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Giuseppe Masucci

Researcher at Karolinska Institutet

Publications -  137
Citations -  10026

Giuseppe Masucci is an academic researcher from Karolinska Institutet. The author has contributed to research in topics: Antigen & Cytotoxic T cell. The author has an hindex of 44, co-authored 133 publications receiving 8766 citations. Previous affiliations of Giuseppe Masucci include German Cancer Research Center & Karolinska University Hospital.

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International validation of the consensus Immunoscore for the classification of colon cancer: a prognostic and accuracy study

Franck Pagès, +120 more
- 26 May 2018 - 
TL;DR: The immunoscore provides a reliable estimate of the risk of recurrence in patients with colon cancer and supports the implementation of the consensus Immunoscore as a new component of a TNM-Immune classification of cancer.
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Towards the introduction of the 'Immunoscore' in the classification of malignant tumours.

Jérôme Galon, +56 more
TL;DR: In colorectal cancer, the Immunoscore may add to the significance of the current AJCC/UICC TNM classification, since it has been demonstrated to be a prognostic factor superior to the AJCC or UICCTNM classification.
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Cancer classification using the Immunoscore: a worldwide task force

Jérôme Galon, +68 more
TL;DR: Evidence supports the notion to include immunological biomarkers, implemented as a tool for the prediction of prognosis and response to therapy, into traditional classification of cancer, designated TNM-I (TNM-Immune), and introduction of this parameter as a biomarker to classify cancers will facilitate clinical decision-making.
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Immature Immunosuppressive CD14+HLA-DR−/low Cells in Melanoma Patients Are Stat3hi and Overexpress CD80, CD83, and DC-Sign

TL;DR: Examination of circulating CD14(+)HLA-DR(-/low) MDSC in 34 advanced malignant melanoma patients finds the coexpression of markers associated with mature phenotype and several observations suggest a redox imbalance in M DSC and indicate an important role of Stat3-dependent oxidative stress in MDSc-mediated T-cell suppression.