## Abstract In some populationβbased studies, a shorter median survival was observed in peritoneal as compared with pleural, malignant mesothelioma, but in others, longer median survival times or higher proportions of longβterm survivors were reported. Statistical instability could have caused thes
Predictors and survival of synchronous peritoneal carcinomatosis of colorectal origin: A population-based study
β Scribed by Valery E. Lemmens; Yvonne L. Klaver; Vic J. Verwaal; Harm J. Rutten; Jan Willem W. Coebergh; Ignace H. de Hingh
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- French
- Weight
- 301 KB
- Volume
- 128
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
The aim of our study was to provide populationβbased data on incidence and prognosis of synchronous peritoneal carcinomatosis and to evaluate predictors for its development. Diagnosed in 1995β2008, 18,738 cases of primary colorectal cancer were included. Predictors of peritoneal carcinomatosis were analysed by multivariable logistic regression analysis. Median survival in months was calculated by site of metastasis. In the study period, 904 patients were diagnosed with synchronous peritoneal carcinomatosis (4.8% of total, constituting 24% of patients presenting with M1 disease). The risk of peritoneal carcinomatosis was increased in case of advanced T stage [T4 vs. T1,2: odds ratio (OR) 4.7, confidence limits 4.0β5.6), advanced N stage [N0 vs. N1,2: OR 0.2 (0.1β0.2)], poor differentiation grade [OR 2.1 (1.8β2.5)], younger age [<60 years vs. 70β79 years: OR 1.4 (1.1β1.7)], mucinous adenocarcinoma [OR 2.0 (1.6β2.4)] and rightβsided localisation of primary tumour [left vs. right: OR 0.6 (0.5β0.7)]. Median survival of patients with peritoneum as single site of metastasis remained dismal [1995β2001: 7 (6β9) months; 2002β2008: 8 (6β11) months], contrasting the improvement among patients with liver metastases [1995β2001: 8 (7β9) months; 2002β2008: 12 (11β14) months]. To conclude, synchronous peritoneal metastases from colorectal cancer are more frequent among younger patients and among patients with advanced T stage, mucinous adenocarcinoma, rightβsided tumours and tumours that are poorly differentiated. The prognosis of synchronous peritoneal carcinomatosis remains poor with a median survival of 8 months and even worse if concomitant metastases in other organs are present.
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