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The prognostic relevance of histologic subtype in appendiceal adenocarcinoma

Authors :
Felice N. van Erning
Ignace H. J. T. de Hingh
Laura M. Legué
Valery E.P.P. Lemmens
Geert-Jan Creemers
Clément J. Huysentruyt
Epidemiologie
RS: GROW - R3 - Innovative Cancer Diagnostics & Therapy
Public Health
Source :
European Journal of Surgical Oncology, 46(3), 433-438. ELSEVIER SCI LTD, European Journal of Surgical Oncology, 46(3), 433-438. W.B. Saunders
Publication Year :
2020

Abstract

BACKGROUND: The aim of this population-based study was to determine the prognostic value of the histologic subtypes mucinous (MAC), non-mucinous (AC) and signet ring cell (SRCC) adenocarcinoma among patients with appendiceal cancer.METHODS AND MATERIALS: Data from the Netherlands Cancer Registry (NCR) of patients with primary appendiceal adenocarcinomas with MAC, AC and SRCC histologic subtype, diagnosed between 2001 and 2015 were used (n = 675). To categorize patients according to the recent histopathological classification, the NCR was linked with the Dutch Pathology Registry (PALGA). Log-rank tests and Kaplan-Meier analyses were performed to estimate overall survival (OS), and the cox proportional hazards model was run to identify prognostic factors.RESULTS: AC was the most frequently encountered histologic subtype (50.9%), followed by MAC (35.8%) and SRCC (13.3%). In locoregional disease, histologic subtype was not a prognostic factor for OS with 5-year survival rates for patients with AC, MAC and SRCC of 60.0%, 60.5% and 69.6% respectively (p = 0.68). Metastatic disease was more common in SRCC (53.8%) than in MAC (38.8%) and AC (23.4%) (p CONCLUSION: Histologic subtype had no prognostic relevance in locoregional or systemic metastatic disease in appendiceal adenocarcinoma. In peritoneal metastases, mucinous histologic subtype was a favorable prognostic factor, compared to non-mucinous and signet ring cell subtype.

Details

Language :
English
ISSN :
07487983
Volume :
46
Issue :
3
Database :
OpenAIRE
Journal :
European Journal of Surgical Oncology
Accession number :
edsair.doi.dedup.....7e0b9e8355eafd4e6633024486c262e9
Full Text :
https://doi.org/10.1016/j.ejso.2019.10.018