Frontiers in Oncology (Nov 2024)

Case report: Tracing in parallel the salivary and gut microbiota profiles to assist Larotrectinib anticancer treatment for NTRK fusion–positive glioblastoma

  • Luigia Turco,
  • Rosa Della Monica,
  • Rosa Della Monica,
  • Pasqualina Giordano,
  • Mariella Cuomo,
  • Mariella Cuomo,
  • Manuele Biazzo,
  • Baptiste Mateu,
  • Baptiste Mateu,
  • Raimondo Di Liello,
  • Bruno Daniele,
  • Nicola Normanno,
  • Antonella De Luca,
  • Anna Maria Rachiglio,
  • Carmela Chiaramonte,
  • Francesca Maria Giugliano,
  • Lorenzo Chiariotti,
  • Lorenzo Chiariotti,
  • Lorenzo Chiariotti,
  • Giuseppe Catapano,
  • Lorena Coretti,
  • Lorena Coretti,
  • Francesca Lembo,
  • Francesca Lembo

DOI
https://doi.org/10.3389/fonc.2024.1458990
Journal volume & issue
Vol. 14

Abstract

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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 (NTRK) 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 16S 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 Enterococcus faecium, E. hirae, Akkermansia muciniphila, Barnesiella intestinihominis, and Bacteroides fragilis. 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.

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