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本文引用的文献

1
Sunitinib-induced severe hypoglycemia in a diabetic patient.舒尼替尼致糖尿病患者严重低血糖症。
J Oncol Pharm Pract. 2014 Dec;20(6):469-72. doi: 10.1177/1078155213508441. Epub 2013 Oct 24.
2
Insulin requirements in patients with diabetes and declining kidney function: differences between insulin analogues and human insulin?糖尿病患者肾功能下降时的胰岛素需求:胰岛素类似物与人胰岛素有何不同?
Ther Adv Endocrinol Metab. 2013 Aug;4(4):113-21. doi: 10.1177/2042018813501188.
3
IGF-1 receptor is down-regulated by sunitinib induces MDM2-dependent ubiquitination.胰岛素样生长因子 1 受体受舒尼替尼下调诱导 MDM2 依赖性泛素化。
FEBS Open Bio. 2011 Dec 27;2:1-5. doi: 10.1016/j.fob.2011.12.001. Print 2012.
4
Effect of the tyrosine kinase inhibitors (sunitinib, sorafenib, dasatinib, and imatinib) on blood glucose levels in diabetic and nondiabetic patients in general clinical practice.酪氨酸激酶抑制剂(舒尼替尼、索拉非尼、达沙替尼和伊马替尼)对一般临床实践中糖尿病和非糖尿病患者血糖水平的影响。
J Oncol Pharm Pract. 2011 Sep;17(3):197-202. doi: 10.1177/1078155210378913. Epub 2010 Aug 4.
5
Blood glucose levels in patients with metastatic renal cell carcinoma treated with sunitinib.接受舒尼替尼治疗的转移性肾细胞癌患者的血糖水平
Br J Cancer. 2008 Nov 4;99(9):1380-2. doi: 10.1038/sj.bjc.6604709. Epub 2008 Oct 7.
6
Remission of diabetes while on sunitinib treatment for renal cell carcinoma.在接受舒尼替尼治疗肾细胞癌期间糖尿病缓解。
Ann Oncol. 2008 Apr;19(4):824-5. doi: 10.1093/annonc/mdn047. Epub 2008 Mar 6.
7
A quantitative analysis of kinase inhibitor selectivity.激酶抑制剂选择性的定量分析。
Nat Biotechnol. 2008 Jan;26(1):127-32. doi: 10.1038/nbt1358.
8
Toxicities associated with the administration of sorafenib, sunitinib, and temsirolimus and their management in patients with metastatic renal cell carcinoma.索拉非尼、舒尼替尼和替西罗莫司给药相关的毒性及其在转移性肾细胞癌患者中的管理。
Eur Urol. 2008 May;53(5):917-30. doi: 10.1016/j.eururo.2007.11.037. Epub 2007 Nov 26.
9
Current approaches for assessing insulin sensitivity and resistance in vivo: advantages, limitations, and appropriate usage.目前体内评估胰岛素敏感性和抵抗性的方法:优点、局限性及合理应用。
Am J Physiol Endocrinol Metab. 2008 Jan;294(1):E15-26. doi: 10.1152/ajpendo.00645.2007. Epub 2007 Oct 23.
10
Sunitinib versus interferon alfa in metastatic renal-cell carcinoma.舒尼替尼与干扰素α治疗转移性肾细胞癌的对比研究
N Engl J Med. 2007 Jan 11;356(2):115-24. doi: 10.1056/NEJMoa065044.

舒尼替尼对转移性肾细胞癌患者胰岛素清除率的早期影响。

The early effect of sunitinib on insulin clearance in patients with metastatic renal cell carcinoma.

作者信息

Thijs Anna Maria J, Tack Cees J, van der Graaf Winette T A, Rongen Gerard A, van Herpen Carla M L

机构信息

Department of Pharmacology-Toxicology, Radboudumc, Nijmegen.

Department of Medical Oncology, Radboudumc, Nijmegen.

出版信息

Br J Clin Pharmacol. 2016 Apr;81(4):768-72. doi: 10.1111/bcp.12797. Epub 2016 Jan 14.

DOI:10.1111/bcp.12797
PMID:26447463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4799938/
Abstract

AIMS

In patients with diabetes treated with sunitinib symptomatic hypoglycaemia has been reported. To explore the mechanism of this adverse effect we performed a prospective study to investigate the effect of sunitinib on insulin concentration, insulin clearance and insulin sensitivity.

METHODS

We studied the early effects of sunitinib on insulin sensitivity and insulin clearance with a hyperinsulinaemic euglycaemic clamp (insulin infusion rate 60 mU m−2 min−1; steady-state 90–120 min) in patients with renal cell carcinoma before and 1 week after the start of sunitinib 50 mg day−1. Insulin sensitivity index (SI) was defined as steady-state glucose disposal divided by the steady-state plasma insulin.

RESULTS

Ten patients (one with diabetes, treated with metformin) were included in the study protocol. Steady-state insulin concentrations during the clamp increased after 1 week of sunitinib (from 128.9 ± 9.0 mU l−1 to 170.8 ± 12.8 mU l−1, P < 0.05; 95% CI on difference − 64.3, −19.6). The calculated insulin sensitivity index decreased from 0.22 ± 0.04 before to 0.18 ± 0.02 μmol kg−1 min−1 per mU l−1 insulin (P < 0.05; 95% CI on difference 0.07, 0.08). As the insulin infusion rate was similar for both clamps, the increased steady-state insulin concentration indicates reduced insulin clearance.

CONCLUSION

Sunitinib affects insulin clearance which could possibly lead to overexposure to insulin in patients using insulin or insulin-secretion stimulating agents.

摘要

目的

有报道称,接受舒尼替尼治疗的糖尿病患者会出现症状性低血糖。为探究这种不良反应的机制,我们开展了一项前瞻性研究,以调查舒尼替尼对胰岛素浓度、胰岛素清除率和胰岛素敏感性的影响。

方法

我们采用高胰岛素正常血糖钳夹技术(胰岛素输注速率60 mU m−2 min−1;稳态90 - 120分钟),研究了50 mg/天舒尼替尼治疗开始前及开始后1周,舒尼替尼对肾细胞癌患者胰岛素敏感性和胰岛素清除率的早期影响。胰岛素敏感性指数(SI)定义为稳态葡萄糖处置量除以稳态血浆胰岛素水平。

结果

10例患者(1例糖尿病患者,正在接受二甲双胍治疗)纳入研究方案。舒尼替尼治疗1周后,钳夹期间的稳态胰岛素浓度升高(从128.9±9.0 mU l−1升至170.8±12.8 mU l−1,P<0.05;差值的95%置信区间为 - 64.3, - 19.6)。计算得出的胰岛素敏感性指数从之前的0.22±0.04降至0.18±0.02 μmol kg−1 min−1 per mU l−1胰岛素(P<0.05;差值的95%置信区间为0.07,0.08)。由于两次钳夹的胰岛素输注速率相似,稳态胰岛素浓度升高表明胰岛素清除率降低。

结论

舒尼替尼会影响胰岛素清除率,这可能导致使用胰岛素或胰岛素分泌刺激剂的患者胰岛素暴露过量。