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本文引用的文献

1
Lean thinking in health and nursing: an integrative literature review.健康与护理中的精益思维:一项综合文献综述。
Rev Lat Am Enfermagem. 2016 Aug 8;24:e2734. doi: 10.1590/1518-8345.0979.2734.
2
RandomizEd phase II trial of Sunitinib four weeks on and two weeks off versus Two weeks on and One week off in metastatic clear-cell type REnal cell carcinoma: RESTORE trial.舒尼替尼四周给药、两周停药与两周一疗程、一周停药治疗转移性透明细胞型肾细胞癌的随机 II 期临床试验:RESTORE 试验。
Ann Oncol. 2015 Nov;26(11):2300-5. doi: 10.1093/annonc/mdv357. Epub 2015 Sep 7.
3
Sunitinib dosing schedule 2/1 improves tolerability, efficacy, and health-related quality of life in Chinese patients with metastatic renal cell carcinoma.舒尼替尼2/1给药方案可提高中国转移性肾细胞癌患者的耐受性、疗效及健康相关生活质量。
Urol Oncol. 2015 Jun;33(6):268.e9-15. doi: 10.1016/j.urolonc.2015.03.008. Epub 2015 Apr 8.
4
Randomized, controlled, double-blind, cross-over trial assessing treatment preference for pazopanib versus sunitinib in patients with metastatic renal cell carcinoma: PISCES Study.随机、对照、双盲、交叉试验评估转移性肾细胞癌患者对帕唑帕尼与舒尼替尼的治疗偏好:PISCES 研究。
J Clin Oncol. 2014 May 10;32(14):1412-8. doi: 10.1200/JCO.2013.50.8267. Epub 2014 Mar 31.
5
Pazopanib versus sunitinib in metastatic renal-cell carcinoma.帕唑帕尼对比舒尼替尼用于转移性肾细胞癌。
N Engl J Med. 2013 Aug 22;369(8):722-31. doi: 10.1056/NEJMoa1303989.
6
Complete remission with tyrosine kinase inhibitors in renal cell carcinoma.肾细胞癌患者应用酪氨酸激酶抑制剂达到完全缓解。
J Clin Oncol. 2012 Feb 10;30(5):482-7. doi: 10.1200/JCO.2011.37.2516. Epub 2012 Jan 9.
7
What is value in health care?医疗保健中的价值是什么?
N Engl J Med. 2010 Dec 23;363(26):2477-81. doi: 10.1056/NEJMp1011024. Epub 2010 Dec 8.
8
Relationship between exposure to sunitinib and efficacy and tolerability endpoints in patients with cancer: results of a pharmacokinetic/pharmacodynamic meta-analysis.舒尼替尼暴露与癌症患者疗效和耐受性终点之间的关系:药代动力学/药效学的meta 分析结果。
Cancer Chemother Pharmacol. 2010 Jul;66(2):357-71. doi: 10.1007/s00280-009-1170-y. Epub 2009 Dec 5.
9
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.
10
Safety, pharmacokinetic, and antitumor activity of SU11248, a novel oral multitarget tyrosine kinase inhibitor, in patients with cancer.新型口服多靶点酪氨酸激酶抑制剂SU11248在癌症患者中的安全性、药代动力学及抗肿瘤活性
J Clin Oncol. 2006 Jan 1;24(1):25-35. doi: 10.1200/JCO.2005.02.2194. Epub 2005 Nov 28.

社区医疗实践中肾细胞癌的实用一线管理

Practical first-line management of renal cell carcinoma in a community practice.

作者信息

Conter Henry

机构信息

William Osler Health System, Brampton, ON, Canada.

出版信息

Can Urol Assoc J. 2016 Nov-Dec;10(11-12Suppl7):S239-S241. doi: 10.5489/cuaj.4295.

DOI:10.5489/cuaj.4295
PMID:28096935
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5215300/
Abstract

Sunitinib is an oral receptor tyrosine kinase inhibitor (TKI) that targets signalling by vascular endothelial growth factor receptors (VEGFRs). The standard sunitinib dosing schedule for metastatic renal cell carcinoma (mRCC) is 50 mg for four weeks (28 days) of treatment, followed by a two-week (14-day) break from treatment (four/two schedule). However, this schedule is associated with toxicities that can limit the patient's health-related quality of life (HRQOL) and impede treatment compliance. Given the generally incurable nature of mRCC and the toxicity associated with therapy, treatment strategies should focus on achieving long-term response, preserving HRQOL, and minimizing treatment-related toxicity. The William Osler Cancer Clinic in Brampton, ON, has instituted an alternative schedule of sunitinib treatment as our standard dosing strategy, involving two weeks of treatment, followed by a one-week break (two/one schedule), to minimize toxicity and improve HRQOL among their patients with mRCC.

摘要

舒尼替尼是一种口服受体酪氨酸激酶抑制剂(TKI),作用于血管内皮生长因子受体(VEGFRs)的信号传导。转移性肾细胞癌(mRCC)的舒尼替尼标准给药方案是50毫克,治疗四周(28天),然后停药两周(14天)(四/二方案)。然而,该方案会带来一些毒性反应,可能会限制患者的健康相关生活质量(HRQOL)并影响治疗依从性。鉴于mRCC通常无法治愈且治疗存在毒性,治疗策略应侧重于实现长期缓解、维持HRQOL并将治疗相关毒性降至最低。安大略省布兰普顿的威廉·奥斯勒癌症诊所已制定了舒尼替尼治疗的替代方案作为我们的标准给药策略,即治疗两周,然后停药一周(二/一方案),以尽量减少毒性并改善mRCC患者的HRQOL。