본문 바로가기
KERD
논문KCI 등재

Gastric Neuroendocrine Tumors According to the 2019 World Health Organization Grading System: A Single-Center, Retrospective Study

2

조회

0

다운로드

0

인용

0

참고문헌

키워드

초록

Background/Aims: Although gastric neuroendocrine tumors (NETs) are uncommon neoplasms, their prevalence is increasing. The clinical importance of the World Health Organization (WHO) classification of gastric NETs, compared with NETs in other organs, has been underestimated. This study aimed to systematically evaluate the clinical and pathologic characteristics of gastric NETs based on the 2019 WHO classification and to assess the survival outcomes of patients from a single-center with a long-term follow-up. Methods: The medical records of 427 patients with gastric NETs who underwent endoscopic or surgical resection between January 2000 and March 2020 were retrospectively reviewed. All specimens were reclassified according to the 2019 WHO classification. The clinicopathologic characteristics, treatment, and oncologic outcomes of 139 gastric NETs were analyzed. Results: The patients’ median age was 53.0 years (interquartile range [IQR], 46.0 to 63.0 years). The median follow-up period was 36.0 months (IQR, 15.0 to 63.0 months). Of the patients, 92, 44, and 3 had grades 1, 2, and 3 NETs, respectively. The mean tumor size significantly increased as the tumor grade increased (p=0.025). Patients with grades 2 and 3 gastric NETs more frequently had lymphovascular invasion (29.8% vs 10.9%, p=0.005) and deeper tissue invasion (8.5% vs 0%, p=0.012) than those with grade 1 tumors. The overall disease-specific survival rate was 100%. Two patients with grades 2-3 gastric NETs experienced extragastric recurrence. Conclusions: Although gastric NETs have an excellent prognosis, grade 2 or grade 3 gastric NETs are associated with a larger size, deeper invasion, and extragastric recurrence, which require active treatment.

Abstract

Background/Aims: Although gastric neuroendocrine tumors (NETs) are uncommon neoplasms, their prevalence is increasing. The clinical importance of the World Health Organization (WHO) classification of gastric NETs, compared with NETs in other organs, has been underestimated. This study aimed to systematically evaluate the clinical and pathologic characteristics of gastric NETs based on the 2019 WHO classification and to assess the survival outcomes of patients from a single-center with a long-term follow-up. Methods: The medical records of 427 patients with gastric NETs who underwent endoscopic or surgical resection between January 2000 and March 2020 were retrospectively reviewed. All specimens were reclassified according to the 2019 WHO classification. The clinicopathologic characteristics, treatment, and oncologic outcomes of 139 gastric NETs were analyzed. Results: The patients’ median age was 53.0 years (interquartile range [IQR], 46.0 to 63.0 years). The median follow-up period was 36.0 months (IQR, 15.0 to 63.0 months). Of the patients, 92, 44, and 3 had grades 1, 2, and 3 NETs, respectively. The mean tumor size significantly increased as the tumor grade increased (p=0.025). Patients with grades 2 and 3 gastric NETs more frequently had lymphovascular invasion (29.8% vs 10.9%, p=0.005) and deeper tissue invasion (8.5% vs 0%, p=0.012) than those with grade 1 tumors. The overall disease-specific survival rate was 100%. Two patients with grades 2-3 gastric NETs experienced extragastric recurrence. Conclusions: Although gastric NETs have an excellent prognosis, grade 2 or grade 3 gastric NETs are associated with a larger size, deeper invasion, and extragastric recurrence, which require active treatment.

참고문헌 (43)

  1. Oberndorfer S, "Karzinoide tumoren des dunndarms", Frankfurt Z Path, 1, pp.426~432 (1907)
  2. Lawrence B, "A clinical perspective on gastric neuroendocrine neoplasia", Curr Gastroenterol Rep, 13, pp.101~109 (2011)
  3. Modlin IM, "Gastrointestinal carcinoids : the evolution of diagnostic strategies", J Clin Gastroenterol, 40, pp.572~582 (2006)
  4. Basuroy R, "Review article : the investigation and management of gastric neuroendocrine tumours", Aliment Pharmacol Ther, 39, pp.1071~1084 (2014)
  5. Niederle MB, "Gastroenteropancreatic neuroendocrine tumours : the current incidence and staging based on the WHO and European Neuroendocrine Tumour Society classification : an analysis based on prospectively collected parameters", Endocr Relat Cancer, 17, pp.909~918 (2010)
  6. Klöppel G, "The gastroenteropancreatic neuroendocrine cell system and its tumors : the WHO classification", Ann N Y Acad Sci, 1014, pp.13~27 (2004)
  7. Sato Y, "Management of gastric and duodenal neuroendocrine tumors", World J Gastroenterol, 22, pp.6817~6828 (2016)
  8. Rindi G, "Three subtypes of gastric argyrophil carcinoid and the gastric neuroendocrine carcinoma : a clinicopathologic study", Gastroenterology, 104, pp.994~1006 (1993)
  9. La Rosa S, "Histologic characterization and improved prognostic evaluation of 209 gastric neuroendocrine neoplasms", Hum Pathol, 42, pp.1373~1384 (2011)
  10. Christopoulos C, "Gastric neuroendocrine tumors : biology and management", Ann Gastroenterol, 18, pp.127~140 (2005)
  11. Nagtegaal ID, "The 2019 WHO classification of tumours of the digestive system", Histopathology, 76, pp.182~188 (2020)
  12. Ji-Yeon Mun, "A 13-year experience with gastric neuroendocrine tumors: A single institute study", 대한종양외과학회지, 14(1), pp.8~14 (2018), 대한종양외과학회[DOI]
  13. Yang Z, "Gastric neuroendocrine tumors(G-Nets) : incidence, prognosis and recent trend toward improved survival", Cell Physiol Biochem, 45, pp.389~396 (2018)
  14. Roberto GA, "Gastric neuroendocrine tumor : a practical literature review", World J Gastrointest Oncol, 12, pp.850~856 (2020)
  15. Kimura K, "An endoscopic recognition of the atrophic border and its significance in chronic gastritis", Endoscopy, 1, pp.87~97 (1969)
  16. Warren S, "Multiple primary malignant tumors : a survey of the literature and a statistical study", Am J Cancer, 16, pp.1358~1414 (1932)
  17. Cockburn AN, "Neuroendocrine proliferations of the stomach : a pragmatic approach for the perplexed pathologist", Adv Anat Pathol, 20, pp.148~157 (2013)
  18. Amin MB, "AJCC cancer staging manual" (2018), Springer International Publishing
  19. Hallet J, "Exploring the rising incidence of neuroendocrine tumors : a population-based analysis of epidemiology, metastatic presentation, and outcomes", Cancer, 121, pp.589~597 (2015)
  20. Yao JC, "One hundred years after"carcinoid" : epidemiology of and prognostic factors for neuroendocrine tumors in 35, 825 cases in the United States", J Clin Oncol, 26, pp.3063~3072 (2008)
  21. Dasari A, "Trends in the incidence, prevalence, and survival outcomes in patients with neuroendocrine tumors in the United States", JAMA Oncol, 3, pp.1335~1342 (2017)
  22. Frilling A, "Neuroendocrine tumor disease : an evolving landscape", Endocr Relat Cancer, 19, pp.R163~R185 (2012)
  23. Cives M, "Gastroenteropancreatic neuroendocrine tumors", CA Cancer J Clin, 68, pp.471~487 (2018)
  24. Dacha S, "Hypergastrinemia", Gastroenterol Rep(Oxf), 3, pp.201~208 (2015)
  25. Lundell L, "Systematic review : the effects of long-term proton pump inhibitor use on serum gastrin levels and gastric histology", Aliment Pharmacol Ther, 42, pp.649~663 (2015)
  26. Butler OL, "Frequency and causes of false-positive elevated plasma concentrations of fasting gut hormones in a specialist neuroendocrine tumor center", Front Endocrinol(Lausanne), 11, pp.606264~ (2020)
  27. Rindi G, "The 2010 WHO classification of digestive neuroendocrine neoplasms : a critical appraisal four years after its introduction", Endocr Pathol, 25, pp.186~192 (2014)
  28. Garcia-Carbonero R, "Incidence, patterns of care and prognostic factors for outcome of gastroenteropancreatic neuroendocrine tumors(GEP-NETs) : results from the National Cancer Registry of Spain(RGETNE)", Ann Oncol, 21, pp.1794~1803 (2010)
  29. Gluckman CR, "Gastric neuroendocrine tumors(carcinoids)", Curr Gastroenterol Rep, 21, pp.13~ (2019)
  30. Chung CS, "Clinical features and outcomes of gastric neuroendocrine tumors after endoscopic diagnosis and treatment: a Digestive Endoscopy Society of Tawian (DEST)", Medicine(Baltimore), 97, pp.e12101~ (2018)
  31. Pape UF, "Management of followup of neuroendocrine neoplasias", Best Pract Res Clin Endocrinol Metab, 30, pp.129~140 (2016)
  32. Kulke MH, "Neuroendocrine tumors, version 1. 2015", J Natl Compr Canc Netw, 13, pp.78~108 (2015)
  33. Delle Fave G, "ENETS consensus guidelines for the management of patients with gastroduodenal neoplasms", Neuroendocrinology, 95, pp.74~87 (2012)
  34. Jun Liong Chin, "Diagnosis and Management of Upper Gastrointestinal Neuroendocrine Tumors", Clinical Endoscopy, 50(6), pp.520~529 (2017), 대한소화기내시경학회
  35. Bosman FT, "WHO classification of tumours of the digestive system", World Health Organization, ~ (2010)
  36. Lloyd RV, "WHO classification of tumours of endocrine organs", International Agency for Research on Cancer, ~ (2017)
  37. Sato Y, "Management and clinical outcomes of type I gastric carcinoid patients : retrospective, multicenter study in Japan", Dig Endosc, 26, pp.377~384 (2014)
  38. Merola E, "Type I gastric carcinoids : a prospective study on endoscopic management and recurrence rate", Neuroendocrinology, 95, pp.207~213 (2012)
  39. Uygun A, "Long-term results of endoscopic resection for type I gastric neuroendocrine tumors", J Surg Oncol, 109, pp.71~74 (2014)
  40. Jung JH, "Risk factors of lymph node metastasis in patients with gastric neuroendocrine tumor with normal serum gastrin level", Hepatogastroenterology, 62, pp.207~213 (2015)
  41. Scoazec JY, "Well-differentiated grade 3 digestive neuroendocrine tumors: myth or reality? The PRONET study group", J Clin Oncol, 30(15_Suppl), pp.4129~ (2012)
  42. Scoazec JY, "Professional practices and diagnostic issues in neuroendocrine tumour pathology : results of a prospective one-year survey among French pathologists(the PRONET study)", Neuroendocrinology, 105, pp.67~76 (2017)
  43. Pellat A, "Well differentiated grade 3 neuroendocrine tumors of the digestive tract : a narrative review", J Clin Med, 9, pp.1677~ (2020)

관련 논문AI추천

Clinical Characteristics and Long-term Outcomes of Gastric Neuroendocrine TumorsCho Soo-Jeong, Chung Hyunsoo, Kim Jiyoon, Kim Sang Gyun, Zheng Quanxin거트앤리버 소화기연관학회협의회 · Gut and Liver2025 · 제19권 제2호Proposal for a Standardized Pathology Report of Gastroenteropancreatic Neuroendocrine Tumors: Prognostic Significance of Pathological Parameters강대영, 강윤경, 김경미, 김미정, 김우호, 김윤화, 김준미, 김현기, 손진희, 정은선, 조미연, 진소영, 최은희, 최준혁대한병리학회 · Journal of Pathology and Translational Medicine2013 · 제47권 제3호Gastroenteropancreatic Neuroendocrine Tumors with Liver Metastases in Korea: A Clinicopathological Analysis of 72 Cases in a Single Institute김경미, 박영석, 박철근, 신유주, 이보람, 이지연, 장기택, 하상윤, 현지연대한암학회 · Cancer Research and Treatment2015 · 제47권 제4호Incidence and clinical characteristics of gastroenteropancreatic neuroendocrine tumor in Korea: a single-center experience김상우, 김진수, 노상영, 박재명, 이명아, 이인석, 임철현, 전병연, 조유경, 최명규대한내과학회 · The Korean Journal of Internal Medicine2017 · 제32권 제3호Risk Factors for Lymph Node Metastasis and Oncologic Outcomes in Small Rectal Neuroendocrine Tumors with Lymphovascular Invasion남승주, Chang Hee Jin, Jeon Han Ho, Kim Byung Chang, Kim Junho, Kim Su Young거트앤리버 소화기연관학회협의회 · Gut and Liver2022 · 제16권 제2호Current Trends of the Incidence and Pathological Diagnosis of Gastroenteropancreatic Neuroendocrine Tumors (GEP-NETs) in Korea 2000-2009: Multicenter Study주미, 강대영, 강미선, 강윤경, 구미진, 국명철, 김경미, 김미정, 김수진, 김우호, 김윤화, 김준미, 김현기, 김희경, 문우성, 박도윤, 박문일, 배한익, 손진희, 윤선오, 이재혁, 장세진, 장희경, 정은선, 조미연, 조창호, 진소영, 최준혁대한암학회 · Cancer Research and Treatment2012 · 제44권 제3호

이 간행물의 다른 논문 (14건)