Characteristic | n |
Sex | |
Male | 63 (56%) |
Female | 49 (44%) |
Mean age (y) | 62 (range, 30–84) |
Site of primary tumor | |
Lung carcinoid | 9 (8%) |
NET of unknown primary site origin | 23 (21%) |
Gastric NET | 1 (1%) |
Small intestinal NET | 49 (44%) |
Pancreatic NET | 19 (17%) |
NET originated from cecum/appendix | 6 (5%) |
NET originated from the rectum | 2 (1.5%) |
NET originated from extrahepatic biliary tract | 2 (1.5%) |
NET originated from the esophagus | 1 (1%) |
Functional status | |
Nonfunctioning | 72 (64%) |
Functioning | 40 (36%) |
Carcinoid syndrome | 35 (31%) |
Gastrinoma | 4 (3.6%) |
Glucagonoma | 1 (0.9%) |
Grade (World Health Organization)* | |
Low-grade (G1) Ki-67, ≤2% | 31 (28%) |
Intermediate-grade (G2) Ki-67, 3%–20% | 70 (62%) |
High-grade (G3) Ki-67, >20% | 9 (8%) |
Ki-67 index not available | 2 (2%) |
Primary removed? | |
Yes | 52 (46%) |
No | 60 (54%) |
Previous treatment | |
Somatostatin analogs | 35 (31%) |
Surgery | 56 (50%) |
Chemotherapy | 40 (36%) |
Interferon α | 47 (42%) |
Radio frequency ablation (liver metastases) | 7 (6%) |
External radiation therapy | 2 (2%) |
Hepatic artery chemoembolization | 7 (6%) |
Peptide receptor radionuclide therapy | 18 (16%) |
↵* Lung carcinoids all had mitotic counts ≤ 10 and were accordingly placed in G1 or G2 groups.