33 research outputs found
Métastase hypophysaire d’un mélanome muté BRAF V600 : une réponse prometteuse au traitement combiné encorafenib–binimetinib
The 36% coefficient of variation for glucose proposed for separating stable and labile diabetes is clinically relevant: A continuous glucose monitoring-based study in a large population of type 1 diabetes patients
International audienc
Fulminant diabetes induced by PD-1 and PD-L1 inhibitors: what about glucose variability?
International audienc
Cytoponction thyroïdienne en technique monocouche : expérience de diagnostic rapide en un jour
250 LDL FROM PATIENTS WITH METABOLIC SYNDROME OR TYPE 2 DIABETES SHOW INCREASED LIPID PEROXIDATION AND ACTIVATE PLATELETS
The multifaceted nature of diabetes mellitus induced by checkpoint inhibitors
Immune checkpoint inhibitors (CPI) are increasingly being used in oncology, and many autoimmune side effects have been described. Diabetes mellitus (DM) has been reported in approximately 1% of subjects treated with programmed cell death-1 and programmed death ligand 1 (PD-1/PD-L1) inhibitors, alone or in association with CTLA-4 inhibitors. In the present mini-review, we aimed to describe different clinical pictures and pathophysiology associated with these forms of diabetes. Data on CPI-related DM was gathered from the largest case series in the literature and from our centre dedicated to immunotherapy complications (ImmuCare-Hospices Civils de Lyon). Most cases are acute autoimmune insulin-dependent diabetes which are similar to fulminant diabetes (extremely acute onset with concomitant near-normal HbA1c levels). Other cases, however, have a phenotype close to type 2 diabetes or appear as a decompensation of previously known type 2 diabetes. The occurrence of diabetes can also be a complication of autoimmune pancreatitis induced by CPI use. Finally, two cases of diabetes in a context of autoimmune lipoatrophy have recently been described. Regarding the wide variety of CPI-induced diabetes, the discovery of a glucose disorder under CPI should motivate specialised care for aetiological diagnosis and appropriate treatment
