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Perspectives in melanoma: meeting report from the Melanoma Bridge (November 29th-1 December 1st, 2018, Naples, Italy).
Ascierto, Paolo A; Agarwala, Sanjiv S; Botti, Gerardo; Budillon, Alfredo; Davies, Michael A; Dummer, Reinhard; Ernstoff, Marc; Ferrone, Soldano; Formenti, Silvia; Gajewski, Thomas F; Garbe, Claus; Hamid, Omid; Lo, Roger S; Luke, Jason J; Michielin, Oliver; Palmieri, Giuseppe; Zitvogel, Laurence; Marincola, Francesco M; Masucci, Giuseppe; Caracò, Corrado; Thurin, Magdalena; Puzanov, Igor.
Afiliação
  • Ascierto PA; Unit of Melanoma, Cancer Immunotherapy and Innovative Therapy, Istituto Nazionale Tumori IRCCS Fondazione "G. Pascale", Via Mariano Semmola, 80131, Naples, Italy. paolo.ascierto@gmail.com.
  • Agarwala SS; Medical Oncology and Hematology, St. Luke's University Hospital and Temple University, Bethlehem, PA, USA.
  • Botti G; Istituto Nazionale Tumori-IRCCS Fondazione "G. Pascale", Naples, Italy.
  • Budillon A; Experimental Pharmacology Unit, Department of Translational Research, Istituto Nazionale Tumori-IRCCS Fondazione "G. Pascale", Naples, Italy.
  • Davies MA; Department of Melanoma Medical Oncology, Department of Systems Biology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Dummer R; Department of Dermatology, University of Zurich Hospital, Zurich, Switzerland.
  • Ernstoff M; Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
  • Ferrone S; Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
  • Formenti S; Weill Cornell Medical College, New York Presbyterian Hospital, New York, NY, USA.
  • Gajewski TF; Department of Pathology and Department of Medicine, Section of Hematology/Oncology, The University of Chicago Medicine, Chicago, IL, USA.
  • Garbe C; Division of Dermatologic Oncology, Department of Dermatology, Eberhard Karls University, Tuebingen, Germany.
  • Hamid O; The Angeles Clinic, Experimental Therapeutics Cedars Sinai Foundation, Los Angeles, CA, USA.
  • Lo RS; Jonsson Comprehensive Cancer Center, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
  • Luke JJ; University of Chicago Medical Center, Chicago, IL, USA.
  • Michielin O; Oncology Department, UNIL-CHUV, Lausanne, Switzerland.
  • Palmieri G; Unit of Cancer Genetics, Institute of Biomolecular Chemistry, National Research Council, Sassari, Italy.
  • Zitvogel L; Institut de Cancérologie, Gustave Roussy Cancer Campus, Villejuif, Paris, France.
  • Marincola FM; Refuge Biotechnologies, Menlo Park, CA, USA.
  • Masucci G; Department of Oncology-Pathology, Karolinska Institute, Stockholm, Sweden.
  • Caracò C; Division of Surgery of Melanoma and Skin Cancer, Istituto Nazionale Tumori-IRCCS Fondazione "G. Pascale", Naples, Italy.
  • Thurin M; Cancer Diagnosis Program, Division of Cancer Treatment and Diagnosis, NCI, 9609 Medical Center Drive, Bethesda, MD, 20892-7420, USA. thurinm@mail.nih.gov.
  • Puzanov I; Department of Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
J Transl Med ; 17(1): 234, 2019 07 22.
Article em En | MEDLINE | ID: mdl-31331337
ABSTRACT
Diagnosis of melanocytic lesions, correct prognostication of patients, selection of appropriate adjuvant and systemic therapies, and prediction of response to a given therapy remain very real challenges in melanoma. Recent studies have shown that immune checkpoint blockade that represents a forefront in cancer therapy, provide responses but they are not universal. Improved understanding of the tumor microenvironment, tumor immunity and response to therapy has prompted extensive translational and clinical research in melanoma. Development of novel biomarker platforms may help to improve diagnostics and predictive accuracy for selection of patients for specific treatment. There is a growing evidence that genomic and immune features of pre-treatment tumor biopsies may correlate with response in patients with melanoma and other cancers they have yet to be fully characterized and implemented clinically. For example, advancements in sequencing and the understanding of the tumor microenvironment in melanoma have led to the use of genome sequencing and gene expression for development of multi-marker assays that show association with inflammatory state of the tumor and potential to predict response to immunotherapy. As such, melanoma serves as a model system for understanding cancer immunity and patient response to immunotherapy, either alone or in combination with other treatment modalities. Overall, the aim for the translational and clinical studies is to achieve incremental improvements through the development and identification of optimal treatment regimens, which increasingly involve doublet as well as triplet combinations, as well as through development of biomarkers to improve immune response. These and other topics in the management of melanoma were the focus of discussions at the fourth Melanoma Bridge meeting (November 29th-December 1st, 2018, Naples, Italy), which is summarised in this report.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Melanoma Tipo de estudo: Prognostic_studies Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Melanoma Tipo de estudo: Prognostic_studies Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2019 Tipo de documento: Article