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Ines Chevolet

Researcher at Ghent University Hospital

Publications -  22
Citations -  1061

Ines Chevolet is an academic researcher from Ghent University Hospital. The author has contributed to research in topics: Melanoma & Immune system. The author has an hindex of 14, co-authored 22 publications receiving 892 citations. Previous affiliations of Ines Chevolet include University of Zurich & Ghent University.

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The rationale of indoleamine 2,3-dioxygenase inhibition for cancer therapy.

TL;DR: Current available data on the role of IDO in cancer and the current results obtained with IDO inhibition are reviewed, both in animal models and in phase 1 and 2 clinical trials in humans.
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Combination of dabrafenib plus trametinib for BRAF and MEK inhibitor pretreated patients with advanced BRAFV600-mutant melanoma: an open-label, single arm, dual-centre, phase 2 clinical trial

TL;DR: Rechallenge with dabrafenib plus trametinib showed anti-tumour activity in patients who had previously progressed on BRAF inhibitors and as such, rechallenge represents a potential new treatment option for these patients.
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Quantitative assessment of BRAF V600 mutant circulating cell-free tumor DNA as a tool for therapeutic monitoring in metastatic melanoma patients treated with BRAF/MEK inhibitors

TL;DR: Quantitative analysis of BRAF V600mut ctDNA in plasma has unique features as a monitoring tool during treatment with BRAF/MEK inhibitors and its potential as an early predictor of acquired resistance deserves further evaluation.
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Characterization of the in vivo immune network of IDO, tryptophan metabolism, PD-L1, and CTLA-4 in circulating immune cells in melanoma

TL;DR: The expression of IDO, PD-L1, and CTLA-4 in the peripheral blood of melanoma patients is strongly interconnected, associated with advanced disease and negative outcome, independent of disease stage, and combination treatments targeting several of these markers are likely to exert a synergistic response.
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miR-145 overexpression suppresses the migration and invasion of metastatic melanoma cells.

TL;DR: Evidence is provided that miR-145 is an invasion suppressor in metastatic melanoma cells and may serve as a useful therapeutic agent in melanoma when re-expressed in situ, despite the fact that it remains unclear which genes or pathways are regulated by miRNAs in melanomas.