer who developed thrombotic thrombocytopenic purpura 13 months after starting gemcitabine treatment. From the literature reviewed, in 14 out of 17 cases, G-TMA occurred 5-8 months after treatment initiation. The analysis of data from the JADER database showed that the median time to onset of G-TMA was 161 days. Weibull shape parameter analysis showed that the pattern of onset of G-TMA represented a random failure.
This study elucidated the time to onset of G-TMA in a Japanese population. Weibull shape parameter analysis showed that G-TMA may not necessarily develop in a dose-dependent manner. These results may be useful for monitoring G-TMA in the clinical setting.
背景/目的:吉西他滨诱导的血栓性微血管病(G-TMA)与高死亡率相关。然而,由于其发病率低,关于G-TMA的数据仍然有限。因此,对G-TMA病例进行详细回顾对于了解这一不良事件至关重要。此外,回顾文献和药物警戒分析可能有助于描述G-TMA的特征。在此,我们根据现有数据对G-TMA的发病时间进行了分析。
我们收集了东京都老人医院1例吉西他滨给药后发生血栓性微血管病的病例数据。我们还回顾了2000年4月至2022年3月期间日本G-TMA病例的文献,以提供一个病例系列。此外,我们使用日本药品不良反应报告(JADER)数据库的数据对G-TMA进行了发病时间分析。
我们的病例涉及一名胰腺癌患者,在开始吉西他滨治疗13个月后发生了血栓性血小板减少性紫癜。从回顾的文献来看,17例中有14例在治疗开始后5-8个月发生了G-TMA。对JADER数据库数据的分析表明,G-TMA的中位发病时间为161天。威布尔形状参数分析表明,G-TMA的发病模式代表随机失效。
本研究阐明了日本人群中G-TMA的发病时间。威布尔形状参数分析表明,G-TMA不一定以剂量依赖方式发生。这些结果可能有助于在临床环境中监测G-TMA。