scholarly journals P-184 Survival patterns of positive lymph node non metastatic gastric cancer in the United States

2016 ◽  
Vol 27 ◽  
pp. ii54
Author(s):  
A. Meshref ◽  
M. Mousa ◽  
M. Ramadan
2017 ◽  
Vol 85 (5) ◽  
pp. AB444
Author(s):  
Olaya Isabella Brewer Gutierrez ◽  
Alyssa Y. Choi ◽  
Peter V. Draganov ◽  
Lauren Khanna ◽  
Amrita Sethi ◽  
...  

2020 ◽  
Author(s):  
Jun He ◽  
Yingjie Xu ◽  
Peng Sun ◽  
Chen Qian ◽  
Jun Yan ◽  
...  

Abstract BackgroundCirculating tumor cells (CTCs) can be detected in peripheral blood of many malignant tumor cases, but low numbers of CTCs can be detected in peripheral blood of healthy individuals as well as patients with benign tumors. It is not known whether peripheral CTC counts differ between patients with benign gastric diseases and those with gastric cancer. It is still unknown whether peripheral CTC counts can act as a superior factor to assess the clinicopathological stage in gastric cancer.MethodsComparative analysis of preoperative peripheral CTC counts was completed in patients with gastric polyps and non-metastatic gastric cancer. Correlation analysis was carried out between peripheral CTC counts and histological differentiation types, histopathological types, depth of tumor infiltration, positive lymph node metastasis rate and tumor markers (CEA, CA19-9 and CA72-4).ResultsPatients with gastric cancer had higher CTC counts than those with gastric polyps (3.05 ± 0.48/3.2 ml vs 0.69 ± 0.17/3.2 ml, P < 0.05). Over 84.62% of the higher CTC group (≤ 1/3.2 ml) were gastric polyp patients. A significant difference was observed between lower CTC counts group (≤ 1/3.2 ml) and higher CTC counts group (> 1/3.2 ml) diagnosed with either gastric polyps or gastric cancer (X2 = 9.67, P < 0.005). Significant difference was observed between moderate differentiation and poor differentiation in gastric cancer (X2 = 2.43, P < 0.05).The tissue pathological types distributions showed no statistically difference between two CTC counts group (P>0.05). Significant CTC counts difference was observed between mucous membrane invasive group and muscular layer invasive group in gastric cancer (3.00 ± 0.33/3.2 ml vs 1.4 ± 0.4/3.2 ml, P < 0.05). No significant CTC counts difference was observed in different positive lymph node ratios groups in gastric cancer (P>0.05). CTC counts could show higher positive ratio when compared with CEA, CA19-9 and CA72-4 respectively (X2 = 34.37, X2 = 36.89, X2 = 29.72, P < 0.001) or jointly (X2 = 16.71, P < 0.001) in gastric cancer.ConclusionsPeripheral CTC counts were different between patients with gastric polyps and patients with gastric cancer. CTC counts could act as an independent factor to assess the clinicopathological stage in gastric cancer. CTC counts might be more sensitive than routine tumor markers to reflect the existence of early gastric cancer.


2014 ◽  
Vol 219 (4) ◽  
pp. e172
Author(s):  
Benjamin D. Powers ◽  
Senthil Jayarajan ◽  
Sharven Taghavi ◽  
Chetan Safi ◽  
Alliric I. Willis

2020 ◽  
Vol 38 (15_suppl) ◽  
pp. e16588-e16588
Author(s):  
Tuyen Hoang ◽  
Farshid Dayyani ◽  
Ariceli Alfaro ◽  
Jasmine Huynh ◽  
Jingran Ji ◽  
...  

e16588 Background: While gastric cancer is a leading cause of cancer-related mortality in Eastern Europe and Asia, it is less common in the United States. Recommendations regarding optimal treatment of non-metastatic gastric cancer (nmGC) with regard to type and extent of surgery, choice and sequence of chemotherapeutic agents, and use of radiation therapy vary somewhat depending on geographic location. To determine how variability in treatment practices affects patient outcomes, we conducted a retrospective study to evaluate clinical outcomes in nmGC patients treated at four high-volume academic institutions. Methods: California Cancer Registry of demographic and clinical data were collected for nmGC patients who underwent surgery with curative intent from 2010-2018. We conducted chart reviews of the patients’ electronic health records to validate clinical factors and outcomes. We performed multivariable Cox regressions to determine prognostic factors for outcomes. Results: Demographics of study cohort (n = 326): mean age 66 years; 64% male; 44% Caucasian, 35% Asian, 16% Latino. Tumor stage: 48% loco-regional (pT4 or pN1+) versus 52% localized (pT1-3, pN0). Histology: 47% intestinal, 30% diffuse, 8% mixed, 15% unknown. Surgery: number of recovered lymph nodes varied from 0 to 60 in any tumor stage. Chemotherapy: 20% neoadjuvant, 25% adjuvant, 16% perioperative, 39% none. Multimodality therapy: 44% surgery only, 31% chemotherapy, 25% chemotherapy and radiation. With a median follow-up after surgery of 6 years, 24% of patients developed recurrence and 40% had died. Compared to open surgery, laparoscopic surgeries was associated with lower lymph node recovery (median = 15 vs 19, p = .0042), which in turn was associated with a significant decrease in overall 5-year survival after adjusted for tumor stage (hazard ratio HR = 1.9, p = .0012). Timing of chemotherapy and addition of radiation therapy to chemotherapy did not confer further improvements in survival. In contrast, greater lymph node recovery plus chemotherapy were associated with improved survival in patients with loco-regional tumors (HR = 0.3, p = .0020). Conclusions: This study highlights major practice differences in the management of nmGC across providers and institutions. Further efforts should be made to standardize the use of chemotherapy and adequate recovery and assessment of lymph nodes in this patient population.


2016 ◽  
Vol 263 (2) ◽  
pp. 298-305 ◽  
Author(s):  
Jashodeep Datta ◽  
Matthew T. McMillan ◽  
Brett L. Ecker ◽  
Giorgos C. Karakousis ◽  
Ronac Mamtani ◽  
...  

2014 ◽  
Vol 75 (S 01) ◽  
Author(s):  
Kyle Chambers ◽  
Ashton Lehmann ◽  
Aaron Remenschneider ◽  
Matthew Dedmon ◽  
Bharat Yarlagadda ◽  
...  

Oncogene ◽  
2021 ◽  
Vol 40 (12) ◽  
pp. 2296-2308
Author(s):  
Mei Wang ◽  
Xinxin Zhao ◽  
Rong Qiu ◽  
Zheng Gong ◽  
Feng Huang ◽  
...  

AbstractLymph node metastasis (LNM), a common metastatic gastric-cancer (GC) route, is closely related to poor prognosis in GC patients. Bone marrow-derived mesenchymal stem cells (BM-MSCs) preferentially engraft at metastatic lesions. Whether BM-MSCs are specifically reprogrammed by LNM-derived GC cells (LNM-GCs) and incorporated into metastatic LN microenvironment to prompt GC malignant progression remains unknown. Herein, we found that LNM-GCs specifically educated BM-MSCs via secretory exosomes. Exosomal Wnt5a was identified as key protein mediating LNM-GCs education of BM-MSCs, which was verified by analysis of serum exosomes collected from GC patients with LNM. Wnt5a-enriched exosomes induced YAP dephosphorylation in BM-MSCs, whereas Wnt5a-deficient exosomes exerted the opposite effect. Inhibition of YAP signaling by verteporfin blocked LNM-GC exosome- and serum exosome-mediated reprogramming in BM-MSCs. Analysis of MSC-like cells obtained from metastatic LN tissues of GC patients (GLN-MSCs) confirmed that BM-MSCs incorporated into metastatic LN microenvironment, and that YAP activation participated in maintaining their tumor-promoting phenotype and function. Collectively, our results show that LNM-GCs specifically educated BM-MSCs via exosomal Wnt5a-elicited activation of YAP signaling. This study provides new insights into the mechanisms of LNM in GC and BM-MSC reprogramming, and will provide potential therapeutic targets and detection indicators for GC patients with LNM.


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