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Diarrhea Induced by Small Molecule Tyrosine Kinase Inhibitors Compared With Chemotherapy: Potential Role of the Microbiome

机译:小分子酪氨酸激酶抑制剂诱导的腹泻与化疗:微生物组的潜在作用

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Small molecule receptor tyrosine kinase inhibitors (SM-TKIs) are among a group of targeted cancer therapies, intended to be more specific to cancer cells compared with treatments, such as chemotherapy, hence reducing adverse events. Unfortunately, many patients report high levels of diarrhea, the pathogenesis of which remains under investigation. In this article, we compare the current state of knowledge of the pathogenesis of chemotherapy-induced diarrhea (CID) in comparison to SM-TKI–induced diarrhea, and investigate how a similar research approach in both areas may be beneficial. To this end, we review evidence that both treatment modalities may interact with the gut microbiome, and as such the microbiome should be investigated for its ability to reduce the risk of diarrhea.
机译:小分子受体酪氨酸激酶抑制剂(SM-TKIS)是一组靶向癌症疗法,其与癌细胞更具特异性,与化疗,例如化疗,因此减少不良事件。不幸的是,许多患者报告了高水平的腹泻,其发病机制仍在调查中。在本文中,与SM-TKI诱导的腹泻相比,我们比较了化疗诱导的腹泻(CID)发病机制的现状,并研究了这两个领域的类似研究方法可能是有益的。为此,我们审查了证据表明,两种治疗方式都可以与肠道微生物组相互作用,并且应该调查这种微生物组,以减少腹泻风险的能力。

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