Efficacy of everolimus in patients with metastatic insulinoma and refractory hypoglycemia

Archive ouverte

Bernard, Valérie | Lombard-Bohas, Catherine | Taquet, Marie-Caroline | Caroli-Bosc, François-Xavier | Ruszniewski, Philippe | Niccoli, Patricia | Guimbaud, Rosine | Chougnet, Cécile | Goichot, Bernard | Rohmer, Vincent | Borson-Chazot, Françoise | Baudin, Eric | Groupe Français Des Tumeurs Endocrines, .

Edité par CCSD ; Oxford Univ. Press -

International audience.

BACKGROUND: Refractory hypoglycemia in patients with metastatic insulinoma is an important cause of morbidity and mortality. Everolimus could be a new therapeutic option.

METHODS: Within the French Group, we conducted a retrospective, multicentric study of endocrine tumors to evaluate the time to the first recurrence of symptomatic hypoglycemia, after everolimus initiation, in patients with metastatic insulinoma and refractory hypoglycemia. Ongoing hyperglycemic medical options, tumor response, and safety information were recorded.

RESULTS: Twelve patients with metastatic insulinoma and refractory hypoglycemia who were treated with everolimus between May 2007 and June 2011 were reviewed. Everolimus (starting dose, 10 mg/day, except in one patient, 5 mg/day) was given after a median of four previous therapeutic lines. Medication aimed at normalizing blood glucose levels in 11 patients. After a median duration of 6.5 months (range 1-35+ months), median time to the first recurrence of symptomatic hypoglycemia was 6.5 months (range 0 to 35+ months). Three patients discontinued everolimus because of cardiac and/or pulmonary adverse events at 1, 1.5, and 7 months after initiation, which led to two deaths. Three patients discontinued everolimus because of tumor progression at 2, 3, and 10 months after initiation, without recurrence of hypoglycemia.

CONCLUSION: Everolimus appears to be a new effective treatment for patients with metastatic insulinoma and refractory hypoglycemia. Tolerance should be carefully monitored.

Consulter en ligne

Suggestions

Du même auteur

Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d'etude des Tumeurs Endocrines (GTE) cohort study.

Archive ouverte | Thevenon, Julien | CCSD

International audience. Multiple endocrine neoplasia syndrome type 1 (MEN1), which is secondary to mutation of the MEN1 gene, is a rare autosomal-dominant disease that predisposes mutation carriers to endocrine tumo...

Chemotherapy for Well-Differentiated Pancreatic Neuroendocrine Tumours with a Ki-67 Index ≥10%: Is There a More Effective Antitumour Regimen? A Retrospective Multicentre Study of the French Group of Endocrine Tumours (GTE)

Archive ouverte | Roquin, Guillaume | CCSD

International audience

Management of gastric neuro-endocrine tumours in a large French national cohort (GTE).

Archive ouverte | Manfredi, Sylvain | CCSD

IF 3.131. International audience. INTRODUCTION:Gastric neuro-endocrine tumours are rare. European guidelines for the management of neuro-endocrine tumours have been published in 2012. The aim of our survey was to st...

Chargement des enrichissements...