Poorly differentiated gastro-entero-pancreatic neuroendocrine carcinomas: Are they really heterogeneous? Insights from the FFCD-GTE national cohort

• Published in: European journal of cancer (1990) 2017-07, Vol.79, p.158-165
• Main Authors: Walter, T, Tougeron, D, Baudin, E, Le Malicot, K, Lecomte, T, Malka, D, Hentic, O, Manfredi, S, Bonnet, I, Guimbaud, R, Coriat, R, Lepère, C, Desauw, C, Thirot-Bidault, A, Dahan, L, Roquin, G, Aparicio, T, Legoux, J.-L, Lombard-Bohas, C, Scoazec, J.-Y, Lepage, C, Cadiot, G
• Format: Article
• Language: English
• Subjects: Aged; Antineoplastic Combined Chemotherapy Protocols - therapeutic use; Cancer; Carboplatin - administration & dosage; Carcinoma, Neuroendocrine - mortality; Carcinoma, Neuroendocrine - pathology; Cell Transformation, Neoplastic - pathology; Chemotherapy; Cisplatin - administration & dosage; Cohort Studies; Cytotoxicity; Diagnosis; Disease control; Disease management; Endocrine system; Esophagus; Etoposide; Etoposide - administration & dosage; Female; Gastrointestinal cancer; Gastrointestinal Neoplasms - mortality; Gastrointestinal Neoplasms - pathology; Hematology, Oncology and Palliative Medicine; Humans; Ki67 index; L-Lactate dehydrogenase; Lactate dehydrogenase; Lactic acid; Life Sciences; Lymphocytes T; Male; Medical diagnosis; Medical prognosis; Metastases; Neoplasm Metastasis; Neuroendocrine carcinoma; Neuroendocrine tumors; Pancreas; Pancreatic cancer; Pancreatic carcinoma; Pancreatic Neoplasms - mortality; Pancreatic Neoplasms - pathology; Patients; Platinum; Prognosis; Stomach; Survival; Treatment; Tumors
• ISSN: 0959-8049; 1879-0852
• DOI: 10.1016/j.ejca.2017.04.009

Abstract Background Diagnosis and management of poorly differentiated gastro-entero-pancreatic (GEP) neuroendocrine carcinomas (NECs) remain challenging. Recent studies suggest prognostic heterogeneity. We designed within the French Group of Endocrine Tumours a prospective cohort to gain insight in the prognostic stratification and treatment of GEP-NEC. Patients and methods All patients with a diagnosis of GEP-NEC between 1st January 2010 and 31st December 2013 could be included in this national cohort. Adenoneuroendocrine tumours were excluded. Results 253 patients from 49 centres were included. Median age was 66 years. Main primary locations were pancreas (21%), colorectal (27%), oesophagus-stomach (18%); primary location was unknown in 20%. Tumours were metastatic at diagnosis in 78% of cases. Performance status (PS) at diagnosis was 0–1 in 79% of patients. Among the 147 (58%) cases reviewed by an expert pathological network, 39% were classified as small cell NEC and 61% as large cell NEC. Median Ki67 index was 75% (range, 20–100). Median overall survival was 15.6 (13.6–17.0) months. Significant adverse prognostic factors in univariate analysis were PS > 1 (hazard ratio [HR] = 2.5), metastatic disease (HR = 1.6), NSE > 2 upper limit of normal [ULN]; HR = 3.2), CgA > 2 ULN (HR = 1.7) and lactate dehydrogenase >2 ULN (HR = 2.1). After first-line palliative chemotherapy (CT1) with platinum-etoposide (n = 152), objective response, progression-free survival and overall survival were 50%, 6.2 and 11.6 months; they were 24%, 2.9 and 5.9, respectively, after post-CT1 FOLFIRI regimen (n = 72). Conclusions We report a large prospective series of GEP-NEC which show the predominance of large cell type and advanced stage at diagnosis. Prognosis was found more homogeneous than previously reported, mainly impacted by PS and tumour burden.