TY - JOUR
T1 - The Spigelman Staging System and the Risk of Duodenal and Papillary Cancer in Familial Adenomatous Polyposis
T2 - A Systematic Review and Meta-Analysis
AU - Mannucci, Alessandro
AU - Puzzono, Marta
AU - Goel, Ajay
AU - Möslein, Gabriela
AU - Balafas, Spyros
AU - Di Serio, Mariaclelia Stefania
AU - Cavestro, Giulia Martina
N1 - Copyright © 2024 by The American College of Gastroenterology.
PY - 2024/4
Y1 - 2024/4
N2 - OBJECTIVES: Individuals with familial adenomatous polyposis (FAP) have an almost 20% lifetime risk of duodenal adenocarcinoma, currently the leading cause of death in FAP. The Spigelman staging system provides guidance on the surveillance intervals and the timing of prophylactic surgery. Still, its accuracy in predicting duodenal and papillary cancer development has not been systematically evaluated. We investigated the sensitivity and cancer risk of the Spigelman stages.METHODS: We performed a systematic review on PubMed, MEDLINE, EMBASE, and Cochrane and used a random-effects model to pool effect sizes.RESULTS: After removing duplicate entries, we screened 1170 records and included 27 studies for quantitative analysis. Once duodenal polyposis reaches Spigelman stage IV, the risk of duodenal and papillary cancer increased to 25% (CI95%=12-45%). However, the sensitivity of Spigelman stage IV for these cancers was low (51%, CI95%=42-60%), especially for papillary adenocarcinoma (39%, CI95%=16-68%). We investigated the reasons behind these low values and observed that duodenal cancer risk factors included polyps >10 mm, polyp count >20, and polyps with high-grade dysplasia. Risk factors associated with papillary cancer included a papilla with high-grade dysplasia or >10 mm. The evidence on other risk factors was inconclusive.CONCLUSIONS: The current Spigelman staging system had a low sensitivity for duodenal and papillary adenocarcinoma. Two Spigelman variables (duodenal villous histology and polyp count) and the lack of papilla-specific variables likely contributed to the low sensitivity values for duodenal and papillary cancer, respectively. While clinicians may be familiar with its current form, there is an urgent need to update it.
AB - OBJECTIVES: Individuals with familial adenomatous polyposis (FAP) have an almost 20% lifetime risk of duodenal adenocarcinoma, currently the leading cause of death in FAP. The Spigelman staging system provides guidance on the surveillance intervals and the timing of prophylactic surgery. Still, its accuracy in predicting duodenal and papillary cancer development has not been systematically evaluated. We investigated the sensitivity and cancer risk of the Spigelman stages.METHODS: We performed a systematic review on PubMed, MEDLINE, EMBASE, and Cochrane and used a random-effects model to pool effect sizes.RESULTS: After removing duplicate entries, we screened 1170 records and included 27 studies for quantitative analysis. Once duodenal polyposis reaches Spigelman stage IV, the risk of duodenal and papillary cancer increased to 25% (CI95%=12-45%). However, the sensitivity of Spigelman stage IV for these cancers was low (51%, CI95%=42-60%), especially for papillary adenocarcinoma (39%, CI95%=16-68%). We investigated the reasons behind these low values and observed that duodenal cancer risk factors included polyps >10 mm, polyp count >20, and polyps with high-grade dysplasia. Risk factors associated with papillary cancer included a papilla with high-grade dysplasia or >10 mm. The evidence on other risk factors was inconclusive.CONCLUSIONS: The current Spigelman staging system had a low sensitivity for duodenal and papillary adenocarcinoma. Two Spigelman variables (duodenal villous histology and polyp count) and the lack of papilla-specific variables likely contributed to the low sensitivity values for duodenal and papillary cancer, respectively. While clinicians may be familiar with its current form, there is an urgent need to update it.
U2 - 10.14309/ajg.0000000000002688
DO - 10.14309/ajg.0000000000002688
M3 - Article
C2 - 38294150
SN - 0002-9270
VL - 119
SP - 617
EP - 624
JO - The American Journal of Gastroenterology
JF - The American Journal of Gastroenterology
IS - 4
ER -