Prognostic Ability of Tumor Budding Outperforms Poorly Differentiated Clusters in Gastric Cancer

The prognostic value of histological phenomena tumor budding (TB) and poorly differentiated clusters (PDCs) have been less studied in gastric cancer (GAC) and the data provided so far are controversial. In our study, 290 surgically resected GAC cases were evaluated for TB according to the criteria o...

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Veröffentlicht in:Cancers 2022-09, Vol.14 (19), p.4731
Hauptverfasser: Szalai, Luca, Jakab, Ákos, Kocsmár, Ildikó, Szirtes, Ildikó, Kenessey, István, Szijártó, Attila, Schaff, Zsuzsa, Kiss, András, Lotz, Gábor, Kocsmár, Éva
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Sprache:eng
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Zusammenfassung:The prognostic value of histological phenomena tumor budding (TB) and poorly differentiated clusters (PDCs) have been less studied in gastric cancer (GAC) and the data provided so far are controversial. In our study, 290 surgically resected GAC cases were evaluated for TB according to the criteria of International Tumor Budding Consensus Conference (ITBCC) and PDC, and both parameters were scored on a three-grade scale as described for colorectal cancer previously (0: Grade0, 1-4: Grade1, 5-9: Grade2 and ≥10: Grade3) and classified as low (Grade0-2) and high (Grade3) TB/PDC. High TB/PDC was associated with diffuse-type morphology, higher pT status, incomplete surgical resection, poor tumor differentiation and perineural and lymphovascular invasion. Multivariable survival analyses have shown an independent prognostic role of high TB with poorer overall survival in the total cohort ( = 0.014) and in intestinal-type adenocarcinomas ( = 0.005). Multivariable model revealed high TB as an independent predictor for lymph node metastasis in both the total cohort ( = 0.019) and in the intestinal type adenocarcinomas ( = 0.038). In contrast to tumor budding, no significant association was found between PDC and the occurrence of lymph node metastasis and tumor stage and even survival. In conclusion, tumor budding is an independent prognostic factor of survival in gastric cancer, especially in intestinal-type adenocarcinomas.
ISSN:2072-6694
2072-6694
DOI:10.3390/cancers14194731