PS02.225: PROGNOSTIC VALUE OF LYMPH NODE METASTASIS IN DIFFERENT SITES IN PATHOLOGICAL T3 ESOPHAGEAL SQUAMOUS CELL CARCINOMA PATIENTS

2018 ◽  
Vol 31 (Supplement_1) ◽  
pp. 185-186
Author(s):  
Ying-Jian Wang ◽  
Kun-Kun Li ◽  
Xue-Hai Liu ◽  
Wei Guo

Abstract Background The aim of this study was to evaluate the impact of different sites of lymph node metastasis in pathological T3 (pT3) esophageal squamous cell carcinoma patients (ESCC). Methods We retrospectively reviewed 300 consecutive ESCC patients who underwent radical minimally invasive esophagectomy (MIE) and two-field lymphadenectomy from 2010 to 2015. After exclusion, 111 cases were analyzed. Patients were divided into 3 groups (mediastinal metastasis, abdominal metastasis, and simultaneous metastasis) according to their lymph node metastatic sites. Disease-free survival (DFS) and disease-specific survival (DSS) were analyzed. Results The results showed that the incidence of lymph node metastasize to mediastinum, abdomen, and simultaneous was 55 (49.5%), 21(18.9%), 35(31.6%), respectively. Patients in simultaneous metastasis group had a higher cancer recurrence (log-rank test; P = 0.0341; Figure 1A) than mediastinum and abdomen metastasis group. Similarly, patients in simultaneous metastasis group had greater rate of cancer-related death (log-rank test; P = 0.0177; Figure 1B) than mediastinum and abdomen metastasis group. In the multivariate model, metastasis site was an independent risk factor in both DFS (P = 0.0402; HR, 1.4071; 95% CI, 1.0171–1.9466) and DSS (P = 0.0238; HR, 1.4342; 95% CI, 1.0507–1.9577). Conclusion Simultaneous mediastinal and abdominal lymph node metastasis is associate with a relatively poor prognosis in pT3 ESCC patients. Disclosure All authors have declared no conflicts of interest.

BMC Cancer ◽  
2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Xiaofeng Duan ◽  
Xiaobin Shang ◽  
Jie Yue ◽  
Zhao Ma ◽  
Chuangui Chen ◽  
...  

Abstract Background A nomogram was developed to predict lymph node metastasis (LNM) for patients with early-stage esophageal squamous cell carcinoma (ESCC). Methods We used the clinical data of ESCC patients with pathological T1 stage disease who underwent surgery from January 2011 to June 2018 to develop a nomogram model. Multivariable logistic regression was used to confirm the risk factors for variable selection. The risk of LNM was stratified based on the nomogram model. The nomogram was validated by an independent cohort which included early ESCC patients underwent esophagectomy between July 2018 and December 2019. Results Of the 223 patients, 36 (16.1%) patients had LNM. The following three variables were confirmed as LNM risk factors and were included in the nomogram model: tumor differentiation (odds ratio [OR] = 3.776, 95% confidence interval [CI] 1.515–9.360, p = 0.004), depth of tumor invasion (OR = 3.124, 95% CI 1.146–8.511, p = 0.026), and tumor size (OR = 2.420, 95% CI 1.070–5.473, p = 0.034). The C-index was 0.810 (95% CI 0.742–0.895) in the derivation cohort (223 patients) and 0.830 (95% CI 0.763–0.902) in the validation cohort (80 patients). Conclusions A validated nomogram can predict the risk of LNM via risk stratification. It could be used to assist in the decision-making process to determine which patients should undergo esophagectomy and for which patients with a low risk of LNM, curative endoscopic resection would be sufficient.


2008 ◽  
Vol 23 (4) ◽  
pp. 619-625 ◽  
Author(s):  
Dong Uk Kim ◽  
Jun Haeng Lee ◽  
Byung-Hoon Min ◽  
Sang Goon Shim ◽  
Dong Kyung Chang ◽  
...  

2010 ◽  
Vol 286 (12) ◽  
pp. 10725-10734 ◽  
Author(s):  
Zhao-li Chen ◽  
Xiao-hong Zhao ◽  
Ji-wen Wang ◽  
Bao-zhong Li ◽  
Zhen Wang ◽  
...  

microRNAs (miRNAs) regulate gene expression at the post-transcriptional level and play important roles in tumor initiation and progression. Recently, we examined the global miRNA expression profile of esophageal squamous cell carcinoma (ESCC) and demonstrated that miR-92a was highly expressed in tumor tissues. In this study, we found that the up-regulation of miR-92a was significantly correlated with the status of lymph node metastasis and TNM stage in 107 ESCC patients. Moreover, the up-regulation of miR-92a was associated with poor survival of ESCC patients and might be used as an independent prognostic factor. Next, we investigated the role and mechanism of miR-92a in ESCC cells, and found that miR-92a modulated the migration and invasion but not apoptosis and proliferation of ESCC cells in vitro. We further demonstrated that miR-92a directly targeted the CDH1 3′-UTR and repressed the expression of CDH1, a tumor metastasis suppressor. In addition, restoring of miR-92a-resistant CDH1 expression in miR-92a-overexpression cells recovered the pro-metastasis activity of miR-92a. Taken together, we demonstrated that miR-92a promotes ESCC cell migration and invasion at least partially via suppression of CDH1 expression, and patients with up-regulated miR-92a are prone to lymph node metastasis and thus have poor prognosis.


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