Abstract 2185TiP
Background
Immune checkpoint inhibitor (ICI) therapy has revolutionized cancer treatment but can cause immune related adverse events (irAEs) which we currently do not know how to prevent. These irAEs influence patients’ quality of life and oncological treatment course. The gut plays an essential role in immune homeostasis and gut dysbiosis is implicated in (auto)inflammatory conditions. The American Gut project, an international microbiome study, showed that healthy volunteers who ingested at least 30 different plants (vegetables, fruits, nuts) weekly had a more diverse microbiome than those who consumed 10 or less. A fibre-rich diet has been associated with improved outcome of ICI treatment and with reductions of perceived stress.
Trial design
The FORX trial investigates whether altering the composition of the gut microbiome can improve ICI tolerance. In our tertiary reference centre, we are supplementing the diets of solid tumour patients starting ICI with weekly boxes containing 30 different plants during the first 12 weeks of their treatment. The increased fibre intake is expected to strengthen the gut microbiome and reduce the incidence of irAEs. Stool and blood samples will clarify the microbial and cytokine signatures associated with irAEs. Baseline physical activity and body composition will be assessed given recent retrospective data showing synergistic effects of exercise, body composition and ICI therapy. Quality of life questionnaires will be completed at baseline, week 6 and week 12 throughout the intervention. The FORX trial is the first prospective trial to translate the cited retrospective findings into a concrete dietary advice. Our trial will provide valuable insights in the interaction between the gut microbiome, physical fitness and autoimmunity and serve as a basis for nutritional and probiotic advice. It will empower cancer patients and improve their quality of life.
Clinical trial identification
NCT05832606.
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
UZ Brussel.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
2172P - Development and evaluation of the usefulness of an immune-related adverse events interview application
Presenter: AKIKO YANO
Session: Poster session 07
2173P - Exploring the complex needs of older patients receiving targeted therapies and immune checkpoint inhibitors for renal and skin cancers at the Royal Marsden Hospital
Presenter: Niamh Cunningham
Session: Poster session 07
2174P - The impact of exposure to antibiotic (ATB) and proton pump inhibitor (PPI) therapy on immune checkpoint inhibitor (ICI) treatment on overall survival (OS): A population-based study
Presenter: Lawson Eng
Session: Poster session 07
2175P - Sex and age-related differences in immunotherapy-induced toxicities
Presenter: Mafalda Teixeira da Costa
Session: Poster session 07
2176P - Rechallenge of immune checkpoint inhibitors after immune-related adverse events: A systematic review
Presenter: Jin Young Kim
Session: Poster session 07
2177P - Immunotherapy adverse events association with inflammation scores: A real-world data analysis from a Portuguese hospital
Presenter: Catarina Fernandes
Session: Poster session 07
2179P - Prospective monitoring of autoimmune events in cancer immunotherapy patients: A report on the first 658 patients in the PRAISE study
Presenter: Eden Sebbag
Session: Poster session 07
2180P - Detrimental effect of an early exposure to antibiotics on the outcomes of immunotherapy in a multi-tumor cohort of patients
Presenter: Víctor Albarrán
Session: Poster session 07
2181P - Effect of different corticosteroid treatment strategies on checkpoint inhibitors pneumonitis outcomes
Presenter: Hui Guo
Session: Poster session 07
2182P - Patient involvement to improve prospective follow-up: Quality of life data after cancer immunotherapy from the PRAISE study
Presenter: Eden Sebbag
Session: Poster session 07