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  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Schema
  9. External Links
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We are analyzing https://link.springer.com/article/10.1007/s00428-018-2297-1.

Title:
High immune cell score predicts improved survival in pancreatic cancer | Virchows Archiv
Description:
Increasing evidence suggests that cancer progression is strongly influenced by host immune response, which is represented by immune cell infiltrates. T-lymphocyte-based immunoscore has proved to be a prognostic factor in colon cancer, but its significance in pancreatic cancer is poorly known. Total of 108 patients operated (R0/R1) for pancreatic ductal adenocarcinoma (PDAC) (TNM stage I–II) were included in the study. Immune cell score (IS) was determined by scoring the samples from grade 0 to 4 according to the number of immune cells (CD3+ and CD8+) in tumor core and invasion margin using tissue microarrays, immunohistochemistry, and digital analysis. Tumors with microsatellite instability were identified by MLH1 immunostaining. High IS and low histological grade were significantly associated with better disease-specific survival (DSS) and overall survival (OS). The 5-year DSS rate for low, moderate, and high IS groups were 5.0, 15.2, and 33.4%, respectively (p = 0.007). The 5-year OS rate for the low, moderate, and high IS groups were 4.2, 13.4, and 31.5%, respectively (p = 0.004). In addition, IS and prognosis varied within a single TNM stage. There was no association between IS and any of the clinicopathological variables. IS was shown to be an independent prognostic factor for better DSS and OS in multivariate analysis, together with the histological grade of the tumor and perineural invasion. Five MLH1-negative tumors (4.6%) were found showing no correlation with IS. IS could be a useful prognostic marker in patients with PDAC treated by primary surgery.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Health & Fitness
  • Education
  • Science

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 8,123,028 visitors per month in the current month.

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How Does Link.springer.com Make Money? {💸}

We can't tell how the site generates income.

Earning money isn't the goal of every website; some are designed to offer support or promote social causes. People have different reasons for creating websites. This might be one such reason. Link.springer.com might be plotting its profit, but the way they're doing it isn't detectable yet.

Keywords {🔍}

pubmed, article, cancer, google, scholar, pancreatic, central, cas, immune, survival, adenocarcinoma, cell, ductal, patients, surg, research, prognostic, microsatellite, instability, wang, finland, cells, ann, score, immunoscore, access, privacy, cookies, content, analysis, high, wirta, prognosis, microenvironment, httpsdoiorg, clin, res, author, hospital, oulu, data, publish, search, virchows, pages, tahkola, mecklin, kellokumpu, tumor, dss,

Topics {✒️}

erkki-ville wirta month download article/chapter immune cell score cd4+ tumor-infiltrating lymphocytes cd8+ tumor-infiltrating lymphocytes t-lymphocyte-based immunoscore immune cell infiltrates disease-specific survival immune cell infiltration pancreatic cancer microenvironment full article pdf jukka-pekka mecklin related subjects widespread microsatellite instability mast cell count state research funding tumor-infiltrating regulatory host immune response immune microenvironment privacy choices/manage cookies pancreas cancer microenvironment pancreatic ductal adenocarcinoma pancreatic cancer—comparison resectable pancreatic cancer check access instant access long-term survival american joint committee article tahkola colorectal cancer prognosis correa de sampaio finnish cancer foundation author correspondence oulu university hospital tumor microenvironment deficient colon cancer article log european economic area microsatellite instability iacobuzio-donahue ca o'donnell-tormey worldwide task force mismatch repair-proficient american joint commission aatos erkko foundation finnish national authority conditions privacy policy independent prognostic factor invasive ductal carcinoma unknown primary abbreviations

Schema {🗺️}

WebPage:
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         headline:High immune cell score predicts improved survival in pancreatic cancer
         description:Increasing evidence suggests that cancer progression is strongly influenced by host immune response, which is represented by immune cell infiltrates. T-lymphocyte-based immunoscore has proved to be a prognostic factor in colon cancer, but its significance in pancreatic cancer is poorly known. Total of 108 patients operated (R0/R1) for pancreatic ductal adenocarcinoma (PDAC) (TNM stage I–II) were included in the study. Immune cell score (IS) was determined by scoring the samples from grade 0 to 4 according to the number of immune cells (CD3+ and CD8+) in tumor core and invasion margin using tissue microarrays, immunohistochemistry, and digital analysis. Tumors with microsatellite instability were identified by MLH1 immunostaining. High IS and low histological grade were significantly associated with better disease-specific survival (DSS) and overall survival (OS). The 5-year DSS rate for low, moderate, and high IS groups were 5.0, 15.2, and 33.4%, respectively (p = 0.007). The 5-year OS rate for the low, moderate, and high IS groups were 4.2, 13.4, and 31.5%, respectively (p = 0.004). In addition, IS and prognosis varied within a single TNM stage. There was no association between IS and any of the clinicopathological variables. IS was shown to be an independent prognostic factor for better DSS and OS in multivariate analysis, together with the histological grade of the tumor and perineural invasion. Five MLH1-negative tumors (4.6%) were found showing no correlation with IS. IS could be a useful prognostic marker in patients with PDAC treated by primary surgery.
         datePublished:2018-01-22T00:00:00Z
         dateModified:2018-01-22T00:00:00Z
         pageStart:653
         pageEnd:665
         sameAs:https://doi.org/10.1007/s00428-018-2297-1
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            Immunoscore
            Pancreatic cancer
            Microsatellite instability
            Microenvironment
            Immune cell score
            Pathology
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      headline:High immune cell score predicts improved survival in pancreatic cancer
      description:Increasing evidence suggests that cancer progression is strongly influenced by host immune response, which is represented by immune cell infiltrates. T-lymphocyte-based immunoscore has proved to be a prognostic factor in colon cancer, but its significance in pancreatic cancer is poorly known. Total of 108 patients operated (R0/R1) for pancreatic ductal adenocarcinoma (PDAC) (TNM stage I–II) were included in the study. Immune cell score (IS) was determined by scoring the samples from grade 0 to 4 according to the number of immune cells (CD3+ and CD8+) in tumor core and invasion margin using tissue microarrays, immunohistochemistry, and digital analysis. Tumors with microsatellite instability were identified by MLH1 immunostaining. High IS and low histological grade were significantly associated with better disease-specific survival (DSS) and overall survival (OS). The 5-year DSS rate for low, moderate, and high IS groups were 5.0, 15.2, and 33.4%, respectively (p = 0.007). The 5-year OS rate for the low, moderate, and high IS groups were 4.2, 13.4, and 31.5%, respectively (p = 0.004). In addition, IS and prognosis varied within a single TNM stage. There was no association between IS and any of the clinicopathological variables. IS was shown to be an independent prognostic factor for better DSS and OS in multivariate analysis, together with the histological grade of the tumor and perineural invasion. Five MLH1-negative tumors (4.6%) were found showing no correlation with IS. IS could be a useful prognostic marker in patients with PDAC treated by primary surgery.
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      dateModified:2018-01-22T00:00:00Z
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      pageEnd:665
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         Immunoscore
         Pancreatic cancer
         Microsatellite instability
         Microenvironment
         Immune cell score
         Pathology
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                     name:Department of Surgery, Central Finland Central Hospital, Jyväskylä, Finland
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                     name:Department of Education and Research, Central Finland Central Hospital and University of Eastern Finland, Jyväskylä, Finland
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                     name:Cancer and Translational Medicine Research Unit, Medical Research Center Oulu, University of Oulu and Oulu University Hospital, Oulu, Finland
                     type:PostalAddress
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         name:Department of Surgery, Central Finland Central Hospital, Jyväskylä, Finland
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         name:Department of Education and Research, Central Finland Central Hospital and University of Eastern Finland, Jyväskylä, Finland
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      address:
         name:Department of Surgery, Central Finland Central Hospital, Jyväskylä, Finland
         type:PostalAddress
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         name:Cancer and Translational Medicine Research Unit, Medical Research Center Oulu, University of Oulu and Oulu University Hospital, Oulu, Finland
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      name:Central Finland Central Hospital
      address:
         name:Department of Pathology, Central Finland Central Hospital, Jyväskylä, Finland
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            address:
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      name:Jukka-Pekka Mecklin
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               name:Department of Education and Research, Central Finland Central Hospital and University of Eastern Finland, Jyväskylä, Finland
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      name:Erkki-Ville Wirta
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               name:Department of Education and Research, Central Finland Central Hospital and University of Eastern Finland, Jyväskylä, Finland
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            name:Central Finland Central Hospital
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      name:Jan Böhm
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            address:
               name:Department of Pathology, Central Finland Central Hospital, Jyväskylä, Finland
               type:PostalAddress
            type:Organization
      name:Ilmo Kellokumpu
      affiliation:
            name:Central Finland Central Hospital
            address:
               name:Department of Surgery, Central Finland Central Hospital, Jyväskylä, Finland
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Department of Surgery, Central Finland Central Hospital, Jyväskylä, Finland
      name:Department of Education and Research, Central Finland Central Hospital and University of Eastern Finland, Jyväskylä, Finland
      name:Department of Surgery, Central Finland Central Hospital, Jyväskylä, Finland
      name:Department of Education and Research, Central Finland Central Hospital and University of Eastern Finland, Jyväskylä, Finland
      name:Department of Surgery, Central Finland Central Hospital, Jyväskylä, Finland
      name:Cancer and Translational Medicine Research Unit, Medical Research Center Oulu, University of Oulu and Oulu University Hospital, Oulu, Finland
      name:Department of Pathology, Central Finland Central Hospital, Jyväskylä, Finland
      name:Department of Surgery, Central Finland Central Hospital, Jyväskylä, Finland
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External Links {🔗}(178)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

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