Turco Luigia, Della Monica Rosa, Giordano Pasqualina, Cuomo Mariella, Biazzo Manuele, Mateu Baptiste, Di Liello Raimondo, Daniele Bruno, Normanno Nicola, De Luca Antonella, Rachiglio Anna Maria, Chiaramonte Carmela, Giugliano Francesca Maria, Chiariotti Lorenzo, Catapano Giuseppe, Coretti Lorena, Lembo Francesca
Department of Precision Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
CEINGE-Advanced Biotechnologies "Franco Salvatore", Naples, Italy.
Front Oncol. 2024 Nov 20;14:1458990. doi: 10.3389/fonc.2024.1458990. eCollection 2024.
Oncotherapy can shape intestinal microbiota, which, in turn, may influence therapy effectiveness. Furthermore, microbiome signatures during treatments can be leveraged for the development of personalised therapeutic protocols in cancer treatment based on the identification of microbiota profiles as prognostic tools. Here, for the first time, the trajectory of gut and salivary microbiota in a patient treated with Larotrectinib, a targeted therapy approved for diagnosed glioblastoma multiforme neurotrophic tyrosine receptor kinase () gene fusion-positive, has been accurately investigated. We based our analyses on histological diagnosis, genomic and epigenomic profiling of tumour DNA, and faecal and salivary full-length rRNA gene sequencing. The study clearly evidenced a remodelling of the bacterial communities following 1 month of the NTRK-inhibitor treatment, at both gut and oral levels. We reported a boosting of specific bacteria also described in response to other chemotherapeutic approaches, such as , , , , and Moreover, several bacterial species were similarly modulated upon Larotrectinib in faecal and saliva samples. Our results suggest a parallel dynamism of microbiota profiles in both body matrices possibly useful to identify microbial biomarkers as contributors to precision medicine in cancer therapies.
肿瘤治疗可以塑造肠道微生物群,而肠道微生物群反过来又可能影响治疗效果。此外,基于将微生物群特征鉴定为预后工具,治疗期间的微生物组特征可用于开发癌症治疗中的个性化治疗方案。在此,首次对一名接受拉罗替尼治疗的患者的肠道和唾液微生物群轨迹进行了精确研究,拉罗替尼是一种被批准用于治疗诊断为多形性胶质母细胞瘤神经营养性酪氨酸受体激酶(NTRK)基因融合阳性的靶向治疗药物。我们的分析基于组织学诊断、肿瘤DNA的基因组和表观基因组分析,以及粪便和唾液全长16S rRNA基因测序。该研究清楚地证明,在接受NTRK抑制剂治疗1个月后,肠道和口腔水平的细菌群落均发生了重塑。我们报告了一些特定细菌的增加,这些细菌在对其他化疗方法(如奥沙利铂、氟尿嘧啶、伊立替康、顺铂和环磷酰胺)的反应中也有描述。此外,在粪便和唾液样本中,几种细菌种类在拉罗替尼治疗后受到类似的调节。我们的结果表明,两种身体基质中的微生物群特征具有平行的动态变化,这可能有助于识别微生物生物标志物,作为癌症治疗中精准医学的贡献因素。