OP0336 COMMONLY USED DRUGS IN RHEUMATOLOGY MAY ALTER ANTI-TUMORAL RESPONSE TO IMMUNE CHECKPOINT INHIBITORS
| Autor: | Thomas Barnetche, Léa Dousset, Remi Veillon, Sorilla Prey, Thierry Schaeverbeke, Nadia Mehsen-Cetre, Alain Ravaud, Marine Gross-Goupil, Amaury Daste, Marie-Elise Truchetet, Caroline Dutriaux, Marie Kostine, Julien Seneschal, Charlotte Domblides, Charlotte Vergnenegre, Christophe Richez, Eleonora Mauric, Edouard Forcade, Léa Rouxel, Marie Beylot-Barry, Bernard Bannwarth, Baptiste Sionneau |
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| Rok vydání: | 2019 |
| Předmět: |
Oncology
medicine.medical_specialty biology medicine.drug_class business.industry medicine.medical_treatment Antibiotics Cancer Retrospective cohort study Immunotherapy Gut flora medicine.disease biology.organism_classification Rheumatology Prednisone Internal medicine medicine Adverse effect business medicine.drug |
| Zdroj: | Oral Presentations. |
| DOI: | 10.1136/annrheumdis-2019-eular.7470 |
| Popis: | Background Immune checkpoint inhibitors (ICIs) are revolutionizing the treatment of some advanced cancers. Gut microbiota has emerged as an important component of anti-tumoral response and can also be related to the occurrence of immune-related adverse events (irAEs). It has recently been shown that antibiotic treatment given at the initiation of ICI therapy had a dramatic impact on microbiota that compromised the anti-tumoral effect of ICIs (1). Objectives To evaluate whether co-medications known to have a potential impact on gut microbiota may alter ICI efficacy and/or irAE occurrence when given at ICI onset. Methods This was a retrospective cohort study including all cancer patients who received ICIs at our institution from May 2015 to September 2017. Co-medications given to the patients within one month before or one month after the first administration of ICI were extracted from medical records on the basis of a predefined list of medications known to impact gut microbiota. The tumour response, occurrence of irAEs and patient outcomes were assessed on a regular basis. Overall survival (OS) has been considered from the start of ICI therapy. Results 635 patients (70% male, mean age 64.5 years) were included, of whom 293 had melanoma, 150 had advanced non-small cell lung cancer and 83 had renal carcinoma. A previous autoimmune disorder was present in 8% of patients, mainly rheumatic and endocrine diseases. Psychotropic drugs (41.1%), proton pump inhibitors (PPIs) (37.3%), angiotensin-converting enzyme (ACE) inhibitors and/or angiotensin II receptor blockers (ARBs) (32%), glucocorticoids (GC) (24.2%), antibiotics (21.4%), statins (20.8%) and morphine (20.6%) were the most co-prescribed medications. Baseline GC use, when ≥ 10mg of prednisone equivalent, was associated with a significant decrease in OS (median 4.5 months versus 24.3 months; p Conclusion As many of these treatments are used by rheumatologists, one should be aware of their potential detrimental effect when used at ICI initiation, that sometimes could have been avoided. Reference [1] Routy B et al. Gut microbiome influences efficacy of PD-1-based immunotherapy against epithelial tumors. Science. 2018 Jan 5;359(6371):91-97. Disclosure of Interests None declared |
| Databáze: | OpenAIRE |
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