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肾功能损害对转移性结直肠癌患者接受三氟尿苷/替匹嘧啶治疗后严重中性粒细胞减少早期发展的影响。

Impact of renal impairment on early development of severe neutropenia with trifluridine/tipiracil treatment for metastatic colorectal cancer.

机构信息

Department of Clinical Pharmaceutics & Therapeutics, Faculty of Pharmaceutical Sciences, Hokkaido University of Science, 4-1, Maeda 7-jo 15-chome, Teine-ku, Sapporo, 006-8585, Japan.

Department of Pharmacy, Hokkaido University Hospital, Kita 14-jo, Nishi 5-chome, Kita-ku, Sapporo, 060-8648, Japan.

出版信息

Sci Rep. 2024 Nov 6;14(1):26990. doi: 10.1038/s41598-024-78741-4.

Abstract

Trifluridine/tipiracil (FTD/TPI) with or without bevacizumab is an effective treatment for metastatic colorectal cancer (mCRC). As this agent is mainly excreted via the kidney, we aimed to evaluate the impact of renal impairment (RI) on the early development of severe neutropenia, a dose-limiting toxicity and whose development reflects better treatment outcomes, in patients with mCRC treated with FTD/TPI. Patients with mCRC receiving FTD/TPI ± bevacizumab (n = 100) were divided into the RI group (creatinine clearance [CCr] < 90 mL/min) or control group (CCr ≥ 90 mL/min), and retrospectively evaluated. Severe neutropenia during the first two cycles occurred in 57.6% and 34.2% of patients in the RI and control groups, respectively, which was significantly different (P = 0.03) and met our primary endpoint. Furthermore, the incidence during the first cycle also differed significantly (52.5% in the RI group and 17.1% in the control group, P = 0.0004). Multivariate logistic regression analysis suggested that baseline RI and neutropenia were significant risk factors for early severe neutropenia (adjusted odds ratio and 95% confidence interval: 3.07, 1.24-7.59, P = 0.02 for RI, and 9.76, 1.08-88.11, P = 0.04 for neutropenia). In conclusion, our study suggested that patients with RI can exhibit early severe neutropenia during real-world FTD/TPI treatment for mCRC.

摘要

替氟尿苷/盐酸拓扑替康(FTD/TPI)联合或不联合贝伐珠单抗是转移性结直肠癌(mCRC)的有效治疗方法。由于该药物主要通过肾脏排泄,我们旨在评估肾功能不全(RI)对接受 FTD/TPI 治疗的 mCRC 患者严重中性粒细胞减少症(剂量限制毒性,其发展反映了更好的治疗效果)早期发展的影响。接受 FTD/TPI±贝伐珠单抗治疗的 mCRC 患者(n=100)分为 RI 组(肌酐清除率 [CCr]<90 mL/min)或对照组(CCr≥90 mL/min),并进行回顾性评估。RI 组和对照组患者在前两个周期中分别有 57.6%和 34.2%发生严重中性粒细胞减少症,差异具有统计学意义(P=0.03),达到了主要终点。此外,第一个周期的发生率也有显著差异(RI 组为 52.5%,对照组为 17.1%,P=0.0004)。多变量逻辑回归分析表明,基线 RI 和中性粒细胞减少症是早期严重中性粒细胞减少症的显著危险因素(调整后的优势比和 95%置信区间:RI 为 3.07,1.24-7.59,P=0.02;中性粒细胞减少症为 9.76,1.08-88.11,P=0.04)。总之,我们的研究表明,在接受 FTD/TPI 治疗 mCRC 的真实世界中,RI 患者可能会出现早期严重中性粒细胞减少症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1a1/11541766/34a9ea19ada5/41598_2024_78741_Fig1_HTML.jpg

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