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      The biology and treatment of Merkel cell carcinoma: current understanding and research priorities

      review-article
      1 , 2 , 3 , 4 , 5 , 6 , 7 , , on behalf of the International Workshop on Merkel Cell Carcinoma Research (IWMCC) Working Group
      Nature Reviews. Clinical Oncology
      Nature Publishing Group UK
      Neuroendocrine cancer, Skin cancer, Cancer immunotherapy, Targeted therapies

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          Abstract

          Merkel cell carcinoma (MCC) is a rare and aggressive skin cancer associated with advanced age and immunosuppression. Over the past decade, an association has been discovered between MCC and either integration of the Merkel cell polyomavirus, which likely drives tumorigenesis, or somatic mutations owing to ultraviolet-induced DNA damage. Both virus-positive and virus-negative MCCs are immunogenic, and inhibition of the programmed cell death protein 1 (PD-1)–programmed cell death 1 ligand 1 (PD-L1) immune checkpoint has proved to be highly effective in treating patients with metastatic MCC; however, not all patients have a durable response to immunotherapy. Despite these rapid advances in the understanding and management of patients with MCC, many basic, translational and clinical research questions remain unanswered. In March 2018, an International Workshop on Merkel Cell Carcinoma Research was held at the US National Cancer Institute, at which academic, government and industry experts met to identify the highest-priority research questions. Here, we review the biology and treatment of MCC and report the consensus-based recommendations agreed upon during the workshop.

          Abstract

          Merkel cell carcinoma (MCC) is a rare and aggressive form of nonmelanoma skin cancer. The availability of immune checkpoint inhibition has improved the outcomes of a subset of patients with MCC, although many unmet needs continue to exist. In this Consensus Statement, the authors summarize developments in our understanding of MCC while also providing consensus recommendations for future research.

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          Most cited references148

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          Clinical characteristics of Merkel cell carcinoma at diagnosis in 195 patients: the AEIOU features.

          Merkel cell carcinoma (MCC) is an aggressive skin cancer with a mortality of 33%. Advanced disease at diagnosis is a poor prognostic factor, suggesting that earlier detection may improve outcome. No systematic analysis has been published to define the clinical features that are characteristic of MCC. We sought to define the clinical characteristics present at diagnosis to identify features that may aid clinicians in recognizing MCC. We conducted a cohort study of 195 patients given the diagnosis of MCC between 1980 and 2007. Data were collected prospectively in the majority of cases, and medical records were reviewed. An important finding was that 88% of MCCs were asymptomatic (nontender) despite rapid growth in the prior 3 months (63% of lesions) and being red or pink (56%). A majority of MCC lesions (56%) were presumed at biopsy to be benign, with a cyst/acneiform lesion being the single most common diagnosis (32%) given. The median delay from lesion appearance to biopsy was 3 months (range 1-54 months), and median tumor diameter was 1.8 cm. Similar to earlier studies, 81% of primary MCCs occurred on ultraviolet-exposed sites, and our cohort was elderly (90% >50 years), predominantly white (98%), and often profoundly immune suppressed (7.8%). An additional novel finding was that chronic lymphocytic leukemia was more than 30-fold overrepresented among patients with MCC. The study was limited to patients seen at a tertiary care center. Complete clinical data could not be obtained on all patients. This study could not assess the specificity of the clinical characteristics of MCC. To our knowledge, this study is the first to define clinical features that may serve as clues in the diagnosis of MCC. The most significant features can be summarized in an acronym: AEIOU (asymptomatic/lack of tenderness, expanding rapidly, immune suppression, older than 50 years, and ultraviolet-exposed site on a person with fair skin). In our series, 89% of primary MCCs had 3 or more of these findings. Although MCC is uncommon, when present in combination, these features may indicate a concerning process that would warrant biopsy. In particular, a lesion that is red and expanding rapidly yet asymptomatic should be of concern.
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            PD-L1 expression in the Merkel cell carcinoma microenvironment: association with inflammation, Merkel cell polyomavirus and overall survival.

            Merkel cell carcinoma (MCC) is a lethal, virus-associated cancer that lacks effective therapies for advanced disease. Agents blocking the PD-1/PD-L1 pathway have demonstrated objective, durable tumor regressions in patients with advanced solid malignancies and efficacy has been linked to PD-L1 expression in the tumor microenvironment. To investigate whether MCC might be a target for PD-1/PD-L1 blockade, we examined MCC PD-L1 expression, its association with tumor-infiltrating lymphocytes (TILs), Merkel cell polyomavirus (MCPyV), and overall survival. Sixty-seven MCC specimens from 49 patients were assessed with immunohistochemistry for PD-L1 expression by tumor cells and TILs, and immune infiltrates were characterized phenotypically. Tumor cell and TIL PD-L1 expression were observed in 49% and 55% of patients, respectively. In specimens with PD-L1(+) tumor cells, 97% (28/29) demonstrated a geographic association with immune infiltrates. Among specimens with moderate-severe TIL intensities, 100% (29/29) demonstrated PD-L1 expression by tumor cells. Significant associations were also observed between the presence of MCPyV DNA, a brisk inflammatory response, and tumor cell PD-L1 expression: MCPyV(-) tumor cells were uniformly PD-L1(-). Taken together, these findings suggest that a local tumor-specific and potentially MCPyV-specific immune response drives tumor PD-L1 expression, similar to previous observations in melanoma and head and neck squamous cell carcinomas. In multivariate analyses, PD-L1(-) MCCs were independently associated with worse overall survival (hazard ratio 3.12; 95% CI, 1.28-7.61; p=0.012). These findings suggest that an endogenous immune response promotes PD-L1 expression in the MCC microenvironment when MCPyV is present, and provide a rationale for investigating therapies blocking PD-1/PD-L1 for patients with MCC.
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              Merkel cell carcinoma: Current US incidence and projected increases based on changing demographics

              Background Merkel cell carcinoma (MCC) incidence rates are rising and strongly age-associated, relevant for an aging population. Objective Determine MCC incidence in the United States and project incident cases through the year 2025. Methods Registry data were obtained from the SEER-18 database, containing 6,600 MCC cases. Age and sex-adjusted projections were generated utilizing US census data. Results Between 2000–2013, there was a 95% increase in the number of reported MCC cases, compared to 57% for melanoma and 15% for all ‘solid’ cancers. In 2013, the MCC incidence rate was 0.7 per 100,000 person-years in the US, corresponding to 2,488 cases. MCC incidence increased exponentially with age, from 0.1 to 1.0 to 9.8 (per 100,000 person-years) between age groups 40–44, 60–64, 85+ years, respectively. Due to aging of the “baby-boom” generation, US MCC incidence is predicted to climb to 2,835 cases in 2020 and 3,284 cases in 2025. Limitations Projections assume the age-adjusted incidence rate stabilizes and thus may be underestimates. Conclusions An aging population is driving brisk increases in the number of new MCC cases in the US. This growing impact combined with a rapidly evolving therapeutic landscape warrants expanded awareness of MCC diagnosis and management.
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                Author and article information

                Contributors
                isaac.brownell@nih.gov
                Journal
                Nat Rev Clin Oncol
                Nat Rev Clin Oncol
                Nature Reviews. Clinical Oncology
                Nature Publishing Group UK (London )
                1759-4774
                1759-4782
                4 October 2018
                4 October 2018
                2018
                : 15
                : 12
                : 763-776
                Affiliations
                [1 ]ISNI 0000000086837370, GRID grid.214458.e, Department of Pathology, , University of Michigan Medical School, ; Ann Arbor, MI USA
                [2 ]ISNI 0000000086837370, GRID grid.214458.e, Department of Dermatology, , University of Michigan Medical School, ; Ann Arbor, MI USA
                [3 ]ISNI 0000 0004 1936 9000, GRID grid.21925.3d, Cancer Virology Program, , University of Pittsburgh, ; Pittsburgh, PA USA
                [4 ]ISNI 0000 0001 2106 9910, GRID grid.65499.37, Department of Medical Oncology, , Dana-Farber Cancer Institute, ; Boston, MA USA
                [5 ]ISNI 0000000122986657, GRID grid.34477.33, Department of Medicine, Division of Dermatology, , University of Washington, ; Seattle, WA USA
                [6 ]ISNI 0000 0001 2291 4776, GRID grid.240145.6, Department of Melanoma Medical Oncology, Division of Cancer Medicine, , MD Anderson Cancer Center, ; Houston, TX USA
                [7 ]ISNI 0000 0001 2297 5165, GRID grid.94365.3d, Dermatology Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) and National Cancer Institute (NCI), , NIH, ; Bethesda, MD USA
                Author information
                http://orcid.org/0000-0002-0802-2883
                http://orcid.org/0000-0002-0896-167X
                http://orcid.org/0000-0002-0090-9914
                Article
                103
                10.1038/s41571-018-0103-2
                6319370
                30287935
                63d98180-e5c5-42bb-963b-142e914434b9
                © Springer Nature Limited 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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                Consensus Statement
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                © Springer Nature Limited 2018

                neuroendocrine cancer,skin cancer,cancer immunotherapy,targeted therapies

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