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Diabetes Obes Metab:钠-葡萄糖共转运蛋白-2抑制剂与癌症

2019-04-12 xing.T 网络

由此可见,来自随机试验的现有数据并未表明SGLT-2i对一般恶性肿瘤,特别是膀胱癌的发病率有任何不利影响。

一些研究提高了对SGLT-2抑制剂(SGLT-2i)作用的担忧,表明膀胱癌的发病率增加,特别是对于依帕列净。近日,代谢内分泌疾病领域权威杂志Diabetes Obesity & Metabolism上发表了一篇研究文章。目前对随机试验进行荟萃分析的目的是评估SGLT-2i对恶性肿瘤和不同癌症类型的总体发病率的影响,合成持续至少一年的试验结果。 

研究人员在Medline和Embase数据库中检索了“Canaglifozin”、“Dapaglifozin”、“Empaglifozin”、“Ertuglifozin”、“Ipraglifozin”、“Tofoglifozin“或”Luseoglifozin“等关键词,收集了(持续时间>52周)将SGLT-2i与安慰剂或对照药进行比较的随机试验,截止至2018年12月1日。本荟萃分析考虑的结局是所有类型和几种位点特异性癌症(即乳腺癌肺癌肠癌、肝癌、胰腺癌、皮肤癌、前列腺癌和膀胱癌)。对于上面定义的所有结果,计算了Mantel-Haenszel比值比和95%置信区间(MH-OR,95%CI)。

该分析共确定了27项符合纳入标准的试验。检索试验分别在SGLT-2抑制剂和对照组中招募了27744名和20441名患者。分配给SGLT-2i和对照药物的患者之间所有恶性肿瘤的发生率没有差异(MH-OR为0.98 [0.77-1.24]。膀胱癌和任何其他类型癌症的发病率没有因任何SGLT-2i治疗而显著增加。

由此可见,来自随机试验的现有数据并未表明SGLT-2i对一般恶性肿瘤,特别是膀胱癌的发病率有任何不利影响。 

原始出处:

Ilaria Dicembrini,et al.Sodium‐Glucose co‐Transporter‐2 (SGLT‐2) inhibitors and cancer: A Meta‐analysis Of Randomized Controlled Trials.Diabetes Obesity & Metabolism.2019.https://onlinelibrary.wiley.com/doi/10.1111/dom.13745

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    2019-08-25 yzh409
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    2020-01-07 一闲
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    2019-12-21 jklm09
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    2019-09-13 guojianrong
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    2019-04-12 天地飞扬

    了解一下,谢谢分享!

    0

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总之,该研究结果揭示了Canagliflozin存在正比例失调的信号,Empagliflozin也一样,而Dapagliflozin只与脚趾截肢相关。该研究的分析依赖于数量有限的病例,并且存在药物警戒研究固有的偏倚。需要进一步的前瞻性数据以更好地描述不同SGLT-2抑制剂的截肢风险。

阿斯利康降糖药saxa/dapa(沙格列汀/达格列净)获欧盟CHMP支持批准,将成欧洲DPP-4i/SGLT-2i降糖药

英国制药巨头阿斯利康(AstraZeneca)糖尿病管线近日在欧盟监管方面传来喜讯,欧洲药品管理局(EMA)人用医药产品委员会(CHMP)支持批准糖尿病复方药saxa/dapa(saxagliptin/dapagliflozin,沙格列汀/达格列净),用于2型糖尿病成人患者的治疗。 saxa/dapa是由固定剂量的二肽基肽酶-4抑制剂(DPP-4i)saxagliptin(沙格列汀)和钠-葡萄糖

Diabetes Obes Metab:SGLT-2抑制剂后来者居上 长期疗效完胜DPP-4i和磺脲类

降糖药市场熙熙攘攘,但仍不断有新药问世。江湖传言,上市不久的钠葡萄糖协同转运蛋白-2(SGLT-2)抑制剂的强大降糖功能赶超众多畅销降糖药?真相是否如此呢?

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