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article, pubmed, cancer, google, scholar, cell, squamous, head, neck, cas, carcinoma, survival, content, central, laryngeal, patients, til, lymphocytes, oncol, university, michigan, analysis, thomas, chad, brenner, tumor, infiltrating, ann, usa, mann, lscc, cells, arbor, tumorinfiltrating, birkeland, wolf, matthew, spector, recurrentpersistent, prognostic, clin, oral, department, privacy, cookies, memory, jacqueline, smith, andrew, bellile,

Topics {✒️}

tissue-resident memory features month download article/chapter tumor-infiltrating lymphocytes expressing small-cell lung cancer nih grants u01-de025184 nih grant f31-de02760001 nih grant t32-dc535615 american joint committee article cancer immunology related subjects tumor-infiltrating lymphocytes tumor infiltrating lymphocytes cd1a-positive dendritic cells tumor-infiltrating lymphocyte full article pdf advanced laryngeal cancer tumor-infiltrating regulatory recurrent/persistent lscc immune profile driven privacy choices/manage cookies advanced larynx cancer human ovarian cancer cd103+ til content long-term results human lung cancer prognostic markers cd103+ til status cd103+ til levels neck cancer identifies salvage laryngectomy specimens medical center dr tumor lymphocytic infiltration neck spore program disease-specific survival disease-free survival infiltrating lymphocytes pd-l1+ european economic area os hazard ratio personalized treatment paradigms nonsurgical treatment strategies biologically distinct hpv cutpoint determination methods copy number alterations jbm ensured quality ethics declarations conflict �immune-rich” phenotype carey received funding smith received funding conditions privacy policy

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WebPage:
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         headline:Analysis of tumor-infiltrating CD103 resident memory T-cell content in recurrent laryngeal squamous cell carcinoma
         description:Recurrent laryngeal squamous cell carcinomas (LSCCs) are associated with poor outcomes, without reliable biomarkers to identify patients who may benefit from adjuvant therapies. Given the emergence of tumor-infiltrating lymphocytes (TIL) as a biomarker in head and neck squamous cell carcinoma, we generated predictive models to understand the utility of CD4+, CD8+ and/or CD103+ TIL status in patients with advanced LSCC. Tissue microarrays were constructed from salvage laryngectomy specimens of 183 patients with recurrent/persistent LSCC and independently stained for CD4+, CD8+, and CD103+ TIL content. Cox proportional hazards regression analysis was employed to assess combinations of CD4+, CD8+, and CD103+ TIL levels for prediction of overall survival (OS), disease-specific survival (DSS), and disease-free survival (DFS) in patients with recurrent/persistent LSCC. High tumor CD103+ TIL content was associated with significantly improved OS, DSS, and DFS and was a stronger predictor of survival in recurrent/persistent LSCC than either high CD8+ or CD4+ TIL content. On multivariate analysis, an “immune-rich” phenotype, in which tumors were enriched for both CD103+ and CD4+ TILs, conferred a survival benefit (OS hazard ratio: 0.28, p = 0.0014; DSS hazard ratio: 0.09, p = 0.0015; DFS hazard ratio: 0.18, p = 0.0018) in recurrent/persistent LSCC. An immune profile driven by CD103+ TIL content, alone and in combination with CD4+ TIL content, is a prognostic biomarker of survival in patients with recurrent/persistent LSCC. Predictive models described herein may thus prove valuable in prognostic stratification and lead to personalized treatment paradigms for this patient population.
         datePublished:2018-10-25T00:00:00Z
         dateModified:2018-10-25T00:00:00Z
         pageStart:213
         pageEnd:220
         sameAs:https://doi.org/10.1007/s00262-018-2256-3
         keywords:
            CD103
            Resident memory
            T-cell
            HNSCC
            Larynx
            Oncology
            Immunology
            Cancer Research
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               name:Emily Bellile
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      headline:Analysis of tumor-infiltrating CD103 resident memory T-cell content in recurrent laryngeal squamous cell carcinoma
      description:Recurrent laryngeal squamous cell carcinomas (LSCCs) are associated with poor outcomes, without reliable biomarkers to identify patients who may benefit from adjuvant therapies. Given the emergence of tumor-infiltrating lymphocytes (TIL) as a biomarker in head and neck squamous cell carcinoma, we generated predictive models to understand the utility of CD4+, CD8+ and/or CD103+ TIL status in patients with advanced LSCC. Tissue microarrays were constructed from salvage laryngectomy specimens of 183 patients with recurrent/persistent LSCC and independently stained for CD4+, CD8+, and CD103+ TIL content. Cox proportional hazards regression analysis was employed to assess combinations of CD4+, CD8+, and CD103+ TIL levels for prediction of overall survival (OS), disease-specific survival (DSS), and disease-free survival (DFS) in patients with recurrent/persistent LSCC. High tumor CD103+ TIL content was associated with significantly improved OS, DSS, and DFS and was a stronger predictor of survival in recurrent/persistent LSCC than either high CD8+ or CD4+ TIL content. On multivariate analysis, an “immune-rich” phenotype, in which tumors were enriched for both CD103+ and CD4+ TILs, conferred a survival benefit (OS hazard ratio: 0.28, p = 0.0014; DSS hazard ratio: 0.09, p = 0.0015; DFS hazard ratio: 0.18, p = 0.0018) in recurrent/persistent LSCC. An immune profile driven by CD103+ TIL content, alone and in combination with CD4+ TIL content, is a prognostic biomarker of survival in patients with recurrent/persistent LSCC. Predictive models described herein may thus prove valuable in prognostic stratification and lead to personalized treatment paradigms for this patient population.
      datePublished:2018-10-25T00:00:00Z
      dateModified:2018-10-25T00:00:00Z
      pageStart:213
      pageEnd:220
      sameAs:https://doi.org/10.1007/s00262-018-2256-3
      keywords:
         CD103
         Resident memory
         T-cell
         HNSCC
         Larynx
         Oncology
         Immunology
         Cancer Research
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      author:
            name:Jacqueline E. Mann
            affiliation:
                  name:University of Michigan
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                     type:PostalAddress
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            name:Joshua D. Smith
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            name:Andrew C. Birkeland
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                     name:Department of Otolaryngology - Head and Neck Surgery, University of Michigan, Ann Arbor, USA
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            type:Person
            name:Emily Bellile
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                  name:University of Michigan
                  address:
                     name:Department of Biostatistics, University of Michigan, Ann Arbor, USA
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            type:Person
            name:Paul Swiecicki
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                  name:University of Michigan
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            name:Michelle Mierzwa
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            name:Jonathan B. McHugh
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         name:Department of Otolaryngology - Head and Neck Surgery, University of Michigan, Ann Arbor, USA
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            address:
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               type:PostalAddress
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               type:PostalAddress
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            address:
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            address:
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               type:PostalAddress
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            name:University of Michigan
            address:
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               type:PostalAddress
            type:Organization
            name:University of Michigan
            address:
               name:Department of Pharmacology, University of Michigan, Ann Arbor, USA
               type:PostalAddress
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      name:Department of Otolaryngology - Head and Neck Surgery, University of Michigan, Ann Arbor, USA
      name:Department of Pathology, University of Michigan, Ann Arbor, USA
      name:Department of Otolaryngology - Head and Neck Surgery, University of Michigan, Ann Arbor, USA
      name:Department of Otolaryngology - Head and Neck Surgery, University of Michigan, Ann Arbor, USA
      name:Department of Biostatistics, University of Michigan, Ann Arbor, USA
      name:Department of Hematology and Oncology, University of Michigan, Ann Arbor, USA
      name:Department of Radiation Oncology, University of Michigan, Ann Arbor, USA
      name:Department of Otolaryngology - Head and Neck Surgery, University of Michigan, Ann Arbor, USA
      name:Department of Otolaryngology - Head and Neck Surgery, University of Michigan, Ann Arbor, USA
      name:Department of Otolaryngology - Head and Neck Surgery, University of Michigan, Ann Arbor, USA
      name:Department of Otolaryngology - Head and Neck Surgery, University of Michigan, Ann Arbor, USA
      name:Department of Otolaryngology - Head and Neck Surgery, University of Michigan, Ann Arbor, USA
      name:Department of Otolaryngology - Head and Neck Surgery, University of Michigan, Ann Arbor, USA
      name:Department of Otolaryngology - Head and Neck Surgery, University of Michigan, Ann Arbor, USA
      name:Rogel Cancer Center, University of Michigan, Ann Arbor, USA
      name:Department of Otolaryngology - Head and Neck Surgery, University of Michigan, Ann Arbor, USA
      name:Rogel Cancer Center, University of Michigan, Ann Arbor, USA
      name:Department of Otolaryngology - Head and Neck Surgery, University of Michigan, Ann Arbor, USA
      name:Rogel Cancer Center, University of Michigan, Ann Arbor, USA
      name:Department of Otolaryngology - Head and Neck Surgery, University of Michigan, Ann Arbor, USA
      name:Rogel Cancer Center, University of Michigan, Ann Arbor, USA
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      name:Department of Otolaryngology - Head and Neck Surgery, University of Michigan, Ann Arbor, USA
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      name:Department of Otolaryngology - Head and Neck Surgery, University of Michigan, Ann Arbor, USA
      name:Rogel Cancer Center, University of Michigan, Ann Arbor, USA
      name:Department of Pharmacology, University of Michigan, Ann Arbor, USA
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