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LINK . SPRINGER . COM {}

  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
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We are analyzing https://link.springer.com/article/10.1007/s10549-007-9645-1.

Title:
Epidermal growth factor receptor (EGFR) and the estrogen receptor modulator amplified in breast cancer (AIB1) for predicting clinical outcome after adjuvant tamoxifen in breast cancer | Breast Cancer Research and Treatment
Description:
The epidermal growth factor receptor (EGFR) and the estrogen receptor (ER) modulator Amplified In Breast cancer-1 (AIB1) have been reported to be of importance for the prognosis of breast cancer patients. We have analyzed AIB1 and EGFR by immunohistochemistry in primary breast cancers (n = 297) arranged in a tissue microarray in order to predict outcome after adjuvant endocrine therapy with tamoxifen for two years. High expression of AIB1 was associated with DNA-nondiploidy, high S-phase fraction, HER2 amplification, and short term (≀2 years) distant disease-free survival (DDFS), independent of ER status. High expression of EGFR was strongly associated to ER negativity and also correlated with progesterone receptor negativity, high S-phase fraction, and inversely correlated with nodal metastases. In univariate analysis, high EGFR was associated with shorter DDFS (hazard ratio 2.1; P = 0.017), and reached borderline significance in a multivariate analysis, adjusting for ER, menopausal and lymph node status, tumor size, and HER2 (P = 0.057). In conclusion, both AIB1 and EGFR were associated to DDFS for breast cancer patients treated with two years of adjuvant tamoxifen; AIB1 with the development of early distant recurrences, indicating association between high AIB1 and resistance to tamoxifen during treatment, and EGFR with distant recurrences up to a follow up of five years.
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 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💾}

We see no obvious way the site makes money.

Not all websites are made for profit; some exist to inform or educate users. Or any other reason why people make websites. And this might be the case. Link.springer.com might have a hidden revenue stream, but it's not something we can detect.

Keywords {🔍}

cancer, breast, article, google, scholar, receptor, cas, pubmed, tamoxifen, growth, factor, estrogen, aib, egfr, adjuvant, clin, epidermal, patients, res, therapy, expression, research, clinical, endocrine, resistance, lund, years, high, early, access, oncol, privacy, cookies, content, fernö, trial, receptorpositive, suppl, osborne, university, data, publish, search, treatment, amplified, predicting, bendahl, prognosis, primary, distant,

Topics {✒}

primary breast cancers month download article/chapter node-negative breast caner steroid hormone receptors hormone receptor-positive growth factor pathways early breast cancer high s-phase fraction distant disease-free survival human breast cancer swedish research council postmenopausal breast cancer breast cancer cells swedish cancer society early distant recurrences breast cancer patients estrogen receptor–positive full article pdf breast cancer samples privacy choices/manage cookies erbb-2 signaling activity estrogen receptor status progesterone receptor negativity lund research foundation lymph node status potentially predictive markers elisabeth nilsson foundation adjuvant s-1 therapy european economic area semi-quantitative scoring overcoming endocrine resistance breast cancer breast cancer-1 breast cancer 1 conditions privacy policy article dihge twenty-year results endocrine therapy resistance steroid receptors reached borderline significance predicting clinical outcome pĂ€r-ola bendahl check access instant access accepting optional cookies adjuvant endocrine therapy tamoxifen response adjuvant tamoxifen therapy year median follow mĂ„rten fernö

Schema {đŸ—ș}

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         headline:Epidermal growth factor receptor (EGFR) and the estrogen receptor modulator amplified in breast cancer (AIB1) for predicting clinical outcome after adjuvant tamoxifen in breast cancer
         description:The epidermal growth factor receptor (EGFR) and the estrogen receptor (ER) modulator Amplified In Breast cancer-1 (AIB1) have been reported to be of importance for the prognosis of breast cancer patients. We have analyzed AIB1 and EGFR by immunohistochemistry in primary breast cancers (n = 297) arranged in a tissue microarray in order to predict outcome after adjuvant endocrine therapy with tamoxifen for two years. High expression of AIB1 was associated with DNA-nondiploidy, high S-phase fraction, HER2 amplification, and short term (≀2 years) distant disease-free survival (DDFS), independent of ER status. High expression of EGFR was strongly associated to ER negativity and also correlated with progesterone receptor negativity, high S-phase fraction, and inversely correlated with nodal metastases. In univariate analysis, high EGFR was associated with shorter DDFS (hazard ratio 2.1; P = 0.017), and reached borderline significance in a multivariate analysis, adjusting for ER, menopausal and lymph node status, tumor size, and HER2 (P = 0.057). In conclusion, both AIB1 and EGFR were associated to DDFS for breast cancer patients treated with two years of adjuvant tamoxifen; AIB1 with the development of early distant recurrences, indicating association between high AIB1 and resistance to tamoxifen during treatment, and EGFR with distant recurrences up to a follow up of five years.
         datePublished:2007-07-17T00:00:00Z
         dateModified:2007-07-17T00:00:00Z
         pageStart:255
         pageEnd:262
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            Prognosis
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            Tamoxifen
            Oncology
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      headline:Epidermal growth factor receptor (EGFR) and the estrogen receptor modulator amplified in breast cancer (AIB1) for predicting clinical outcome after adjuvant tamoxifen in breast cancer
      description:The epidermal growth factor receptor (EGFR) and the estrogen receptor (ER) modulator Amplified In Breast cancer-1 (AIB1) have been reported to be of importance for the prognosis of breast cancer patients. We have analyzed AIB1 and EGFR by immunohistochemistry in primary breast cancers (n = 297) arranged in a tissue microarray in order to predict outcome after adjuvant endocrine therapy with tamoxifen for two years. High expression of AIB1 was associated with DNA-nondiploidy, high S-phase fraction, HER2 amplification, and short term (≀2 years) distant disease-free survival (DDFS), independent of ER status. High expression of EGFR was strongly associated to ER negativity and also correlated with progesterone receptor negativity, high S-phase fraction, and inversely correlated with nodal metastases. In univariate analysis, high EGFR was associated with shorter DDFS (hazard ratio 2.1; P = 0.017), and reached borderline significance in a multivariate analysis, adjusting for ER, menopausal and lymph node status, tumor size, and HER2 (P = 0.057). In conclusion, both AIB1 and EGFR were associated to DDFS for breast cancer patients treated with two years of adjuvant tamoxifen; AIB1 with the development of early distant recurrences, indicating association between high AIB1 and resistance to tamoxifen during treatment, and EGFR with distant recurrences up to a follow up of five years.
      datePublished:2007-07-17T00:00:00Z
      dateModified:2007-07-17T00:00:00Z
      pageStart:255
      pageEnd:262
      sameAs:https://doi.org/10.1007/s10549-007-9645-1
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         AIB1
         Breast cancer
         EGFR
         Prognosis
         Resistance
         Tamoxifen
         Oncology
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         name:Department of Surgery, Clinical Sciences, University of Lund, Lund, Sweden
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               type:PostalAddress
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            address:
               name:Department of Pathology, Clinical Sciences, University of Lund, Lund, Sweden
               type:PostalAddress
            type:Organization
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      affiliation:
            name:University of Tampere
            address:
               name:Institute of Medical Technology, University of Tampere, Tampere, Finland
               type:PostalAddress
            type:Organization
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      affiliation:
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            address:
               name:Department of Oncology, Clinical Sciences, University of Lund, Lund, Sweden
               type:PostalAddress
            type:Organization
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               name:Department of Surgery, Clinical Sciences, University of Lund, Lund, Sweden
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            name:University of Lund
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      name:Institute of Medical Technology, University of Tampere, Tampere, Finland
      name:Department of Oncology, Clinical Sciences, University of Lund, Lund, Sweden
      name:Department of Surgery, Clinical Sciences, University of Lund, Lund, Sweden
      name:Department of Oncology, Clinical Sciences, University of Lund, Lund, Sweden
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External Links {🔗}(103)

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