| Literature DB >> 33305293 |
Wiebke Pruessmann1,2, Julie Rytlewski3, James Wilmott4, Richard A Scolyer4,5, Thomas S Kupper6, Martin C Mihm1, Grace H Attrill4, Beatrice Dyring-Andersen1,7, Paul Fields3, Qian Zhan1, Andrew J Colebatch4,5, Peter M Ferguson4,5, John F Thompson4,8, Klaus Kallenbach9, Erik Yusko3, Rachael A Clark1, Harlan Robins3,10.
Abstract
Primary melanomas >1 mm thickness are potentially curable by resection, but can recur metastatically. We assessed the prognostic value of T cell fraction (TCFr) and repertoire T cell clonality, measured by high-throughput-sequencing of the T cell receptor beta chain (TRB) in T2-T4 primary melanomas (n=199). TCFr accurately predicted progression-free survival (PFS) and was independent of thickness, ulceration, mitotic rate, or age. TCFr was second only to tumor thickness in its predictive value, using a gradient boosted model. For accurate PFS prediction, adding TCFr to tumor thickness was superior to adding any other histopathological variable. Furthermore, a TCFr >20% was protective regardless of tumor ulceration status, mitotic rate or presence of nodal disease. TCFr is a quantitative molecular assessment that predicts metastatic recurrence in primary melanoma patients whose disease has been resected surgically. This study suggests that a successful T cell-mediated antitumor response can be present in primary melanomas.Entities:
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Year: 2020 PMID: 33305293 PMCID: PMC7725220 DOI: 10.1038/s43018-019-0019-5
Source DB: PubMed Journal: Nat Cancer ISSN: 2662-1347