Literature DB >> 35538309

Neuroendocrine neoplasms of the ovary: an analysis of clinicopathological characteristics and prognosis with a focus on histological grading.

Wu Huang1, Yiting Bao1, Xukai Luo1, Liangqing Yao1, Lei Yuan2.   

Abstract

OBJECTIVE: Ovarian neuroendocrine neoplasm is a rare and highly heterogeneous neoplasm. This study is aimed to describe its demographic and clinicopathological features and identify its prognostic factors.
METHODS: Clinical data of 399 patients diagnosed with ovarian neuroendocrine neoplasms between 2004 and 2016 in the Surveillance, Epidemiology, and End Results (SEER) database were analysed retrospectively. Survival curves were drawn using the Kaplan-Meier method, comparisons among different subgroups were evaluated using log-rank tests, and multivariate Cox regression analyses identified independent prognostic factors.
RESULTS: The five-year survival rates of patients with different histological types (carcinoid tumour, neuroendocrine carcinoma and special type of carcinoid tumour) were 25.5%, 96.1% and 75.0%, respectively (P < 0.001). Multivariate Cox analysis revealed that in carcinoid tumours, advanced FIGO stage was the only predictor. Additionally, no significant difference was observed among stages II, III and IV using the log-rank test. In neuroendocrine carcinoma, an advanced FIGO stage and high-grade differentiation were risk factors, while chemotherapy was a protective factor. Among all ovarian neuroendocrine neoplasms with a known histological differentiation status, no significant difference was observed among different histological types; only high-grade differentiation was an independent risk factor, and chemotherapy was a protective factor.
CONCLUSIONS: Patients with neuroendocrine carcinomas and carcinoid tumours of an advanced FIGO stage have a poor prognosis. Poor differentiation of neuroendocrine carcinomas indicates a short survival time, and adjuvant chemotherapy appears to be effective. Histological differentiation of ovarian neuroendocrine neoplasms is the most potent prognostic factor comparing to other known factors. Taken together, ovarian neuroendocrine neoplasms might be better classified as low- or high-grade ones rather than the currently used classification based on histological types in the future.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Carcinoid tumour; Histological grade; Neuroendocrine carcinoma; Ovarian neuroendocrine neoplasms; Prognosis; SEER database

Mesh:

Year:  2022        PMID: 35538309     DOI: 10.1007/s12020-022-03067-y

Source DB:  PubMed          Journal:  Endocrine        ISSN: 1355-008X            Impact factor:   3.925


  10 in total

Review 1.  Neuroendocrine tumours in rare sites: differences in nomenclature and diagnostics-a rare and ubiquitous histotype.

Authors:  Elia Guadagno; Gaetano De Rosa; Marialaura Del Basso De Caro
Journal:  J Clin Pathol       Date:  2016-02-25       Impact factor: 3.411

Review 2.  Gynecologic Cancer InterGroup (GCIG) consensus review for carcinoid tumors of the ovary.

Authors:  Nicholas Simon Reed; Eva Gomez-Garcia; Dolores Gallardo-Rincon; Brigitte Barrette; Klaus Baumann; Michael Friedlander; Ganessan Kichenadasse; Jae-Weon Kim; Domenica Lorusso; Mansoor Raza Mirza; Isabelle Ray-Coquard
Journal:  Int J Gynecol Cancer       Date:  2014-11       Impact factor: 3.437

3.  Goblet cell carcinoid tumors (adenocarcinoid) of the appendix.

Authors:  Christos Toumpanakis; Richard A Standish; Elora Baishnab; Mark C Winslet; Martyn E Caplin
Journal:  Dis Colon Rectum       Date:  2007-03       Impact factor: 4.585

Review 4.  Surgery on neuroendocrine tumours.

Authors:  Göran Akerström; Per Hellman
Journal:  Best Pract Res Clin Endocrinol Metab       Date:  2007-03       Impact factor: 4.690

5.  Placebo-Controlled, Double-Blind, Prospective, Randomized Study on the Effect of Octreotide LAR in the Control of Tumor Growth in Patients with Metastatic Neuroendocrine Midgut Tumors (PROMID): Results of Long-Term Survival.

Authors:  Anja Rinke; Michael Wittenberg; Carmen Schade-Brittinger; Behnaz Aminossadati; Erdmuthe Ronicke; Thomas M Gress; Hans-Helge Müller; Rudolf Arnold
Journal:  Neuroendocrinology       Date:  2016-01-06       Impact factor: 4.914

6.  A 5-decade analysis of 13,715 carcinoid tumors.

Authors:  Irvin M Modlin; Kevin D Lye; Mark Kidd
Journal:  Cancer       Date:  2003-02-15       Impact factor: 6.860

7.  Clinicopathologic characteristics and survival outcomes in neuroendocrine carcinoma of the ovary.

Authors:  Ying Zhu; Fanlong Meng; Huibin Fang; Zhigang Zhang; Liang Wang; Wei Zheng
Journal:  Int J Gynecol Cancer       Date:  2019-12-02       Impact factor: 3.437

8.  Guidelines for the management of gastroenteropancreatic neuroendocrine (including carcinoid) tumours (NETs).

Authors:  John K Ramage; A Ahmed; J Ardill; N Bax; D J Breen; M E Caplin; P Corrie; J Davar; A H Davies; V Lewington; T Meyer; J Newell-Price; G Poston; N Reed; A Rockall; W Steward; R V Thakker; C Toubanakis; J Valle; C Verbeke; A B Grossman
Journal:  Gut       Date:  2011-11-03       Impact factor: 23.059

9.  Aggressive neuroendocrine tumor of the ovary with multiple metastases treated with everolimus: A case report.

Authors:  Michiko Kaiho-Sakuma; Masafumi Toyoshima; Mika Watanabe; Asami Toki; Satomi Kameda; Takamichi Minato; Hitoshi Niikura; Nobuo Yaegashi
Journal:  Gynecol Oncol Rep       Date:  2018-01-04

10.  Pathological features, clinical presentations and prognostic factors of ovarian large cell neuroendocrine carcinoma: a case report and review of published literature.

Authors:  Xiaohang Yang; Junyu Chen; Ruiying Dong
Journal:  J Ovarian Res       Date:  2019-07-25       Impact factor: 4.234

  10 in total

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