Literature DB >> 17419245

Prognosis of gastrointestinal stromal tumors.

Matteo Bertin1, Imerio Angriman, Marco Scarpa, Roberto Mencarelli, Riccardo Ranzato, Cesare Ruffolo, Lino Polese, Maurizio Iacobone, Davide F D'Amico.   

Abstract

BACKGROUND/AIMS: Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors (GIMT) of the gut. The aim of this retrospective study is to correlate the histological risk factors with the survival of our patients operated for GIST.
METHODOLOGY: In our department, from 1980 to October 2003, 15 patients were operated for GIST. Their mean age was 58 years old and 8 of them were males; 10 (67%) were localized in the stomach and 5 (33%) in the small bowel. In 7 cases liver metastases were present at laparotomy and 4 of them also had peritoneal diffusion. We performed immunohistochemistry for c-Kit, SMA and S100p. Mitotic index (MI) and size neoplasm were the main pathological criteria for malignity. The patients with c-kit (CD117) positive neoplasms were divided according to NIH Consensus Conference risk class, MI, tumor size, localization, SMA or S100p presence, liver metastasis and peritoneal metastasis to compare the different 5-year survival rates. Survival analysis was performed using Kaplan-Meier method and log-rank test and a p < 0.05 was considered as significant.
RESULTS: Global survival rate after 5 years was 40% and the mortality was, in all cases, due to GIST. In our experience gender, age, tumor size, localization and S100p positivity did not play any role in predicting the prognosis of GIST. On the contrary high MI and SMA positivity are significantly associated to a lower survival rate (33% vs. 86% and 39% vs. 100% at 5 years, respectively). Finally patients with metastases at laparotomy have a significantly lower 5-year survival rate (hepatic 29% vs. 100%, hepatic and peritoneal 25% us. 78%).
CONCLUSIONS: In our experience high MI and in some cases SMA expression can be considered assessed risk factors. On the other hand, criteria of benign behavior did not completely predict the long-term clinical outcome.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17419245

Source DB:  PubMed          Journal:  Hepatogastroenterology        ISSN: 0172-6390


  3 in total

1.  Skp2 expression is associated with high risk and elevated Ki67 expression in gastrointestinal stromal tumours.

Authors:  Dolores Di Vizio; Francesca Demichelis; Sara Simonetti; Guido Pettinato; Luigi Terracciano; Luigi Tornillo; Michael R Freeman; Luigi Insabato
Journal:  BMC Cancer       Date:  2008-05-13       Impact factor: 4.430

2.  Two staging systems for gastrointestinal stromal tumors in the stomach: which is better?

Authors:  Chul Hong Park; Gwang Ha Kim; Bong Eun Lee; Geun Am Song; Do Youn Park; Kyung Un Choi; Dae Hwan Kim; Tae Yong Jeon
Journal:  BMC Gastroenterol       Date:  2017-12-06       Impact factor: 3.067

3.  Clinicopathological characteristics and prognostic factors of gastrointestinal stromal tumors in Chinese patients.

Authors:  Ming-Lei Yang; Jun-Cheng Wang; Wen-Bin Zou; Ding-Kang Yao
Journal:  Oncol Lett       Date:  2018-08-17       Impact factor: 2.967

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.