Evidence map›Paper›PMID 34193182›Full record

ArticleJournal of translational medicine2021

Perspectives in Melanoma: meeting report from the Melanoma Bridge (December 3rd-5th, 2020, Italy).

Paolo A Ascierto, Christian Blank, Reinhard Dummer, Marc S Ernstoff, Soldano Ferrone, Bernard A Fox, Thomas F Gajewski, Claus Garbe, Patrick Hwu, Pawel Kalinski and 13 more

Open access · goldAbstract readConference Proceedings
In one paragraph

Article in Journal of translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 55% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 17 institutions in 7 countries.

Paolo A AsciertoDepartment of Melanoma, Cancer Immunotherapy and Innovative Therapy, Instituto Nazionale Tumori IRCCS "Fondazione G. Pascale", Naples, Italy. paolo.ascierto@gmail.com.ORCID 0000-0002-8322-475X
Christian BlankNetherlands Cancer Institute, Amsterdam, The Netherlands.
Reinhard DummerDepartment of Dermatology, University of Zurich Hospital, Zurich, Switzerland.
Marc S ErnstoffDevelopmental Therapeutics Program, Division of Cancer Therapy & Diagnosis, NCI, NIH, Bethesda, MD, USA.
Soldano FerroneDepartment of Surgery Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Bernard A FoxEarle A. Chiles Research Institute, Robert W. Franz Cancer Center, Providence Cancer Institute, Portland, OR, USA.
Thomas F GajewskiDepartment of Pathology and Department of Medicine (Section of Hematology/Oncology), University of Chicago, Chicago, IL, USA.
Claus GarbeCenter for Dermato-Oncology, University-Department of Dermatology, Tuebingen, Germany.
Patrick HwuMoffitt Cancer Center, Tampa, FL, USA.
Pawel KalinskiCancer Vaccine and Dendritic Cell Therapies, Center for Immunotherapy, Roswell Park Comprehensive Cancer Center, Developmental Therapeutics, Buffalo, NY, USA.
Michelle KrogsgaardMedical School, New York University Langone, New York, NY, USA.
Roger S LoJonsson Comprehensive Cancer Center David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Jason J LukeCancer Immunotherapeutic Center of UPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, PA, USA.
Bart NeynsMedical Oncology, Universitair Ziekenhuis Brussel, Brussels, Belgium.
Michael A PostowMemorial Sloan Kettering Cancer Center, New York, NY, USA.
Sergio A QuezadaCancer Immunology Unit, Research Department of Hematology, University College London Cancer Institute, London, UK.
Michele W L TengQIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Giorgio TrinchieriLaboratory of Integrative Cancer Immunology (LICI), Center for Cancer Research, NCI, NIH, Bethesda, MD, USA.
Alessandro TestoriImage Rigenerative Clinic-Skin Oncology Division, Milan, Italy.
Corrado CaracòDivision of Surgery of Melanoma and Skin Cancer, Istituto Nazionale Tumori "Fondazione Pascale" IRCCS, Naples, Italy.
Iman OsmanNew York University Langone Medical Center, New York, NY, USA.
Igor PuzanovDepartment of Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
Magdalena ThurinCancer Diagnosis Program, Division of Cancer Treatment and Diagnosis, NCI, NIH, Rockville, MD, USA.
Center for Cancer Research · USIstituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITNYU Langone Health · USRoswell Park Comprehensive Cancer Center · USEuropean Organisation for Research and Treatment of Cancer · BEHarvard University · USLondon Cancer · GBMemorial Sloan Kettering Cancer Center · USMoffitt Cancer Center · USProvidence Portland Medical Center · USQIMR Berghofer Medical Research Institute · AUThe Netherlands Cancer Institute · NLUCLA Jonsson Comprehensive Cancer CenterUniversitair Ziekenhuis Brussel · BEUniversity of Chicago · USUniversity of Pittsburgh · USUniversity of Zurich · CH

Funding

Cancer Research UK 20764Cancer Research UK 22246
6 · The paper itself

Abstract

Advances in immune checkpoint therapy and targeted therapy have led to improvement in overall survival for patients with advanced melanoma. Single agent checkpoint PD-1 blockade and combination with BRAF/MEK targeted therapy demonstrated benefit in overall survival (OS). Superior response rates have been demonstrated with combined PD-1/CTLA-4 blockade, with a significant OS benefit compared with single-agent PD-1 blockade. Despite the progress in diagnosis of melanocytic lesions, correct classification of patients, selection of appropriate adjuvant and systemic therapies, and prediction of response to therapy remain real challenges in melanoma. 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 but they have yet to be fully characterized and implemented clinically. Overall, the progress in melanoma therapeutics and translational research will help to optimize treatment regimens to overcome resistance and develop robust biomarkers to guide clinical decision-making. During the Melanoma Bridge meeting (December 3rd-5th, 2020, Italy) we reviewed the currently approved systemic and local therapies for advanced melanoma and discussed novel biomarker strategies and advances in precision medicine.

Indexed as

ImmunotherapyMelanomaHumansItalyMolecular Targeted TherapyTumor MicroenvironmentAdjuvantAnti-CTLA-4Anti-PD-1BiomarkersBRAF inhibitorCombination strategiesImmunotherapyMEK inhibitorMelanomaNeoadjuvantTarget therapy

Identifiers

PMID34193182
PMCPMC8243582
OpenAlexW3174692804

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.