口腔微生物组和全身抗肿瘤药物在癌症治疗中的应用:系统综述

M. E. Rodríguez-Fuentes, M. Pérez‐Sayáns, Luis Chauca-Bajaña, G. Barbeito-Castiñeiras, María Luisa Pérez del Molino-Bernal, R. López-López
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Material and Methods A systematic review was performed following the PRISMA protocol and the PICO question established was: patients diagnosed with cancer, who are candidates for receiving systemic antineoplastics (P=Patients), that undergo oral microbiome determinations (I=Intervention), before and after systemic antineoplastics administration (C=Comparison), to analyse changes in the oral microbiome composition (O=Outcome). The bibliographic search was carried out in PubMed and other scientific repositories. Results Out of 166 obtained articles, only 5 met eligibility criteria. Acute myeloid leukaemia (AML) was the most frequent type of cancer (40 %) among the participants. Only one of the studies included a control group of healthy subjects. Heterogeneity in the protocols and approaches of the included studies hindered a detailed comparison of the outcomes. However, it was stated that a decrease in bacteria α diversity is often associated with oral mucositis. 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引用次数: 1

摘要

背景口腔黏膜炎是接受全身抗肿瘤药物治疗的癌症患者最常见的副作用之一。然而,导致这种情况的潜在生物学机制仍不清楚。因此,有假设认为,全身性抗肿瘤药物可能导致口腔微生物群失衡,从而引发口腔黏膜损伤。材料和方法根据PRISMA方案进行了系统评价,建立的PICO问题是:被诊断为癌症的患者,他们是接受全身抗肿瘤药物治疗的候选人(P=患者),在全身抗肿瘤药物治疗前后进行口腔微生物组测定(I=干预)(C=比较),以分析口腔微生物组组成的变化(O=结果)。文献检索在PubMed和其他科学知识库中进行。结果获得的166篇文献中,仅有5篇符合入选标准。急性髓性白血病(AML)是参与者中最常见的癌症类型(40%)。其中只有一项研究纳入了健康受试者的对照组。纳入研究的方案和方法的异质性阻碍了对结果的详细比较。然而,有研究表明,细菌α多样性的减少通常与口腔黏膜炎有关。另一方面,真菌多样性与口腔黏膜炎无关,尽管口腔念珠菌病患者的α多样性在基线时较低。结论接受全身抗肿瘤手术患者口腔微生物变化的科学证据不足。应该进行进一步的研究,以确定可能在接受全身抗肿瘤治疗的患者口腔黏膜损伤发病机制中发挥关键作用的微生物。关键词:口腔炎,抗肿瘤药物,肿瘤,微生物群,免疫治疗
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Oral microbiome and systemic antineoplastics in cancer treatment: A systematic review
Background Oral mucositis is one of the most common side effects in cancer patients receiving systemic antineoplastics. However, the underlying biological mechanisms leading to this condition are still unclear. For this reason, it has been hypothesised that systemic antineoplastics may cause an imbalance on the oral microbiota that subsequently triggers oral mucosa damage. Material and Methods A systematic review was performed following the PRISMA protocol and the PICO question established was: patients diagnosed with cancer, who are candidates for receiving systemic antineoplastics (P=Patients), that undergo oral microbiome determinations (I=Intervention), before and after systemic antineoplastics administration (C=Comparison), to analyse changes in the oral microbiome composition (O=Outcome). The bibliographic search was carried out in PubMed and other scientific repositories. Results Out of 166 obtained articles, only 5 met eligibility criteria. Acute myeloid leukaemia (AML) was the most frequent type of cancer (40 %) among the participants. Only one of the studies included a control group of healthy subjects. Heterogeneity in the protocols and approaches of the included studies hindered a detailed comparison of the outcomes. However, it was stated that a decrease in bacteria α diversity is often associated with oral mucositis. On the other hand, fungal diversity was not associated with oral mucositis although α diversity was lower at baseline on patients developing oral candidiasis. Conclusions There is insufficient scientific evidence of oral microbiological changes in patients undergoing systemic antineoplastics. Further investigations ought to be carried out to identify microorganisms that might play a key role in the pathogenesis of oral mucosa damage in patients undergoing systemic antineoplastics. Key words:Stomatitis, antineoplastic agents, neoplasms, microbiota, immunotherapy.
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