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益生菌预防癌症治疗引起的胃肠道毒性:一项解释性综述及行动呼吁。

Probiotics to prevent gastrointestinal toxicity from cancer therapy: an interpretive review and call to action.

作者信息

Ciorba Matthew A, Hallemeier Christopher L, Stenson William F, Parikh Parag J

机构信息

aDivision of Gastroenterology, Washington University in St. Louis School of Medicine, St. Louis, Missouri bDepartment of Radiation Oncology, Mayo Clinic, Rochester, Minnesota cDepartment of Radiation Oncology, Washington University in St. Louis School of Medicine, St. Louis, Missouri, USA.

出版信息

Curr Opin Support Palliat Care. 2015 Jun;9(2):157-62. doi: 10.1097/SPC.0000000000000134.

Abstract

PURPOSE OF REVIEW

There is currently an unmet need for agents that can prevent the gastrointestinal toxicity (mucositis and enteritis) associated with chemotherapy and radiation therapy of abdominal and pelvic cancers. Herein we provide an overview of how manipulation of the gut microbiota by probiotic administration affects these gastrointestinal symptoms. We focus this review on published human trials and also provide suggestions on how the field can move forward.

RECENT FINDINGS

Several clinical trials of varying design, patient populations and probiotic products have been reported. Lactobacillus probiotics of adequate dosage demonstrate a potential to reduce gastrointestinal toxicity when administered prophylactically. Common study limitations prevent the widespread adoption of this practice at this point but are informative for rational design of future trials.

SUMMARY

No single probiotic strain or product has emerged from human clinical trials for this indication. Further human studies are required to address limitations in the current literature. Preclinical model data should be used to inform the rational design of these new clinical trials to adequately address this important question.

摘要

综述目的

目前,对于能够预防与腹部和盆腔癌症化疗及放疗相关的胃肠道毒性(粘膜炎和肠炎)的药物存在未满足的需求。在此,我们概述了通过给予益生菌来操纵肠道微生物群如何影响这些胃肠道症状。我们将本综述聚焦于已发表的人体试验,并就该领域如何向前发展提供建议。

最新发现

已经报道了几项设计、患者群体和益生菌产品各不相同的临床试验。适当剂量的乳酸杆菌益生菌在预防性给药时显示出降低胃肠道毒性的潜力。目前常见的研究局限性阻碍了这种做法的广泛采用,但对未来试验的合理设计具有参考价值。

总结

在针对该适应症的人体临床试验中,尚未出现单一的益生菌菌株或产品。需要进一步的人体研究来解决当前文献中的局限性。临床前模型数据应用于为这些新临床试验的合理设计提供信息,以充分解决这个重要问题。

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