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1.
Eur J Clin Pharmacol ; 78(4): 687-690, 2022 Apr.
Article de Anglais | MEDLINE | ID: mdl-34993569

RÉSUMÉ

PURPOSE: Pembrolizumab is a humanized monoclonal antibody that binds to the programmed cell-death protein-1 (PD-1) on immune T-cells, thus blocking PD-1 activity. Pembrolizumab is indicated for the treatment of advanced melanoma, metastatic non-small-cell lung cancer, and head and neck squamous cell carcinoma. However, it is associated with immune-related adverse events. METHODS: We investigated the association between pembrolizumab and immune-mediated necrotizing myopathy (IMNM). We analyzed reports in the World Health Organization's global individual case safety report database, Vigibase, up to January 2020 with the MedDRA lower level term "IMNM." The association between exposure to pembrolizumab and occurrence of the adverse event was estimated by disproportionality analysis. The reporting odds ratio (ROR) was calculated with 95% confidence intervals (CIs). We analyzed the criteria of diagnosis of the adverse reaction. RESULTS: Five-hundred sixty-seven notifications were identified as IMNM of which 14 with pembrolizumab. The ROR was 17.59 (95% CI: 9.4-32.9). CONCLUSION: The diagnosis of IMNM does not always take into account recent criteria for the diagnosis of this pathology. This study highlights the existence of a signal, as well as the need for collaboration between oncologists and neurologists for these neurological pathologies.


Sujet(s)
Carcinome pulmonaire non à petites cellules , Tumeurs du poumon , Maladies musculaires , Anticorps monoclonaux humanisés/effets indésirables , Carcinome pulmonaire non à petites cellules/traitement médicamenteux , Carcinome pulmonaire non à petites cellules/anatomopathologie , Humains , Tumeurs du poumon/traitement médicamenteux , Tumeurs du poumon/anatomopathologie , Maladies musculaires/induit chimiquement
3.
Support Care Cancer ; 27(9): 3179-3182, 2019 Sep.
Article de Anglais | MEDLINE | ID: mdl-31102054

RÉSUMÉ

This study was undertaken to assess the previously unevaluated safety and feasibility of oxaliplatin-desensitization procedure add a French ambulatory cancer unit, which is a current topic in oncology. Our findings demonstrated that oxaliplatin-desensitization was safe and feasible in our ambulatory cancer unit. In routine practice, all these procedures are done on an inpatient basis starting at least the day before. Those results could change oncological practices in France and improve patients' quality of life and lower costs associated with inpatient administration.


Sujet(s)
Désensibilisation immunologique/méthodes , Hypersensibilité médicamenteuse/thérapie , Oxaliplatine/effets indésirables , Oxaliplatine/immunologie , Adulte , Sujet âgé , Sujet âgé de 80 ans ou plus , Femelle , France , Tumeurs gastro-intestinales/traitement médicamenteux , Hospitalisation , Humains , Patients hospitalisés , Mâle , Oncologie médicale , Adulte d'âge moyen , Tumeurs , Patients en consultation externe , Oxaliplatine/usage thérapeutique , Qualité de vie , Études rétrospectives
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