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  2. Matching Content Categories
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We are analyzing https://link.springer.com/article/10.1007/s10585-015-9697-2.

Title:
Pattern of metastasis and outcome in patients with breast cancer | Clinical & Experimental Metastasis
Description:
There is growing evidence about differences in metastatic spread among breast cancer (BC) biologic subtypes (BS). Aim of this study was to analyze the pattern of metastasization according to BS and to explore the corresponding prognosis. A series of 544 consecutive patients receiving anticancer therapy for metastatic BC from 2004 to 2013, was analyzed. BS were defined by immunohistochemistry according to St Gallen 2013 criteria. Association between BS and the different distant localizations was analyzed. Prognosis was described in terms of overall survival (OS), progression free survival (PFS) and post progression survival (PPS). Results were reported taking luminal A BC as reference. Triple negative BC showed a higher tropism for lung (OR 4.30 95 % CI 1.41–13.1), while non luminal HER2 subtype was associated with a higher rate of liver metastases (OR 3.61 95 % CI 1.36–9.58). All subtypes were associated with a lower risk of bone-only localization. Central nervous system (CNS) involvement was more common in HER2 positive BC (OR 6.3, 95 % CI 1.08–36.66). Liver, lung and CNS involvement influenced negatively OS (HR 1.64, 95 % CI 1.29–2.07; HR 1.49, 95 % CI 1.18–1.90; HR 2.891, 95 % CI 1.85–4.51, respectively) and PFS (HR 1.39, 95 % CI 1.13–1.71; HR 1.26, 95 % CI 1.02–1.55; HR 1.75, 95 % CI 1.12–2.71, respectively). Multivariate analysis confirmed liver involvement as independent predictor of worse OS (HR 1.64, 95 % CI 1.15–2.34). Stratification by metastatic pattern showed significant differences in terms of PPS but not in terms of PFS. The study suggests that BS may be characterized by typical patterns of metastatic spread and have different impact on clinical outcome.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Health & Fitness
  • Education
  • Science

Content Management System {πŸ“}

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 {πŸ“ˆ}

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 7,626,432 visitors per month in the current month.

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How Does Link.springer.com Make Money? {πŸ’Έ}

We can't see how the site brings in money.

Websites don't always need to be profitable; some serve as platforms for education or personal expression. Websites can serve multiple purposes. And this might be one of them. Link.springer.com could be secretly minting cash, but we can't detect the process.

Keywords {πŸ”}

cancer, breast, article, pubmed, google, scholar, metastatic, cas, metastasis, patients, oncol, outcome, subtypes, central, clin, gerratana, puglisi, metastases, access, privacy, cookies, content, clinical, survival, patterns, treatment, publish, research, search, pattern, bonotto, spread, study, prognosis, terms, liver, risk, rev, author, udine, data, information, log, journal, january, fanotto, minisini, explore, differences, distant,

Topics {βœ’οΈ}

month download article/chapter her2-overexpressing breast cancer early-stage breast cancer central nervous system lymph node-negative disease full article pdf metastatic breast cancer her2 positive bc privacy choices/manage cookies early breast cancer prognostic factors relapsed breast cancer breast cancer classification clinical parameters influencing estrogen receptor status breast cancer subtypes luminal her2 subtype global cancer statistics breast cancer patients clin exp metastasis nationwide cohort study european economic area scope submit manuscript reported taking luminal protein expression predict real-world scenario breast conservation treatment conditions privacy policy metastatic spread bone metastasis article log progression free survival post progression survival accepting optional cookies liver metastases risk factors loco-regional treatment immunohistochemically defined luminal breast cancer article cite clinical outcome journal finder publish prognostic significance author information authors article gerratana distant metastases check access instant access measures metastatic bc

Questions {❓}

  • Puglisi F, Fontanella C, Numico G et al (2014) Follow-up of patients with early breast cancer: is it time to rewrite the story?

Schema {πŸ—ΊοΈ}

WebPage:
      mainEntity:
         headline:Pattern of metastasis and outcome in patients with breast cancer
         description:There is growing evidence about differences in metastatic spread among breast cancer (BC) biologic subtypes (BS). Aim of this study was to analyze the pattern of metastasization according to BS and to explore the corresponding prognosis. A series of 544 consecutive patients receiving anticancer therapy for metastatic BC from 2004 to 2013, was analyzed. BS were defined by immunohistochemistry according to St Gallen 2013 criteria. Association between BS and the different distant localizations was analyzed. Prognosis was described in terms of overall survival (OS), progression free survival (PFS) and post progression survival (PPS). Results were reported taking luminal A BC as reference. Triple negative BC showed a higher tropism for lung (OR 4.30 95Β % CI 1.41–13.1), while non luminal HER2 subtype was associated with a higher rate of liver metastases (OR 3.61 95Β % CI 1.36–9.58). All subtypes were associated with a lower risk of bone-only localization. Central nervous system (CNS) involvement was more common in HER2 positive BC (OR 6.3, 95Β % CI 1.08–36.66). Liver, lung and CNS involvement influenced negatively OS (HR 1.64, 95Β % CI 1.29–2.07; HR 1.49, 95Β % CI 1.18–1.90; HR 2.891, 95Β % CI 1.85–4.51, respectively) and PFS (HR 1.39, 95Β % CI 1.13–1.71; HR 1.26, 95Β % CI 1.02–1.55; HR 1.75, 95Β % CI 1.12–2.71, respectively). Multivariate analysis confirmed liver involvement as independent predictor of worse OS (HR 1.64, 95Β % CI 1.15–2.34). Stratification by metastatic pattern showed significant differences in terms of PPS but not in terms of PFS. The study suggests that BS may be characterized by typical patterns of metastatic spread and have different impact on clinical outcome.
         datePublished:2015-01-29T00:00:00Z
         dateModified:2015-01-29T00:00:00Z
         pageStart:125
         pageEnd:133
         sameAs:https://doi.org/10.1007/s10585-015-9697-2
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            Immunophenotype
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            Prognostic factors
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            Hematology
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                        type:PostalAddress
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                        name:Department of Medical and Biological Sciences, University of Udine, Udine, Italy
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ScholarlyArticle:
      headline:Pattern of metastasis and outcome in patients with breast cancer
      description:There is growing evidence about differences in metastatic spread among breast cancer (BC) biologic subtypes (BS). Aim of this study was to analyze the pattern of metastasization according to BS and to explore the corresponding prognosis. A series of 544 consecutive patients receiving anticancer therapy for metastatic BC from 2004 to 2013, was analyzed. BS were defined by immunohistochemistry according to St Gallen 2013 criteria. Association between BS and the different distant localizations was analyzed. Prognosis was described in terms of overall survival (OS), progression free survival (PFS) and post progression survival (PPS). Results were reported taking luminal A BC as reference. Triple negative BC showed a higher tropism for lung (OR 4.30 95Β % CI 1.41–13.1), while non luminal HER2 subtype was associated with a higher rate of liver metastases (OR 3.61 95Β % CI 1.36–9.58). All subtypes were associated with a lower risk of bone-only localization. Central nervous system (CNS) involvement was more common in HER2 positive BC (OR 6.3, 95Β % CI 1.08–36.66). Liver, lung and CNS involvement influenced negatively OS (HR 1.64, 95Β % CI 1.29–2.07; HR 1.49, 95Β % CI 1.18–1.90; HR 2.891, 95Β % CI 1.85–4.51, respectively) and PFS (HR 1.39, 95Β % CI 1.13–1.71; HR 1.26, 95Β % CI 1.02–1.55; HR 1.75, 95Β % CI 1.12–2.71, respectively). Multivariate analysis confirmed liver involvement as independent predictor of worse OS (HR 1.64, 95Β % CI 1.15–2.34). Stratification by metastatic pattern showed significant differences in terms of PPS but not in terms of PFS. The study suggests that BS may be characterized by typical patterns of metastatic spread and have different impact on clinical outcome.
      datePublished:2015-01-29T00:00:00Z
      dateModified:2015-01-29T00:00:00Z
      pageStart:125
      pageEnd:133
      sameAs:https://doi.org/10.1007/s10585-015-9697-2
      keywords:
         Breast neoplasm
         Immunophenotype
         Metastatic spread
         Prognostic factors
         Outcome measures
         Cancer Research
         Biomedicine
         general
         Oncology
         Hematology
         Surgical Oncology
      image:
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1007%2Fs10585-015-9697-2/MediaObjects/10585_2015_9697_Fig1_HTML.gif
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                     name:Department of Oncology, University Hospital of Udine, Udine, Italy
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                  name:University of Udine
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                     name:Department of Medical and Biological Sciences, University of Udine, Udine, Italy
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                     type:PostalAddress
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                  name:University Hospital of Udine
                  address:
                     name:Department of Oncology, University Hospital of Udine, Udine, Italy
                     type:PostalAddress
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            name:S. Bolzonello
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                     name:Department of Oncology, University Hospital of Udine, Udine, Italy
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                  name:University Hospital of Udine
                  address:
                     name:Department of Oncology, University Hospital of Udine, Udine, Italy
                     type:PostalAddress
                  type:Organization
            type:Person
            name:G. Fasola
            affiliation:
                  name:University Hospital of Udine
                  address:
                     name:Department of Oncology, University Hospital of Udine, Udine, Italy
                     type:PostalAddress
                  type:Organization
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            name:F. Puglisi
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                  name:University Hospital of Udine
                  address:
                     name:Department of Oncology, University Hospital of Udine, Udine, Italy
                     type:PostalAddress
                  type:Organization
                  name:University of Udine
                  address:
                     name:Department of Medical and Biological Sciences, University of Udine, Udine, Italy
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      name:Springer Netherlands
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         name:Department of Medical and Biological Sciences, University of Udine, Udine, Italy
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      name:University Hospital of Udine
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         name:Department of Oncology, University Hospital of Udine, Udine, Italy
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      name:University Hospital of Udine
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         name:Department of Oncology, University Hospital of Udine, Udine, Italy
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         name:Department of Oncology, University Hospital of Udine, Udine, Italy
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      name:University Hospital of Udine
      address:
         name:Department of Oncology, University Hospital of Udine, Udine, Italy
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      name:University Hospital of Udine
      address:
         name:Department of Oncology, University Hospital of Udine, Udine, Italy
         type:PostalAddress
      name:University Hospital of Udine
      address:
         name:Department of Oncology, University Hospital of Udine, Udine, Italy
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            address:
               name:Department of Oncology, University Hospital of Udine, Udine, Italy
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            name:University of Udine
            address:
               name:Department of Medical and Biological Sciences, University of Udine, Udine, Italy
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            type:Organization
      name:V. Fanotto
      affiliation:
            name:University Hospital of Udine
            address:
               name:Department of Oncology, University Hospital of Udine, Udine, Italy
               type:PostalAddress
            type:Organization
      name:M. Bonotto
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            name:University Hospital of Udine
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               name:Department of Oncology, University Hospital of Udine, Udine, Italy
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      affiliation:
            name:University Hospital of Udine
            address:
               name:Department of Oncology, University Hospital of Udine, Udine, Italy
               type:PostalAddress
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      name:A. M. Minisini
      affiliation:
            name:University Hospital of Udine
            address:
               name:Department of Oncology, University Hospital of Udine, Udine, Italy
               type:PostalAddress
            type:Organization
      name:G. Fasola
      affiliation:
            name:University Hospital of Udine
            address:
               name:Department of Oncology, University Hospital of Udine, Udine, Italy
               type:PostalAddress
            type:Organization
      name:F. Puglisi
      affiliation:
            name:University Hospital of Udine
            address:
               name:Department of Oncology, University Hospital of Udine, Udine, Italy
               type:PostalAddress
            type:Organization
            name:University of Udine
            address:
               name:Department of Medical and Biological Sciences, University of Udine, Udine, Italy
               type:PostalAddress
            type:Organization
      email:[email protected]
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      name:Department of Oncology, University Hospital of Udine, Udine, Italy
      name:Department of Medical and Biological Sciences, University of Udine, Udine, Italy
      name:Department of Oncology, University Hospital of Udine, Udine, Italy
      name:Department of Oncology, University Hospital of Udine, Udine, Italy
      name:Department of Oncology, University Hospital of Udine, Udine, Italy
      name:Department of Oncology, University Hospital of Udine, Udine, Italy
      name:Department of Oncology, University Hospital of Udine, Udine, Italy
      name:Department of Oncology, University Hospital of Udine, Udine, Italy
      name:Department of Medical and Biological Sciences, University of Udine, Udine, Italy
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