• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

舒尼替尼治疗转移性肾细胞癌(mRCC)患者的经验:来自西班牙 3 项观察性前瞻性研究的汇总分析。

Experience with Sunitinib in metastatic renal cell carcinoma (mRCC) patients: pooled analysis from 3 Spanish observational prospective studies.

机构信息

a Hospital Universitario 12 de Octubre , Madrid , Spain.

b Medical Oncology , Hospital de la Santa Creu i Sant Pau , Barcelona , Spain.

出版信息

Expert Opin Drug Saf. 2018 Jun;17(6):573-579. doi: 10.1080/14740338.2017.1330410. Epub 2017 Aug 28.

DOI:10.1080/14740338.2017.1330410
PMID:28535693
Abstract

BACKGROUND

A pivotal, randomized, phase III trial demonstrated a statistically significant superiority of sunitinib over interferon-α in metastatic renal cell carcinoma (mRCC) patients.

OBJECTIVE

To evaluate the effectiveness and safety of sunitinib in patients with advanced or mRCC in routine clinical practice.

METHODS

Retrospective pooled analysis of clinical data from three observational and prospective studies carried out between 2007 and 2011 in 33 Spanish hospitals. Tumor response, Progression-free survival (PFS) and overall survival (OS), and main sunitinib-related toxicities were registered.

RESULTS

224 patients were analyzed. Median PFS 10.6 months (95% CI: 9.02-12.25), median OS 21.9 months (95% CI: 17.2-26.6). Objective response rate (ORR) 43.8% (95% CI: 36.8-50.7). Median time to PR was 3.8 months (95% CI: 3.86-5.99) and to CR 8.2 months (95% CI: 4.75-9.77). The most common ≥ grade-3 AEs were asthenia/fatigue (18.7%), hand-foot syndrome (6.2%), hypertension (5.8%) and neutropenia (4.8%). Hand-foot syndrome, diarrhea and mucositis were confirmed as independent predictors for PFS and/or OS in a multivariate analysis (p < 0.05) Conclusions: Outcomes with sunitinib in daily clinical practice resemble those obtained in clinical trials. Long-term benefit with sunitinib is possible in advanced RCC patients but the appropriate management of toxicities is mandatory to enable patients to remain on treatment.

摘要

背景

一项关键性、随机、III 期试验表明舒尼替尼在转移性肾细胞癌(mRCC)患者中的疗效明显优于干扰素-α。

目的

评估舒尼替尼在常规临床实践中治疗晚期或 mRCC 患者的疗效和安全性。

方法

回顾性分析了 2007 年至 2011 年间在西班牙 33 家医院进行的三项观察性和前瞻性研究的临床数据。记录肿瘤反应、无进展生存期(PFS)和总生存期(OS)以及主要的舒尼替尼相关毒性。

结果

分析了 224 例患者。中位 PFS 为 10.6 个月(95%CI:9.02-12.25),中位 OS 为 21.9 个月(95%CI:17.2-26.6)。客观缓解率(ORR)为 43.8%(95%CI:36.8-50.7)。PR 的中位时间为 3.8 个月(95%CI:3.86-5.99),CR 为 8.2 个月(95%CI:4.75-9.77)。最常见的≥3 级不良事件为乏力/疲劳(18.7%)、手足综合征(6.2%)、高血压(5.8%)和中性粒细胞减少(4.8%)。在多变量分析中,手足综合征、腹泻和黏膜炎被确认为 PFS 和/或 OS 的独立预测因素(p<0.05)。

结论

舒尼替尼在日常临床实践中的疗效与临床试验相似。舒尼替尼对晚期 RCC 患者可能具有长期获益,但必须对毒性进行适当管理,以使患者能够继续接受治疗。

相似文献

1
Experience with Sunitinib in metastatic renal cell carcinoma (mRCC) patients: pooled analysis from 3 Spanish observational prospective studies.舒尼替尼治疗转移性肾细胞癌(mRCC)患者的经验:来自西班牙 3 项观察性前瞻性研究的汇总分析。
Expert Opin Drug Saf. 2018 Jun;17(6):573-579. doi: 10.1080/14740338.2017.1330410. Epub 2017 Aug 28.
2
[Comparison of efficacy between sorafenib and sunitinib as first-line therapy for metastatic renal cell carcinoma and analyze prognostic factors for survival].索拉非尼与舒尼替尼作为转移性肾细胞癌一线治疗的疗效比较及生存预后因素分析
Zhonghua Zhong Liu Za Zhi. 2018 May 23;40(5):384-389. doi: 10.3760/cma.j.issn.0253-3766.2018.05.012.
3
Phase II study of sunitinib administered in a continuous once-daily dosing regimen in patients with cytokine-refractory metastatic renal cell carcinoma.舒尼替尼每日一次持续给药方案用于细胞因子难治性转移性肾细胞癌患者的II期研究。
J Clin Oncol. 2009 Sep 1;27(25):4068-75. doi: 10.1200/JCO.2008.20.5476. Epub 2009 Aug 3.
4
Clinical Experience of Escalated Sunitinib Dose in Select Patients With Metastatic Renal Cell Carcinoma.舒尼替尼剂量递增用于部分转移性肾细胞癌患者的临床经验
Clin Genitourin Cancer. 2017 Feb;15(1):139-144. doi: 10.1016/j.clgc.2016.05.007. Epub 2016 May 27.
5
Real-life patterns of use, safety and effectiveness of sunitinib in first-line therapy of metastatic renal cell carcinoma: the SANTORIN cohort study.舒尼替尼作为转移性肾细胞癌一线治疗的实际应用模式、安全性和有效性:SANTORIN 队列研究。
Pharmacoepidemiol Drug Saf. 2017 Dec;26(12):1561-1569. doi: 10.1002/pds.4228. Epub 2017 Jun 1.
6
Hypertension as a biomarker of efficacy in patients with metastatic renal cell carcinoma treated with sunitinib.高血压作为舒尼替尼治疗转移性肾细胞癌患者疗效的生物标志物。
J Natl Cancer Inst. 2011 May 4;103(9):763-73. doi: 10.1093/jnci/djr128. Epub 2011 Apr 28.
7
Pazopanib versus sunitinib for the treatment of metastatic renal cell carcinoma patients with poor-risk features.帕唑帕尼与舒尼替尼治疗具有高风险特征的转移性肾细胞癌患者的疗效比较
Cancer Chemother Pharmacol. 2016 Aug;78(2):325-32. doi: 10.1007/s00280-016-3093-8. Epub 2016 Jun 21.
8
Sunitinib-induced hypertension, neutropaenia and thrombocytopaenia as predictors of good prognosis in patients with metastatic renal cell carcinoma.舒尼替尼引起的高血压、中性粒细胞减少和血小板减少作为转移性肾细胞癌患者预后良好的预测指标。
BJU Int. 2016 Jan;117(1):110-7. doi: 10.1111/bju.12940. Epub 2015 Jun 2.
9
Phase II trial of continuous once-daily dosing of sunitinib as first-line treatment in patients with metastatic renal cell carcinoma.舒尼替尼作为转移性肾细胞癌一线治疗药物的每日一次连续给药的 II 期临床试验。
Cancer. 2012 Mar 1;118(5):1252-9. doi: 10.1002/cncr.26440. Epub 2011 Sep 6.
10
Antitumor activity and biomarker analysis of sunitinib in patients with bevacizumab-refractory metastatic renal cell carcinoma.舒尼替尼在贝伐单抗难治性转移性肾细胞癌患者中的抗肿瘤活性及生物标志物分析
J Clin Oncol. 2008 Aug 1;26(22):3743-8. doi: 10.1200/JCO.2007.15.5416.

引用本文的文献

1
The Current and Evolving Landscape of First-Line Treatments for Advanced Renal Cell Carcinoma.晚期肾细胞癌一线治疗的现状与进展。
Oncologist. 2019 Mar;24(3):338-348. doi: 10.1634/theoncologist.2018-0267. Epub 2018 Aug 29.
2
Preclinical pharmacokinetics, interspecies scaling, and pharmacokinetics of a Phase I clinical trial of TTAC-0001, a fully human monoclonal antibody against vascular endothelial growth factor 2.TTAC-0001(一种抗血管内皮生长因子2的全人源单克隆抗体)的临床前药代动力学、种间缩放及I期临床试验药代动力学
Drug Des Devel Ther. 2018 Mar 8;12:495-504. doi: 10.2147/DDDT.S150241. eCollection 2018.