TY - JOUR
T1 - Molecular analysis of primary melanoma T cells identifies patients at risk for metastatic recurrence
AU - Pruessmann, Wiebke
AU - Rytlewski, Julie
AU - Wilmott, James
AU - Mihm, Martin C.
AU - Attrill, Grace H.
AU - Dyring-Andersen, Beatrice
AU - Fields, Paul
AU - Zhan, Qian
AU - Colebatch, Andrew J.
AU - Ferguson, Peter M.
AU - Thompson, John F.
AU - Kallenbach, Klaus
AU - Yusko, Erik
AU - Clark, Rachael A.
AU - Robins, Harlan
AU - Scolyer, Richard A.
AU - Kupper, Thomas S.
N1 - Publisher Copyright:
© 2020, The Author(s), under exclusive licence to Springer Nature America, Inc.
PY - 2020/2/1
Y1 - 2020/2/1
N2 - Primary melanomas >1 mm thickness are potentially curable by resection, but can recur metastatically. We assessed the prognostic value of the T-cell fraction (TCFr) and repertoire T-cell clonality, measured by high-throughput sequencing of the T-cell receptor β-chain in T2–T4 primary melanomas (n = 199). TCFr accurately predicted progression-free survival and was independent of thickness, ulceration, mitotic rate and age. TCFr was second only to tumor thickness in its predictive value, using a gradient-boosted model. For accurate progression-free survival 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. The present study suggests that a successful T-cell-mediated, antitumour response can be present in primary melanomas.
AB - Primary melanomas >1 mm thickness are potentially curable by resection, but can recur metastatically. We assessed the prognostic value of the T-cell fraction (TCFr) and repertoire T-cell clonality, measured by high-throughput sequencing of the T-cell receptor β-chain in T2–T4 primary melanomas (n = 199). TCFr accurately predicted progression-free survival and was independent of thickness, ulceration, mitotic rate and age. TCFr was second only to tumor thickness in its predictive value, using a gradient-boosted model. For accurate progression-free survival 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. The present study suggests that a successful T-cell-mediated, antitumour response can be present in primary melanomas.
UR - http://www.scopus.com/inward/record.url?scp=85090028300&partnerID=8YFLogxK
U2 - 10.1038/s43018-019-0019-5
DO - 10.1038/s43018-019-0019-5
M3 - Journal articles
AN - SCOPUS:85090028300
SN - 2662-1347
VL - 1
SP - 197
EP - 209
JO - Nature Cancer
JF - Nature Cancer
IS - 2
ER -