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Targeted therapy-induced diarrhea: A review of the literature

机译:针对性治疗引起的腹泻:文献综述

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Purpose of research: Revision of the literature on targeted therapy-induced diarrhea (TT-ID). Principal results: TT-ID is frequent; the mechanisms are mainly secretive, followed by ischemic or autoimmune ones. The duration of TT-ID is protracted over time. Its intensity is of grade G1-G3 but may be fatal in patients with diffuse colitis or on ipilimumab. However, no specific guidelines are available on management of different grades of TT-ID. Preventive measures with antibiotics, probiotics or activated charcoal should be further investigated. Loperamide is the first choice drug followed by octreotide. The role of corticosteroids is controversial. Conclusion: Early assessment and management of TT-ID is essential to prevent the worsening of this side-effect, patients' hospitalization and dose reduction or oncological treatment discontinuation. Future research is needed to better understand the pathophysiological mechanisms of TT-ID and it should also be investigated whether a specific pharmacological and/or non pharmachological approach is indicated.
机译:研究目的:修订靶向治疗引起的腹泻(TT-ID)文献。主要结果:TT-ID频繁;其机制主要是分泌性的,其次是缺血性或自身免疫性的。 TT-ID的持续时间会随着时间延长。它的强度为G1-G3级,但对于弥漫性结肠炎或依普利单抗患者可能致命。但是,没有针对不同等级的TT-ID的管理的特定指南。应进一步研究使用抗生素,益生菌或活性炭的预防措施。洛哌丁胺是首选药物,其次是奥曲肽。皮质类固醇的作用是有争议的。结论:TT-ID的早期评估和管理对于防止这种副作用的恶化,患者的住院和减少剂量或肿瘤治疗的中止至关重要。需要进行进一步的研究以更好地理解TT-ID的病理生理机制,并且还应研究是否应指明一种特定的药理学和/或非药理学方法。

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