Ghatalia Pooja, Je Youjin, Nguyen Paul L, Trinh Quoc-Dien, Choueiri Toni K, Sonpavde Guru
Department of Internal Medicine, University of Alabama at Birmingham (UAB), AL, United States.
Department of Food and Nutrition, Kyung Hee University, Seoul, Republic of Korea.
Crit Rev Oncol Hematol. 2015 Aug;95(2):251-63. doi: 10.1016/j.critrevonc.2015.03.006. Epub 2015 Apr 9.
A trial-level meta-analysis of randomized phase II/III controlled trials in renal cell carcinoma (RCC) and other malignancies was conducted to systematically determine the relative risk (RR) of fatigue, a common side effect associated with single agent therapy with vascular endothelial growth factor receptor (VEGFR) tyrosine kinase inhibitors (TKI) and mammalian target of rapamycin inhibitors (mTORi). The RR of all grade fatigue and high grade fatigue in 7304 patients from 19 trials was 1.35 (95% CI 1.22-1.49, p<0.001) and 1.33 (95% CI 0.97-1.82, p=0.08), respectively in patients receiving VEGFR TKIs or mTORi. The summary incidence of all grade and high grade fatigue in the drug arm was 38.2% (95% CI 31.8-45.1) and 4.0% (95% CI 2.8-5.7), respectively. The type of drug (VEGFR TKI vs. mTORi), line of therapy, age, type of tumor (RCC vs. others) and median duration of therapy did not affect the risk of all-grade fatigue.
我们进行了一项针对肾细胞癌(RCC)和其他恶性肿瘤的随机II/III期对照试验的试验水平荟萃分析,以系统地确定疲劳的相对风险(RR),疲劳是血管内皮生长因子受体(VEGFR)酪氨酸激酶抑制剂(TKI)和雷帕霉素靶蛋白抑制剂(mTORi)单药治疗常见的副作用。在接受VEGFR TKI或mTORi治疗的患者中,来自19项试验的7304名患者中所有级别疲劳和高级别疲劳的RR分别为1.35(95%CI 1.22-1.49,p<0.001)和1.33(95%CI 0.97-1.82,p=0.08)。药物治疗组中所有级别和高级别疲劳的汇总发生率分别为38.2%(95%CI 31.8-45.1)和4.0%(95%CI 2.8-5.7)。药物类型(VEGFR TKI与mTORi)、治疗线数、年龄、肿瘤类型(RCC与其他)和中位治疗持续时间均不影响所有级别疲劳的风险。