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Vascular endothelial growth factor ( VEGF VEGF ) antibody significantly increases the risk of hand–foot skin reaction to multikinase inhibitors ( MKI MKI s): A systematic literature review and meta‐analysis

机译:血管内皮生长因子(VEGF VEGF)抗体显着提高了对多立糖酶抑制剂的手足皮肤反应的风险(MKI MKI S):系统文献综述和荟萃分析

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Summary With the use of multikinase inhibitors ( MKI s) having emerged in recent years, skin toxicities such as hand–foot skin reaction ( HFSR ) are primary side effects, and they lack effective prediction methods. Here, we updated a previous systematic review by establishing a meta‐analysis of the risk of developing HFSR among patients receiving MKI s and antivascular endothelial growth factor antibody. Publications from PubMed and abstracts presented at the American Society of Clinical Oncology Annual Meeting up to February 5, 2015, were searched to identify relevant studies, and a total of 236 patients with metastatic tumours in nine trials were included for analysis. In the meta‐analysis, the pooled incidence rates of all‐grade and high‐grade HFSR among patients who received the combination therapy were 56.9% [95% confidence interval ( CI ), 45%‐71.1%] and 14.3% (95%? CI , 9%‐24.2%), respectively, with significant differences observed with MKI monotherapy ( P ??.05). Further subgroup analysis demonstrated that increasing the dosages of bevacizumab (77.8% vs 51.1%, P ?=?.04) and MKI s (64.3% vs 52.6%, P ?=?.02) significantly increased HFSR incidence. Moreover, combination with chemotherapy exerted a minimal effect on HFSR risk (61% vs 55.3%, P ?=?.5). This updated review and meta‐analysis confirm the increased risk of HFSR incidence due to the use of MKI s and antivascular endothelial growth factor antibody. Thus, using these therapies requires safety standards.
机译:发明内容近年来出现了多立糖酶抑制剂(MKI S),诸如手脚皮肤反应(HFSR)的皮肤毒性是初级副作用,并且它们缺乏有效的预测方法。在这里,我们通过建立患者在接受MKI S和抗病毒内皮生长因子抗体的患者中发展HFSR的风险来更新先前的系统审查。在2015年2月5日的美国临床肿瘤学会年会中发布的PubMed和Abstracts的出版物被搜查识别相关研究,共有236例患有九项试验中的转移性肿瘤患者进行分析。在荟萃分析中,接受联合治疗的患者中的所有级和高级HFSR的汇集发病率为56.9%[95%置信区间(CI),45%-71.1%]和14.3%(95%) CI,9%-24.2%)分别观察到MKI单疗法(P = 05)观察到显着差异。进一步的亚组分析证明,增加贝伐单抗的剂量(77.8%Vs 51.1%,p?=β.04)和MKIs(64.3%Vs 52.6%,p?=β.02)显着增加了HFSR发病率。此外,与化疗组合施加对HFSR风险的最小影响(61%Vs 55.3%,p?= 5)。此更新的审查和Meta-Analysis证实了由于使用MKI S和抗病毒内皮生长因子抗体而增加了HFSR发病率的风险。因此,使用这些疗法需要安全标准。

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