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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. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries

We are analyzing https://link.springer.com/article/10.1007/s10555-014-9542-0.

Title:
Immunotherapy of melanoma: Present options and future promises | Cancer and Metastasis Reviews
Description:
Metastatic melanoma is notorious for its immune evasion and resistance to conventional chemotherapy. The recent success of ipilimumab, a human monoclonal antibody against cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4), in increasing the median survival time and stabilizing the disease progression renewed, hopes in treatment for melanoma. Currently, ipilimumab and high-dose interleukin-2 (IL-2; Aldesleukin) are approved as monotherapies for the treatment of patients with unresectable advanced melanoma, and pegylated interferon-α2b (p-IFN-α2b) is approved as an adjuvant for the treatment of patients with surgically resected high-risk melanoma. The present review describes the currently approved immune-modulators and the promising immune-based interventions that are currently in clinical trials. We present the four commonly used strategies to boost immune responses against the tumors; monoclonal antibodies, cytokines, cancer vaccines, and adoptive T cell transfer. The corresponding lists of ongoing clinical trials include details of the trial phase, target patients, intervention details, status of the study, and expected date of completion. Further, our review discusses the challenges faced by immunotherapy and the various strategies adopted to overcome them.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Health & Fitness
  • 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.
However, some sources were not loaded, we suggest to reload the page to get complete results.

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

We can't tell how the site generates income.

Some websites aren't about earning revenue; they're built to connect communities or raise awareness. There are numerous motivations behind creating websites. This might be one of them. Link.springer.com could be getting rich in stealth mode, or the way it's monetizing isn't detectable.

Keywords {🔍}

pubmed, google, scholar, article, cas, melanoma, cancer, journal, clinical, immunotherapy, central, research, human, treatment, patients, therapy, ipilimumab, cell, oncology, advanced, medicine, doi, immunology, cells, metastatic, reviews, review, nature, immune, antibody, ctla, dois, tumor, doiccr, dendritic, privacy, cookies, content, present, rotte, zhou, monoclonal, survival, adjuvant, adoptive, trial, phase, access, gene, activation,

Topics {✒️}

granulocyte-macrophage colony-stimulating factor anti-programmed-death-receptor-1 treatment month download article/chapter b7-related molecule b7-h1 randomised dose-comparison cohort anti-ctla-4 antibody ipilimumab pegylated interferon alpha-2b human t-cell activation inhibitory b7-family molecules van der bruggen promising immune-based interventions immune based therapies immune-related adverse events pd1/pd-l1 axis full article pdf t-cell responses interferon alfa-2b human monoclonal antibody ipilimumab-refractory advanced melanoma high-dose interleukin-2 pegylated interferon-α2b privacy choices/manage cookies peginterferon-alfa-2b adoptive cell therapy targeting mapk pathway tumor-infiltrating cd8+ current gene therapy cancer consensus statement dermatologic adverse events cd27/cd70 pathway b7 family revisited main stumbling blocks severe adverse events localized stage progression ifn-gamma production targeting human cd27 adoptive cell immunotherapy van den eynde xenogeneic human tyrosinase cytotoxic t-lymphocyte biological rationale dermatological treatment human gene mage-1 durable tumor remission tumor-infiltrating lymphocytes costimulatory b7-h1 human vaccin immunotherapy nature reviews cancer drug administration approval cd27-expressing lymphoma

Questions {❓}

  • Psychological care for people with melanoma: what, when, why and how?
  • Psychological stress and melanoma: are we meeting our patients’ psychological needs?

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Immunotherapy of melanoma: Present options and future promises
         description:Metastatic melanoma is notorious for its immune evasion and resistance to conventional chemotherapy. The recent success of ipilimumab, a human monoclonal antibody against cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4), in increasing the median survival time and stabilizing the disease progression renewed, hopes in treatment for melanoma. Currently, ipilimumab and high-dose interleukin-2 (IL-2; Aldesleukin) are approved as monotherapies for the treatment of patients with unresectable advanced melanoma, and pegylated interferon-α2b (p-IFN-α2b) is approved as an adjuvant for the treatment of patients with surgically resected high-risk melanoma. The present review describes the currently approved immune-modulators and the promising immune-based interventions that are currently in clinical trials. We present the four commonly used strategies to boost immune responses against the tumors; monoclonal antibodies, cytokines, cancer vaccines, and adoptive T cell transfer. The corresponding lists of ongoing clinical trials include details of the trial phase, target patients, intervention details, status of the study, and expected date of completion. Further, our review discusses the challenges faced by immunotherapy and the various strategies adopted to overcome them.
         datePublished:2015-01-15T00:00:00Z
         dateModified:2015-01-15T00:00:00Z
         pageStart:115
         pageEnd:128
         sameAs:https://doi.org/10.1007/s10555-014-9542-0
         keywords:
            Melanoma
            Immunotherapy
            Ipilimumab
            Vaccines
            Clinical trials
            Cancer Research
            Oncology
            Biomedicine
            general
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               name:Youwen Zhou
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                     name:University of British Columbia
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                        name:Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
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      headline:Immunotherapy of melanoma: Present options and future promises
      description:Metastatic melanoma is notorious for its immune evasion and resistance to conventional chemotherapy. The recent success of ipilimumab, a human monoclonal antibody against cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4), in increasing the median survival time and stabilizing the disease progression renewed, hopes in treatment for melanoma. Currently, ipilimumab and high-dose interleukin-2 (IL-2; Aldesleukin) are approved as monotherapies for the treatment of patients with unresectable advanced melanoma, and pegylated interferon-α2b (p-IFN-α2b) is approved as an adjuvant for the treatment of patients with surgically resected high-risk melanoma. The present review describes the currently approved immune-modulators and the promising immune-based interventions that are currently in clinical trials. We present the four commonly used strategies to boost immune responses against the tumors; monoclonal antibodies, cytokines, cancer vaccines, and adoptive T cell transfer. The corresponding lists of ongoing clinical trials include details of the trial phase, target patients, intervention details, status of the study, and expected date of completion. Further, our review discusses the challenges faced by immunotherapy and the various strategies adopted to overcome them.
      datePublished:2015-01-15T00:00:00Z
      dateModified:2015-01-15T00:00:00Z
      pageStart:115
      pageEnd:128
      sameAs:https://doi.org/10.1007/s10555-014-9542-0
      keywords:
         Melanoma
         Immunotherapy
         Ipilimumab
         Vaccines
         Clinical trials
         Cancer Research
         Oncology
         Biomedicine
         general
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            name:Anand Rotte
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                  name:University of British Columbia
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                     name:Vancouver Coastal Health Research Institute, Vancouver, Canada
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            name:Madhuri Bhandaru
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                  name:University of British Columbia
                  address:
                     name:Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
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                  address:
                     name:Vancouver Coastal Health Research Institute, Vancouver, Canada
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            name:Youwen Zhou
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                     name:Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
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                     name:Vancouver Coastal Health Research Institute, Vancouver, Canada
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                     name:Dermatologic Oncology Program, British Columbia Cancer Agency, Vancouver, Canada
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                  type:Organization
            type:Person
            name:Kevin J. McElwee
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                  name:University of British Columbia
                  address:
                     name:Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
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         name:Vancouver Coastal Health Research Institute, Vancouver, Canada
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         name:Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
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         name:Vancouver Coastal Health Research Institute, Vancouver, Canada
         type:PostalAddress
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      address:
         name:Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
         type:PostalAddress
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      address:
         name:Vancouver Coastal Health Research Institute, Vancouver, Canada
         type:PostalAddress
      name:British Columbia Cancer Agency
      address:
         name:Dermatologic Oncology Program, British Columbia Cancer Agency, Vancouver, Canada
         type:PostalAddress
      name:University of British Columbia
      address:
         name:Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
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               type:PostalAddress
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            name:Vancouver Coastal Health Research Institute
            address:
               name:Vancouver Coastal Health Research Institute, Vancouver, Canada
               type:PostalAddress
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      email:[email protected]
      name:Madhuri Bhandaru
      affiliation:
            name:University of British Columbia
            address:
               name:Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
               type:PostalAddress
            type:Organization
            name:Vancouver Coastal Health Research Institute
            address:
               name:Vancouver Coastal Health Research Institute, Vancouver, Canada
               type:PostalAddress
            type:Organization
      name:Youwen Zhou
      affiliation:
            name:University of British Columbia
            address:
               name:Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
               type:PostalAddress
            type:Organization
            name:Vancouver Coastal Health Research Institute
            address:
               name:Vancouver Coastal Health Research Institute, Vancouver, Canada
               type:PostalAddress
            type:Organization
            name:British Columbia Cancer Agency
            address:
               name:Dermatologic Oncology Program, British Columbia Cancer Agency, Vancouver, Canada
               type:PostalAddress
            type:Organization
      name:Kevin J. McElwee
      affiliation:
            name:University of British Columbia
            address:
               name:Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
               type:PostalAddress
            type:Organization
            name:Vancouver Coastal Health Research Institute
            address:
               name:Vancouver Coastal Health Research Institute, Vancouver, Canada
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            type:Organization
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      name:Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
      name:Vancouver Coastal Health Research Institute, Vancouver, Canada
      name:Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
      name:Vancouver Coastal Health Research Institute, Vancouver, Canada
      name:Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
      name:Vancouver Coastal Health Research Institute, Vancouver, Canada
      name:Dermatologic Oncology Program, British Columbia Cancer Agency, Vancouver, Canada
      name:Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
      name:Vancouver Coastal Health Research Institute, Vancouver, Canada
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External Links {🔗}(347)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

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