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We are analyzing https://link.springer.com/article/10.1186/s40425-018-0323-0.

Title:
Granulomatous/sarcoid-like lesions associated with checkpoint inhibitors: a marker of therapy response in a subset of melanoma patients | Journal for ImmunoTherapy of Cancer
Description:
Background Immune checkpoint therapy has dramatically changed the landscape of cancer therapy, providing an efficacious and durable therapeutic option for patients with advanced-stage disease. However, dermatologic toxicities are a well-recognized side effect in patients receiving this therapy. A spectrum of immune related adverse events (irAEs) involving the skin can occur and include immunobullous disorders, lichenoid dermatitis, and vitiligo. Granulomatous/sarcoid-like lesions are now being recognized with the current class of checkpoint inhibitors (CPIs) that involve the dermis, the subcutaneous tissue (panniculitis), and lymph nodes. Case presentation We report 3 patients who developed granulomatous/sarcoid-like lesions while being treated with immune checkpoint therapy for advanced-stage melanoma, and we provide a comprehensive review of the literature in which similar cases are described. To date, 26 patients (including the 3 from this report) have been described with a median age of 57 years who developed granulomatous/sarcoid-like lesions associated with CPIs (median onset 6 months), of which 77% of patients had melanoma as primary tumor. To manage this adverse side effect, therapy was withheld in 38% of patients and 44% of the patients were treated with systemic steroids and 8% patients with localized therapy (one patient with intralesional triamcinolone). 96% of patients demonstrated either resolution or improvement of granulomatous/sarcoid-like lesions associated with CPIs irrespective of medical intervention. Therapeutic response, stable disease, or remission of primary malignancy was observed in 71% of reported patients who developed granulomatous/sarcoid-like lesions associated with CPIs over a median follow-up of 11.5 months since initiation of treatment. Conclusions The development of granulomatous/sarcoid-like lesions associated with CPIs is a recognized manifestation with the current class of immune checkpoint therapy that may clinically and radiographically mimic disease recurrence. Awareness of this type of toxicity is important for appropriate management and possible measurement of therapeutic response in a subset of patients who manifest this type of immune-mediated reaction.
Website Age:
28 years and 1 months (reg. 1997-05-29).

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  • Health & Fitness
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What CMS is link.springer.com built with?

Custom-built

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


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Keywords {🔍}

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Topics {✒️}

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Questions {❓}

  • Exacerbation of recalcitrant cutaneous sarcoidosis with adalimumab--a paradoxical effect?
  • Immunopathogenesis of sarcoidosis and risk of malignancy: a lost truth?
  • Sarcoidosis-like lesions: another paradoxical reaction to anti-TNF therapy?

Schema {🗺️}

WebPage:
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         headline:Granulomatous/sarcoid-like lesions associated with checkpoint inhibitors: a marker of therapy response in a subset of melanoma patients
         description:Immune checkpoint therapy has dramatically changed the landscape of cancer therapy, providing an efficacious and durable therapeutic option for patients with advanced-stage disease. However, dermatologic toxicities are a well-recognized side effect in patients receiving this therapy. A spectrum of immune related adverse events (irAEs) involving the skin can occur and include immunobullous disorders, lichenoid dermatitis, and vitiligo. Granulomatous/sarcoid-like lesions are now being recognized with the current class of checkpoint inhibitors (CPIs) that involve the dermis, the subcutaneous tissue (panniculitis), and lymph nodes. We report 3 patients who developed granulomatous/sarcoid-like lesions while being treated with immune checkpoint therapy for advanced-stage melanoma, and we provide a comprehensive review of the literature in which similar cases are described. To date, 26 patients (including the 3 from this report) have been described with a median age of 57 years who developed granulomatous/sarcoid-like lesions associated with CPIs (median onset 6 months), of which 77% of patients had melanoma as primary tumor. To manage this adverse side effect, therapy was withheld in 38% of patients and 44% of the patients were treated with systemic steroids and 8% patients with localized therapy (one patient with intralesional triamcinolone). 96% of patients demonstrated either resolution or improvement of granulomatous/sarcoid-like lesions associated with CPIs irrespective of medical intervention. Therapeutic response, stable disease, or remission of primary malignancy was observed in 71% of reported patients who developed granulomatous/sarcoid-like lesions associated with CPIs over a median follow-up of 11.5 months since initiation of treatment. The development of granulomatous/sarcoid-like lesions associated with CPIs is a recognized manifestation with the current class of immune checkpoint therapy that may clinically and radiographically mimic disease recurrence. Awareness of this type of toxicity is important for appropriate management and possible measurement of therapeutic response in a subset of patients who manifest this type of immune-mediated reaction.
         datePublished:2018-02-12T00:00:00Z
         dateModified:2018-02-12T00:00:00Z
         pageStart:1
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         keywords:
            Checkpoint Inhibitors (CPIs)
            Immune Checkpoint Therapy
            Dermatologic Toxicity
            Pembrolizumab Therapy
            Positron Emission tomography-CT (PET/CT)
            Oncology
            Immunology
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      headline:Granulomatous/sarcoid-like lesions associated with checkpoint inhibitors: a marker of therapy response in a subset of melanoma patients
      description:Immune checkpoint therapy has dramatically changed the landscape of cancer therapy, providing an efficacious and durable therapeutic option for patients with advanced-stage disease. However, dermatologic toxicities are a well-recognized side effect in patients receiving this therapy. A spectrum of immune related adverse events (irAEs) involving the skin can occur and include immunobullous disorders, lichenoid dermatitis, and vitiligo. Granulomatous/sarcoid-like lesions are now being recognized with the current class of checkpoint inhibitors (CPIs) that involve the dermis, the subcutaneous tissue (panniculitis), and lymph nodes. We report 3 patients who developed granulomatous/sarcoid-like lesions while being treated with immune checkpoint therapy for advanced-stage melanoma, and we provide a comprehensive review of the literature in which similar cases are described. To date, 26 patients (including the 3 from this report) have been described with a median age of 57 years who developed granulomatous/sarcoid-like lesions associated with CPIs (median onset 6 months), of which 77% of patients had melanoma as primary tumor. To manage this adverse side effect, therapy was withheld in 38% of patients and 44% of the patients were treated with systemic steroids and 8% patients with localized therapy (one patient with intralesional triamcinolone). 96% of patients demonstrated either resolution or improvement of granulomatous/sarcoid-like lesions associated with CPIs irrespective of medical intervention. Therapeutic response, stable disease, or remission of primary malignancy was observed in 71% of reported patients who developed granulomatous/sarcoid-like lesions associated with CPIs over a median follow-up of 11.5 months since initiation of treatment. The development of granulomatous/sarcoid-like lesions associated with CPIs is a recognized manifestation with the current class of immune checkpoint therapy that may clinically and radiographically mimic disease recurrence. Awareness of this type of toxicity is important for appropriate management and possible measurement of therapeutic response in a subset of patients who manifest this type of immune-mediated reaction.
      datePublished:2018-02-12T00:00:00Z
      dateModified:2018-02-12T00:00:00Z
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      keywords:
         Checkpoint Inhibitors (CPIs)
         Immune Checkpoint Therapy
         Dermatologic Toxicity
         Pembrolizumab Therapy
         Positron Emission tomography-CT (PET/CT)
         Oncology
         Immunology
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         name:BioMed Central
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                     type:PostalAddress
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                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Translational and Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
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            name:Kelly C. Nelson
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                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Dermatology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Adi Diab
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Gregg A. Staerkel
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Pathology, Section of Cytopathology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Priyadharsini Nagarajan
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Pathology, Section of Dermatopathology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
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            name:Carlos A. Torres-Cabala
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Pathology, Section of Dermatopathology, The University of Texas MD Anderson Cancer Center, Houston, USA
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                  name:The University of Texas MD Anderson Cancer Center
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                     name:Department of Dermatology, The University of Texas MD Anderson Cancer Center, Houston, USA
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            name:Beth A. Chasen
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Nuclear Medicine, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Jennifer A. Wargo
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Victor G. Prieto
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Pathology, Section of Dermatopathology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Dermatology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Rodabe N. Amaria
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Jonathan L. Curry
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Pathology, Section of Dermatopathology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
                  name:The University of Texas MD Anderson Cancer Center
                  address:
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      issn:
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         name:Department of Pathology, Section of Dermatopathology, The University of Texas MD Anderson Cancer Center, Houston, USA
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      address:
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      address:
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         name:Department of Dermatology, The University of Texas MD Anderson Cancer Center, Houston, USA
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      name:Kelly C. Nelson
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            name:The University of Texas MD Anderson Cancer Center
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               type:PostalAddress
            type:Organization
      name:Adi Diab
      affiliation:
            name:The University of Texas MD Anderson Cancer Center
            address:
               name:Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
               type:PostalAddress
            type:Organization
      name:Gregg A. Staerkel
      affiliation:
            name:The University of Texas MD Anderson Cancer Center
            address:
               name:Department of Pathology, Section of Cytopathology, The University of Texas MD Anderson Cancer Center, Houston, USA
               type:PostalAddress
            type:Organization
      name:Priyadharsini Nagarajan
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            name:The University of Texas MD Anderson Cancer Center
            address:
               name:Department of Pathology, Section of Dermatopathology, The University of Texas MD Anderson Cancer Center, Houston, USA
               type:PostalAddress
            type:Organization
      name:Carlos A. Torres-Cabala
      affiliation:
            name:The University of Texas MD Anderson Cancer Center
            address:
               name:Department of Pathology, Section of Dermatopathology, The University of Texas MD Anderson Cancer Center, Houston, USA
               type:PostalAddress
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            name:The University of Texas MD Anderson Cancer Center
            address:
               name:Department of Dermatology, The University of Texas MD Anderson Cancer Center, Houston, USA
               type:PostalAddress
            type:Organization
      name:Beth A. Chasen
      affiliation:
            name:The University of Texas MD Anderson Cancer Center
            address:
               name:Department of Nuclear Medicine, The University of Texas MD Anderson Cancer Center, Houston, USA
               type:PostalAddress
            type:Organization
      name:Jennifer A. Wargo
      affiliation:
            name:The University of Texas MD Anderson Cancer Center
            address:
               name:Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
               type:PostalAddress
            type:Organization
      name:Victor G. Prieto
      affiliation:
            name:The University of Texas MD Anderson Cancer Center
            address:
               name:Department of Pathology, Section of Dermatopathology, The University of Texas MD Anderson Cancer Center, Houston, USA
               type:PostalAddress
            type:Organization
            name:The University of Texas MD Anderson Cancer Center
            address:
               name:Department of Dermatology, The University of Texas MD Anderson Cancer Center, Houston, USA
               type:PostalAddress
            type:Organization
      name:Rodabe N. Amaria
      affiliation:
            name:The University of Texas MD Anderson Cancer Center
            address:
               name:Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
               type:PostalAddress
            type:Organization
      name:Jonathan L. Curry
      affiliation:
            name:The University of Texas MD Anderson Cancer Center
            address:
               name:Department of Pathology, Section of Dermatopathology, The University of Texas MD Anderson Cancer Center, Houston, USA
               type:PostalAddress
            type:Organization
            name:The University of Texas MD Anderson Cancer Center
            address:
               name:Department of Dermatology, The University of Texas MD Anderson Cancer Center, Houston, USA
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Department of Pathology, Section of Dermatopathology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Translational and Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Dermatology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Pathology, Section of Cytopathology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Pathology, Section of Dermatopathology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Pathology, Section of Dermatopathology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Dermatology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Nuclear Medicine, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Pathology, Section of Dermatopathology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Dermatology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Pathology, Section of Dermatopathology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Dermatology, The University of Texas MD Anderson Cancer Center, Houston, USA

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