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接受舒尼替尼治疗的癌症患者发生致命不良事件的风险。

Risk of fatal adverse events in cancer patients treated with sunitinib.

机构信息

The Second Affiliated Hospital & Yuying Children's Hospital, Wenzhou Medical University, Wenzhou, 325027, China.

The Third Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.

出版信息

Crit Rev Oncol Hematol. 2019 May;137:115-122. doi: 10.1016/j.critrevonc.2019.03.007. Epub 2019 Mar 16.

Abstract

Sunitinib, a tyrosine kinase inhibitor, is widely used in several malignancies. However, the association between sunitinib administration and fatal adverse events (FAEs) is not completely clear. Here, to calculate the overall incidence and relative risks (RRs) of FAE induced by sunitinib, PubMed and Embase were searched from inception to September 2017 for phase III randomized controlled trials (RCTs). A total of 7470 patients with a variety of solid tumors from 12 trials were included in this study. The overall incidence of FAEs with sunitinib was 1.2% (95% CI: 0.7%-1.8%). Compared with control, the addition of sunitinib significantly increased the risk of FAEs (RR, 2.34; 95% CI, 1.34-4.09; P < 0.001). Trial sequential analysis demonstrated the cumulative z curve crossed the trial sequential monitoring boundary, established sufficient and conclusive evidence. Accordingly, further studies were unlikely to alter this conclusion. The association between sunitinib and FAEs varied significantly with treatment duration or treatment strategy, but not with tumor types or sunitinib dosage. The most common causes of FAEs was hemorrhage (26.9%). In conclusion, the use of sunitinib was associated with an increased risk of FAEs in patients with solid tumors.

摘要

舒尼替尼是一种酪氨酸激酶抑制剂,广泛用于多种恶性肿瘤。然而,舒尼替尼给药与致死性不良事件(FAEs)之间的关联尚不完全清楚。在这里,为了计算舒尼替尼引起的 FAEs 的总体发生率和相对风险(RR),从 2017 年 9 月开始,我们在 PubMed 和 Embase 上搜索了 III 期随机对照试验(RCTs)。共有来自 12 项试验的 7470 名患有各种实体瘤的患者纳入本研究。舒尼替尼引起的 FAEs 的总体发生率为 1.2%(95%CI:0.7%-1.8%)。与对照组相比,舒尼替尼的添加显著增加了 FAEs 的风险(RR,2.34;95%CI,1.34-4.09;P<0.001)。试验序贯分析表明,累积 z 曲线越过了试验序贯监测边界,确立了充分和确凿的证据。因此,进一步的研究不太可能改变这一结论。舒尼替尼与 FAEs 的关联随治疗持续时间或治疗策略而显著变化,但与肿瘤类型或舒尼替尼剂量无关。FAEs 的最常见原因是出血(26.9%)。总之,舒尼替尼的使用与实体瘤患者 FAEs 的风险增加相关。

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