Literature DB >> 31015316

Mesothelin Expression Is a Predictive Factor for Peritoneal Recurrence in Curatively Resected Stage III Gastric Cancer.

Su-Jin Shin1, Sejung Park2, Min Hwan Kim3, Chung Mo Nam4, Hyunki Kim5, Yoon Young Choi6, Min Kyu Jung3,7, Hye Jin Choi3,7, Sun Young Rha3,7, Hyun Cheol Chung8,7.   

Abstract

BACKGROUND: Mesothelin is overexpressed in many solid tumors, and recent studies have shown that mesothelin expression is associated with poor outcomes in several malignant tumors and may play a role in cancer progression. Clinical trials of mesothelin-targeted immunotherapies are currently under way, but the correlation between mesothelin expression and gastric cancer prognosis is still unclear. SUBJECTS, MATERIALS, AND METHODS: Mesothelin expression in tumor cells was evaluated immunohistochemically in 958 patients with advanced gastric cancer and interpreted according to the intensity and extent of staining. Samples were scored from 0 to 2, with high expression defined as a score of 2. Clinicopathological factors, overall survival (OS), recurrence-free survival (RFS), and sites of initial recurrence, including peritoneal recurrence, were evaluated. Staging was performed according to the American Joint Committee on Cancer 7th edition.
RESULTS: High mesothelin expression was observed in 49.7% of patients and significantly associated with high pathologic T (p = .021) and peritoneal recurrence (p = .018). Multivariate survival analysis showed that high mesothelin expression was independently associated with poor RFS (p = .001), OS (p = .001), and peritoneal recurrence (p = .002) in addition to stage, lymphovascular invasion, and Lauren classification. In a subgroup analysis of peritoneal recurrence, high mesothelin expression was also an independent prognostic factor in stage III (p = .013) and diffuse/mixed type gastric cancer (p = .010).
CONCLUSION: High mesothelin expression is correlated with poor outcomes. In addition, mesothelin expression, Lauren classification, and stage are meaningful predictive factors for peritoneal recurrence. Moreover, mesothelin was a significant predictor of a high risk of peritoneal recurrence in patients with stage III gastric cancer. IMPLICATIONS FOR PRACTICE: This study demonstrates that high mesothelin expression correlates with poor outcomes and is a significant predictor of peritoneal recurrence in patients with stage III gastric cancer. This study provides instrumental evidence for designing anti-mesothelin antibody-drug conjugate clinical trials in patients with diffuse-type gastric cancer to reduce their high risk of peritoneal carcinomatosis. © AlphaMed Press 2019.

Entities:  

Keywords:  Mesothelin; Peritoneal recurrence; Prediction; Stomach cancer; Survival

Mesh:

Substances:

Year:  2019        PMID: 31015316      PMCID: PMC6853112          DOI: 10.1634/theoncologist.2018-0896

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  31 in total

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2.  Survival model predictive accuracy and ROC curves.

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Journal:  Clin Cancer Res       Date:  2012-02-27       Impact factor: 12.531

5.  Phase II clinical trial of postoperative S-1 monotherapy for gastric cancer patients with free intraperitoneal cancer cells detected by real-time RT-PCR.

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6.  Lauren Histologic Type Is the Most Important Factor Associated With Pattern of Recurrence Following Resection of Gastric Adenocarcinoma.

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8.  Binding of ovarian cancer antigen CA125/MUC16 to mesothelin mediates cell adhesion.

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9.  Mesothelin expression in triple negative breast carcinomas correlates significantly with basal-like phenotype, distant metastases and decreased survival.

Authors:  Gary Tozbikian; Edi Brogi; Kyuichi Kadota; Jeffrey Catalano; Muzaffar Akram; Sujata Patil; Alice Y Ho; Jorge S Reis-Filho; Britta Weigelt; Larry Norton; Prasad S Adusumilli; Hannah Yong Wen
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10.  Mesothelin binding to CA125/MUC16 promotes pancreatic cancer cell motility and invasion via MMP-7 activation.

Authors:  Shih-Hsun Chen; Wei-Chien Hung; Pu Wang; Colin Paul; Konstantinos Konstantopoulos
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Review 7.  Gastric cancer: An epigenetic view.

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