TY - JOUR
T1 - Clinicopathologic Characteristics of Gastroenteropancreatic Neuroendocrine Tumors
T2 - Experience of a National Referral Hospital in Indonesia
AU - Stephanie, Marini
AU - Rahadiani, Nur
AU - Maulahela, Hasan
AU - Syaiful, Ridho Ardhi
AU - Handjari, Diah Rini
AU - Krisnuhoni, Ening
N1 - Funding Information:
This study was funded by Universitas Indonesia under PUTI grant scheme, contract number BA-886 year 2020.
Publisher Copyright:
© 2022 Marini Stephanie, Nur Rahadiani, Hasan Maulahela, Ridho Ardhi Syaiful, Diah Rini Handjari, Ening Krisnuhoni.
PY - 2022
Y1 - 2022
N2 - BACKGROUND: Gastroenteropancreatic neuroendocrine tumors (GEP-NETs) have variable biological behavior although they are all malignant. AIM: This study aimed to present the 10-year prevalence along with the clinicopathologic characteristics of GEP-NETs and their association with tumor grade at a national referral hospital in Indonesia. METHODS: This is a retrospective cross-sectional study of patients with GEP-NET who presented to Cipto Mangunkusumo Hospital from 2009 to 2019. We performed a total sampling of all available subjects by extracting list of patients with possible GEP-NET diagnosis using ICD-O code for topography and morphology. Cases were included in the study if histomorphological findings were indicative of GEP-NET and if the diagnosis was confirmed by immunohistochemistry staining. Patients with incomplete data from the hospital medical records or with missing tissue slides were excluded from the study. Clinical characteristics included age, sex, primary site, tumor stage, metastasis, hormone status, and chief complaints. Pathological characteristics included the type of GEP-NET, specimen type, grade, and presence of lymphovascular invasion (LVI). Statistical analysis was performed to determine the association between characteristics and tumor grade. RESULTS: A total of 84 cases of GEP-NET from 2009 to 2019 were included in the study; of these, 38.1% were NETs, 28.6% were neuroendocrine carcinomas, and 33.3% were mixed neuroendocrine-non-neuroendocrine neoplasm. The mean patient age was 48.36 years, and the male-to-female ratio was 1. GEP-NETs predominantly originated from the rectum (21.4%) and were mostly non-functioning (90.5%) with an average tumor size of 4.77 cm. Most tumors were localized (53.6%), but metastasis was found in 28.6% of cases. LVI was positive in 35.7% of cases. High-grade tumors were more common (54.3%) than low-grade tumors. High-grade tumors were associated with unknown primary sites, dissemination, LVI, and larger tumor size. CONCLUSION: GEP-NETs can arise from any site in the gastrointestinal tract and have variable clinicopathologic characteristics. Primary site, stage, LVI, and tumor size are associated with grade.
AB - BACKGROUND: Gastroenteropancreatic neuroendocrine tumors (GEP-NETs) have variable biological behavior although they are all malignant. AIM: This study aimed to present the 10-year prevalence along with the clinicopathologic characteristics of GEP-NETs and their association with tumor grade at a national referral hospital in Indonesia. METHODS: This is a retrospective cross-sectional study of patients with GEP-NET who presented to Cipto Mangunkusumo Hospital from 2009 to 2019. We performed a total sampling of all available subjects by extracting list of patients with possible GEP-NET diagnosis using ICD-O code for topography and morphology. Cases were included in the study if histomorphological findings were indicative of GEP-NET and if the diagnosis was confirmed by immunohistochemistry staining. Patients with incomplete data from the hospital medical records or with missing tissue slides were excluded from the study. Clinical characteristics included age, sex, primary site, tumor stage, metastasis, hormone status, and chief complaints. Pathological characteristics included the type of GEP-NET, specimen type, grade, and presence of lymphovascular invasion (LVI). Statistical analysis was performed to determine the association between characteristics and tumor grade. RESULTS: A total of 84 cases of GEP-NET from 2009 to 2019 were included in the study; of these, 38.1% were NETs, 28.6% were neuroendocrine carcinomas, and 33.3% were mixed neuroendocrine-non-neuroendocrine neoplasm. The mean patient age was 48.36 years, and the male-to-female ratio was 1. GEP-NETs predominantly originated from the rectum (21.4%) and were mostly non-functioning (90.5%) with an average tumor size of 4.77 cm. Most tumors were localized (53.6%), but metastasis was found in 28.6% of cases. LVI was positive in 35.7% of cases. High-grade tumors were more common (54.3%) than low-grade tumors. High-grade tumors were associated with unknown primary sites, dissemination, LVI, and larger tumor size. CONCLUSION: GEP-NETs can arise from any site in the gastrointestinal tract and have variable clinicopathologic characteristics. Primary site, stage, LVI, and tumor size are associated with grade.
KW - Characteristic
KW - Gastroenteropancreatic
KW - Indonesia
KW - Neoplasm
KW - Neuroendocrine
KW - Tumor
UR - http://www.scopus.com/inward/record.url?scp=85123679171&partnerID=8YFLogxK
U2 - 10.3889/oamjms.2022.7907
DO - 10.3889/oamjms.2022.7907
M3 - Article
AN - SCOPUS:85123679171
SN - 1857-5749
VL - 10
SP - 101
EP - 107
JO - Open Access Macedonian Journal of Medical Sciences
JF - Open Access Macedonian Journal of Medical Sciences
ER -