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Cancer Diagn Progn. 2023 Jan 3;3(1):115-123. doi: 10.21873/cdp.10188. eCollection 2023 Jan-Feb.
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本文引用的文献

1
Microangiopathy associated with gemcitabine: a drug interaction with nab-paclitaxel? A case series and literature review.吉西他滨相关的微血管病变:与纳米白蛋白结合型紫杉醇存在药物相互作用?病例系列及文献综述
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2
[A case of thrombotic microangiopathy during chemotherapy with gemcitabine in a patient with pancreatic cancer].[一名胰腺癌患者在吉西他滨化疗期间发生血栓性微血管病的病例]
Nihon Shokakibyo Gakkai Zasshi. 2022;119(3):259-266. doi: 10.11405/nisshoshi.119.259.
3
Reversible renal-limited thrombotic microangiopathy due to gemcitabine-dexamethasone-cisplatin therapy: a case report.吉西他滨-地塞米松-顺铂治疗致可逆性肾性血栓性微血管病:病例报告。
BMC Nephrol. 2021 May 12;22(1):175. doi: 10.1186/s12882-021-02386-y.
4
Drug-induced thrombotic microangiopathy using the Japanese pharmacovigilance database.利用日本药物警戒数据库研究药物性血栓性微血管病
Int J Clin Pharmacol Ther. 2020 Oct;58(10):543-549. doi: 10.5414/CP203724.
5
A case of primary lung squamous cell carcinoma mimicking malignant mesothelioma producing granulocyte colony stimulating factor with chemotherapy (cisplatin and gemcitabine)-associated thrombotic thrombocytopenic purpura (TTP); An autopsy case report.一例原发性肺鳞癌模拟恶性间皮瘤产生粒细胞集落刺激因子伴化疗(顺铂和吉西他滨)相关血栓性血小板减少性紫癜(TTP);尸检病例报告。
Lung Cancer. 2019 Oct;136:105-108. doi: 10.1016/j.lungcan.2019.08.018. Epub 2019 Aug 20.
6
Thrombotic microangiopathy associated with gemcitabine use: Presentation and outcome in a national French retrospective cohort.与吉西他滨使用相关的血栓性微血管病:法国全国回顾性队列研究中的表现和结局。
Br J Clin Pharmacol. 2019 Feb;85(2):403-412. doi: 10.1111/bcp.13808. Epub 2018 Dec 18.
7
Gemcitabine-induced thrombotic microangiopathy with nephrotic syndrome.吉西他滨诱导的血栓性微血管病伴肾病综合征。
CEN Case Rep. 2018 Nov;7(2):217-220. doi: 10.1007/s13730-018-0332-3. Epub 2018 May 15.
8
Drug-induced thrombotic microangiopathy: a systematic review of published reports.药物诱导的血栓性微血管病:已发表报告的系统评价。
Blood. 2015 Jan 22;125(4):616-8. doi: 10.1182/blood-2014-11-611335. Epub 2014 Nov 20.
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Syndromes of thrombotic microangiopathy.血栓性微血管病的综合征。
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Gemcitabine-induced hemolytic uremic syndrome mimicking scleroderma renal crisis presenting with Raynaud's phenomenon, positive antinuclear antibodies and hypertensive emergency.吉西他滨诱导的溶血性尿毒症综合征,类似硬皮病肾危象,表现为雷诺现象、抗核抗体阳性及高血压急症。
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日本人群中吉西他滨诱导的血栓性微血管病的发病时间:病例系列和大规模药物警戒分析。

Time to Onset of Gemcitabine-induced Thrombotic Microangiopathy in a Japanese Population: A Case Series and Large-scale Pharmacovigilance Analysis.

作者信息

Takigawa Masaki, Tanaka Hiroyuki, Washiashi Hiromi, Onoda Toshihisa, Ishigami Akihito, Ishii Toshihiro

机构信息

Department of Pharmacy, Tokyo Metropolitan Geriatric Hospital, Tokyo, Japan.

Molecular Regulation of Aging, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan.

出版信息

Cancer Diagn Progn. 2023 Jan 3;3(1):115-123. doi: 10.21873/cdp.10188. eCollection 2023 Jan-Feb.

DOI:10.21873/cdp.10188
PMID:36632593
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9801453/
Abstract

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.

PATIENTS AND METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

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。

患者和方法

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。

结果

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。

结论

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。