纳武单抗在转移性肾细胞癌和终末期肾病透析患者中的疗效:病例报告和文献综述

Pub Date : 2018-06-13 eCollection Date: 2018-01-01 DOI:10.1155/2018/1623957
Jawaher Ansari, Muhammad Ali, Ashraf Farrag, Arwa M Ali, Abdulaziz Alhamad
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引用次数: 26

摘要

转移性肾细胞癌(mRCC)和终末期肾病(ESRD)患者的透析治疗带来了治疗挑战,特别是因为该患者组被排除在关键临床试验之外。此外,在药物剂量/药代动力学方面存在不确定性,缺乏安全性和有效性数据,并且当使用靶向治疗或免疫治疗来管理透析的mRCC患者时,可能会增加毒性。Nivolumab是一种抗程序性死亡-1免疫检查点抑制剂抗体,适用于既往接受过抗血管生成治疗的mRCC患者。鉴于上述不确定性,临床医生可能不愿意在这一患者群体中使用纳武单抗,从而可能导致延长生命的药物被拒绝。我们报告一位接受透析治疗的72岁mRCC和ESRD患者的病例,他接受了二线纳沃单抗治疗,并取得了良好的症状和放射学反应,并在22个多月的时间里保持无进展。此外,我们回顾了药代动力学数据,并发表了回顾性病例研究,以回顾mRCC和ESRD患者透析的管理选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Efficacy of Nivolumab in a Patient with Metastatic Renal Cell Carcinoma and End-Stage Renal Disease on Dialysis: Case Report and Literature Review.

Efficacy of Nivolumab in a Patient with Metastatic Renal Cell Carcinoma and End-Stage Renal Disease on Dialysis: Case Report and Literature Review.

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Efficacy of Nivolumab in a Patient with Metastatic Renal Cell Carcinoma and End-Stage Renal Disease on Dialysis: Case Report and Literature Review.

Treatment of patients with metastatic renal cell carcinoma (mRCC) and end-stage renal disease (ESRD) on dialysis poses a therapeutic challenge, particularly as this patient group was excluded from the pivotal clinical trials. In addition, there is uncertainty regarding drug dosing/pharmacokinetics, lack of safety and efficacy data, and potential for increased toxicity when using targeted therapy or immunotherapy for the management of patients with mRCC on dialysis. Nivolumab, an anti-programmed death-1 immune checkpoint inhibitor antibody, is indicated for the treatment of patients with mRCC who have received prior antiangiogenic therapy. Given the above-mentioned uncertainties, clinicians may be reluctant to use nivolumab for this patient population, leading to potential denial of life-prolonging medications. We report the case of a 72-year-old gentleman with mRCC and ESRD on dialysis who received second-line nivolumab therapy and achieved an excellent symptomatic and radiological response, remaining progression-free for over 22 months. In addition, we have reviewed the pharmacokinetic data and published retrospective case studies to review the management options for patients with mRCC and ESRD on dialysis.

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