Increased frequency and number of KLL-specific clonotypes in tumors is associated with improved MCC-specific survival. Increased frequency and number of.

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Increased frequency and number of KLL-specific clonotypes in tumors is associated with improved MCC-specific survival. Increased frequency and number of KLL-specific clonotypes in tumors is associated with improved MCC-specific survival. A, MCC-specific survival was significantly increased for patients who had higher (n = 9) versus lower (n = 2) percentage of KLL-specific T cells in tumor (1.9%–18% vs. 0%–0.14%, P = 0.0009 by the log-rank test). B, MCC-specific survival was increased for patients who had many unique KLL-specific clonotypes (5–108 clonotypes, n = 7 patients) in their tumors, compared with patients with few KLL-specific clonotypes (0–3, n = 4; P = 0.0051 by the log-rank test). C, Patients were grouped by whether they developed metastatic disease (n = 7) or remained disease-free after definitive treatment of first presentation of disease (n = 3). The percentage of KLL-specific T cells tended to be higher in patients without recurrence (range, 4.3%–18%) than in those who developed metastatic disease (range, 0%–10.8%, P =0.11). D, The number of KLL-specific clonotypes was significantly higher in patients without recurrence (median, 38; range, 9–108) compared with those who developed metastatic disease (median, 2; range, 0–17, P = 0.02). Natalie J. Miller et al. Cancer Immunol Res 2017;5:137-147 ©2017 by American Association for Cancer Research