...
【24h】

Efficacy and toxicity of sunitinib in patients with metastatic renal cell carcinoma with renal insufficiency

机译:舒尼替尼在转移性肾细胞癌合并肾功能不全患者中的疗效和毒性

获取原文
获取原文并翻译 | 示例
           

摘要

Background Patients with metastatic renal cell carcinoma (mRCC) with renal insufficiency are generally excluded from clinical trials, despite their increasing numbers. Thus, we evaluated the efficacy and toxicity of sunitinib in such patients. Patients and methods Korean patients with mRCC with renal insufficiency who had received sunitinib as first-line treatment between January 2008 and May 2012 were included. Patient characteristics, clinical outcomes and toxicities were evaluated. Overall survival (OS) and progression-free survival (PFS) were determined according to the degree of renal impairment. Results The median age of the 34 patients evaluated was 66 years, 90% had an Eastern Cooperative Oncology Group performance status of 0 or 1 and the median glomerular filtration rate was 46.5 mL min-1·1.73 m -2 (range, 21.1-59.5). The starting sunitinib dose was 37.5 and 50 mg for 12 and 22 patients, respectively. A 4-weeks-on-2-weeks-off regimen was followed for 31 patients; a 2-weeks-on-2-weeks-off regimen, for one patient; and a daily regimen, for two patients. The best response was partial response in eight patients and stable disease in 12. Median OS and PFS times were 26.3 months (95% confidence interval [CI]: 17.1-35.3) and 12.2 months (95% CI: 10.2-13.2), respectively. Common non-haematologic adverse events (AEs) were stomatitis, rash, general oedema and fatigue. The most common AEs of ≥grade 3 severity were fatigue, neutropenia and thrombocytopenia. Conclusions In patients with mRCC with renal insufficiency, sunitinib was efficacious and did not cause increased toxicity. Thus, clinicians should not hesitate to treat patients with mRCC with renal insufficiency with sunitinib.
机译:背景尽管患有肾功能不全的转移性肾细胞癌(mRCC)患者的人数不断增加,但通常仍被排除在临床试验之外。因此,我们评估了舒尼替尼在此类患者中的疗效和毒性。纳入2008年1月至2012年5月间接受舒尼替尼作为一线治疗的韩国mRCC肾功能不全患者。评估患者的特征,临床结局和毒性。根据肾功能不全的程度确定总生存期(OS)和无进展生存期(PFS)。结果评估的34例患者的中位年龄为66岁,东部合作肿瘤小组的工作状态为0或1为90%,肾小球滤过率的中位值为46.5 mL min-1·1.73 m -2(范围21.1-59.5) )。舒尼替尼的起始剂量分别为12和22位患者,分别为37.5和50 mg。 31例患者接受了4周2周疗程。一名患者接受2周2周关闭方案;和每日治疗,适用于两名患者。最好的反应是8位患者的部分反应和12位疾病的稳定。中位OS和PFS时间分别为26.3个月(95%置信区间[CI]:17.1-35.3)和12.2个月(95%CI:10.2-13.2) 。常见的非血液学不良事件(AEs)为口腔炎,皮疹,全身水肿和疲劳。 ≥3级严重程度最常见的AE是疲劳,中性粒细胞减少和血小板减少。结论对于患有肾功能不全的mRCC患者,舒尼替尼是有效的,并且不会引起毒性增加。因此,临床医生应毫不犹豫地用舒尼替尼治疗肾功能不全的mRCC患者。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号