Characteristics and treatment options of glucagonomas: a national study from the French Group of Endocrine Tumors and ENDOCAN-RENATEN network

Author:

Perrier Marine1ORCID,Brugel Mathias1,Gérard Laura2,Goichot Bernard3,Lièvre Astrid4,Lepage Come5,Hautefeuille Vincent6,Do Cao Christine7,Smith Denis8,Thuillier Philippe9,Cros Jérôme10,Cadiot Guillaume1,Walter Thomas2,de Mestier Louis11

Affiliation:

1. Reims-Champagne-Ardenne University, Department of Hepato-Gastroenterology and Digestive Oncology, Robert Debré Hospital , Reims 51100 , France

2. Department of Digestive Oncology, ENETS Centre of Excellence, Hospices Civils de Lyon , Lyon 69003 , France

3. Department of Endocrinology, Diabetology & Nutrition, Hôpital Hautepierre, Strasbourg University Hospital, Strasbourg 67200 , France

4. Department of Gastroenterology, Pontchaillou University Hospital, Rennes University, INSERM U1242 , Rennes 35000 , France

5. Federation Francophone de Cancérologie Digestive (FFCD), EPICAD INSERM LNC-UMR 1231, University of Burgundy and Franche Comté , Dijon 21000 , France

6. Department of Hepato-Gastroenterology and Digestive Oncology, Amiens University Hospital , Amiens 80480 , France

7. Department of Endocrinology, Hôpital Claude Huriez, Lille University Hospital , Lille 59000 , France

8. Department of Hepato-Gastroenterology and Digestive Oncology, Haut-Lévêque Hospital, Bordeaux University Hospital , Pessac 33600 , France

9. Department of Endocrinology, University Hospital of Brest , Brest 29200 , France

10. Université Paris-Cité, Department of Pathology, ENETS Centre of Excellence, Beaujon Hospital (APHP.Nord) , Clichy 92110 , France

11. Université Paris-Cité, Department of Pancreatology and Digestive Oncology, ENETS Centre of Excellence, Beaujon Hospital (APHP.Nord) , Clichy 92110 , France

Abstract

Abstract Objective Glucagonoma is a very rare functional pancreatic neuroendocrine tumor (PanNET). We aimed to provide data on the diagnosis, prognosis, and management of patients with glucagonoma. Design and Methods In this retrospective national cohort, we included all patients with glucagonoma, defined by at least 1 major criterion (necrolytic migratory erythema [NME] and/or recent-onset diabetes, and/or weight loss ≥ 5 kg) associated with either glucagonemia > 2 × upper limit of normal or positive glucagon immunostaining. Antisecretory efficacy was defined as partial/complete resolution of glucagonoma symptoms. Antitumor efficacy was assessed according to the time to next treatment (TTNT). Results Thirty-eight patients were included with median age 58.7 yo, primary PanNET located in the tail (68.4%), synchronous metastases (63.2%). Median Ki-67 index was 3%. Most frequent glucagonoma symptoms at diagnosis were NME (86.8%), weight loss (68.4%), and diabetes (50%). Surgery of the primary PanNET was performed in 76.3% of cases, mainly with curative intent (61.5%). After surgery, complete resolution of NME was seen in 93.8% (n = 15/16). The secretory response rates were 85.7%, 85.7%, 75%, and 60% with surgery of metastases (n = 6/7), chemotherapy (n = 6/7), liver-directed therapy (n = 6/8), and somatostatin analogs (n = 6/10), respectively. All lines combined, longer TTNT was reported with chemotherapy (20.2 months). Median overall survival (OS) was 17.3 years. The Ki-67 index > 3% was associated with shorter OS (hazard ratio 5.27, 95% CI [1.11-24.96], P = .036). Conclusion Patients with glucagonoma had prolonged survival, even in the presence of metastases at diagnosis. Curative-intent surgery should always be considered. Chemotherapy, peptide receptor radionuclide therapy, or liver-directed therapy seems to provide both substantial antitumor and antisecretory efficacies.

Funder

French Group of Endocrine Tumors

IPSEN-pharma

Publisher

Oxford University Press (OUP)

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

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