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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
  8. Schema
  9. External Links
  10. Analytics And Tracking
  11. Libraries
  12. CDN Services

We are analyzing https://link.springer.com/article/10.1007/s10549-004-2756-z.

Title:
Impact of metastatic estrogen receptor and progesterone receptor status on survival | Breast Cancer Research and Treatment
Description:
Hormone responsive breast cancer is usually determined by the presence of estrogen receptors (ER) or progesterone receptors (PR) on primary invasive breast cancers. Adjuvant and metastatic hormone therapy are recommended based on primary ER and PR determination. Little information is available to determine if primary hormone receptors correlate with metastatic disease and if survival is influenced by metastatic receptor status. We retrospectively compared primary to metastatic tumor ER and PR content from 200 metastatic breast cancer patients. ER and PR analyses were available in both primary and metastatic disease in 200 and 173 patients, respectively. There was a correlation between both the ER and PR in the primary and metastatic lesion (p < 0.001). However, in 60 of 200 (30%) patients, discordance between primary and metastatic ER was noted. Tumors from 68 of 173 (39.3%) showed discordance for PR. In 39 (19.5%) patients, the ER primary status was positive and metastatic status was negative and in 21 (10.5%) patients, the primary status was negative and metastatic status was positive. Survival from the time of metastatic diagnosis was calculated. Those patients with ER positive primary and metastatic tumors (Positive/Positive) or only the metastatic lesion (Negative/Positive) had similar median survival (1131 and 1111 days, respectively). However, patients with tumors that changed from positive primary to negative metastasis (Positive/Negative) experienced significantly shorter median survival (669 days, p < 0.05). Likewise, median survival (580 days) was significantly shorter for patients with primary and metastasis ER negative (Negative/Negative, p < 0.001) compared to Positive/Positive (p < 0.001) or compared to Negative/Positive (p < 0.02). The changes in PR status were not associated with a change in survival. We found a significant discordance between hormone receptor content of primary versus metastatic breast cancer. The ER status of the metastatic lesion was a better predictor of survival. Therefore, optimal metastatic treatment cannot be determined solely on primary ER and PR analysis.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Health & Fitness
  • Science
  • Politics

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 8,149,968 visitors per month in the current month.

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

The income method remains a mystery to us.

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 be making money, but it's not detectable how they're doing it.

Keywords {🔍}

cancer, breast, google, scholar, primary, receptor, metastatic, estrogen, status, survival, article, progesterone, receptors, res, hormone, therapy, content, lower, patients, oncol, discordance, access, human, endocrine, clin, treat, privacy, cookies, analysis, research, treatment, elyse, cincinnati, information, publish, search, cancers, positive, negative, recurrent, osborne, advanced, eur, data, log, journal, glass, bradley, blau, compared,

Topics {✒️}

berardo gm clark morrow ck osborne human breast cancer early breast cancer advanced breast cancer metastatic breast cancer recurrent breast cancer month download article/chapter primary breast cancer recurrent breast cancers phase iii study secondary breast carcinomas primary breast carcinomas asynchronous metastatic/recurrent sites breast cancer metastatic hormone therapy hormone receptor content hormone receptor status p53 mutation int full article pdf receptor expression discordance privacy choices/manage cookies metastatic estrogen receptor multiple intratumoral assays metastatic receptor status progesterone receptor eur buzdar jf robertson article lower progesterone receptor activity progesterone receptor concordance letrozole versus tamoxifen oestrogen receptor concentration estrogen receptor variants estrogen receptor mutations metastatic tumor er check access instant access optimal metastatic treatment progesterone receptor status european economic area related subjects gazder dl stahl hollander da wolfe goldhirsch wh hartmann molteni rb duda kamby bb rasmussen heterogeneous gene alterations her2 gene amplification oestrogen receptor status conditions privacy policy

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Impact of metastatic estrogen receptor and progesterone receptor status on survival
         description:Hormone responsive breast cancer is usually determined by the presence of estrogen receptors (ER) or progesterone receptors (PR) on primary invasive breast cancers. Adjuvant and metastatic hormone therapy are recommended based on primary ER and PR determination. Little information is available to determine if primary hormone receptors correlate with metastatic disease and if survival is influenced by metastatic receptor status. We retrospectively compared primary to metastatic tumor ER and PR content from 200 metastatic breast cancer patients. ER and PR analyses were available in both primary and metastatic disease in 200 and 173 patients, respectively. There was a correlation between both the ER and PR in the primary and metastatic lesion (p < 0.001). However, in 60 of 200 (30%) patients, discordance between primary and metastatic ER was noted. Tumors from 68 of 173 (39.3%) showed discordance for PR. In 39 (19.5%) patients, the ER primary status was positive and metastatic status was negative and in 21 (10.5%) patients, the primary status was negative and metastatic status was positive. Survival from the time of metastatic diagnosis was calculated. Those patients with ER positive primary and metastatic tumors (Positive/Positive) or only the metastatic lesion (Negative/Positive) had similar median survival (1131 and 1111 days, respectively). However, patients with tumors that changed from positive primary to negative metastasis (Positive/Negative) experienced significantly shorter median survival (669 days, p < 0.05). Likewise, median survival (580 days) was significantly shorter for patients with primary and metastasis ER negative (Negative/Negative, p < 0.001) compared to Positive/Positive (p < 0.001) or compared to Negative/Positive (p < 0.02). The changes in PR status were not associated with a change in survival. We found a significant discordance between hormone receptor content of primary versus metastatic breast cancer. The ER status of the metastatic lesion was a better predictor of survival. Therefore, optimal metastatic treatment cannot be determined solely on primary ER and PR analysis.
         datePublished:
         dateModified:
         pageStart:65
         pageEnd:70
         sameAs:https://doi.org/10.1007/s10549-004-2756-z
         keywords:
            Breast cancer
            estrogen receptors
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            metastatic hormone receptors
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         image:
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      headline:Impact of metastatic estrogen receptor and progesterone receptor status on survival
      description:Hormone responsive breast cancer is usually determined by the presence of estrogen receptors (ER) or progesterone receptors (PR) on primary invasive breast cancers. Adjuvant and metastatic hormone therapy are recommended based on primary ER and PR determination. Little information is available to determine if primary hormone receptors correlate with metastatic disease and if survival is influenced by metastatic receptor status. We retrospectively compared primary to metastatic tumor ER and PR content from 200 metastatic breast cancer patients. ER and PR analyses were available in both primary and metastatic disease in 200 and 173 patients, respectively. There was a correlation between both the ER and PR in the primary and metastatic lesion (p < 0.001). However, in 60 of 200 (30%) patients, discordance between primary and metastatic ER was noted. Tumors from 68 of 173 (39.3%) showed discordance for PR. In 39 (19.5%) patients, the ER primary status was positive and metastatic status was negative and in 21 (10.5%) patients, the primary status was negative and metastatic status was positive. Survival from the time of metastatic diagnosis was calculated. Those patients with ER positive primary and metastatic tumors (Positive/Positive) or only the metastatic lesion (Negative/Positive) had similar median survival (1131 and 1111 days, respectively). However, patients with tumors that changed from positive primary to negative metastasis (Positive/Negative) experienced significantly shorter median survival (669 days, p < 0.05). Likewise, median survival (580 days) was significantly shorter for patients with primary and metastasis ER negative (Negative/Negative, p < 0.001) compared to Positive/Positive (p < 0.001) or compared to Negative/Positive (p < 0.02). The changes in PR status were not associated with a change in survival. We found a significant discordance between hormone receptor content of primary versus metastatic breast cancer. The ER status of the metastatic lesion was a better predictor of survival. Therefore, optimal metastatic treatment cannot be determined solely on primary ER and PR analysis.
      datePublished:
      dateModified:
      pageStart:65
      pageEnd:70
      sameAs:https://doi.org/10.1007/s10549-004-2756-z
      keywords:
         Breast cancer
         estrogen receptors
         hormone therapy
         metastatic hormone receptors
         Oncology
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      isPartOf:
         name:Breast Cancer Research and Treatment
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                     name:Oncology–Hematology Care, Cincinnati, USA
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                     name:Oncology–Hematology Care, Cincinnati, USA
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         name:Department of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati
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         name:Oncology–Hematology Care, Cincinnati, USA
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               type:PostalAddress
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            name:Oncology–Hematology Care
            address:
               name:Oncology–Hematology Care, Cincinnati, USA
               type:PostalAddress
            type:Organization
            name:University of Cincinnati Medical Center
            address:
               name:University of Cincinnati Medical Center, Cincinnati, USA
               type:PostalAddress
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      affiliation:
            name:University of Cincinnati College of Medicine
            address:
               name:Department of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati
               type:PostalAddress
            type:Organization
      name:Robbin Blau
      affiliation:
            name:Oncology–Hematology Care
            address:
               name:Oncology–Hematology Care, Cincinnati, USA
               type:PostalAddress
            type:Organization
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      affiliation:
            name:Oncology–Hematology Care
            address:
               name:Oncology–Hematology Care, Cincinnati, USA
               type:PostalAddress
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      name:Department of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati
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      name:Department of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati
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      name:Oncology–Hematology Care, Cincinnati, USA
      name:Oncology–Hematology Care, Cincinnati, USA
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External Links {🔗}(69)

Analytics and Tracking {📊}

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Libraries {📚}

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CDN Services {📦}

  • Crossref

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