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. 2021 Oct 27;10(11):e1351. doi: 10.1002/cti2.1351

Table 2.

TCR sequencing results in the tumor tissue, pre‐therapy and post‐cycle #4 blood samples

Sample DNA input (ng) Total productive sequences Unique productive sequences CumFreq‐100 (%) CumFreq‐25 (%) Max‐Freq (%) Productive clonality
Tumor tissue 1611 (320–10 064) 5400 (603–48 501) 3172 (447–19 934) 23.16 (3.82–66.67) 11.10 (1.49–57.69) 1.55 (0.12–10.26) 0.048 (0.007–0.296)
PBMC Pre‐Rx 2495 (1240–2535) 46 512 (1 1189–218 764) 29 048 (7231–87 967) 19.31 (0.23–68.04) 15.09 (0.09–63.49) 3.02 (0.25–33.84) 0.09 (0.01–0.47)
PBMC post‐cycle #4 2493 (976–2520) 80 012 (1067–201 848) 27 799 (930–89 150) 18.30 (0.02–84.32) 12.36 (0.02–77.53) 2.56 (0.3–40.69) 0.10 (0.01–0.54)

Values are expressed as median (range).

CumFeq‐25, that of the most dominant 25 clonotypes; CumFreq‐100, the cumulative frequencies of the most dominant 100 clonotypes; Max‐Freq, the frequency of the most dominant clonotype, PBMC post‐cycle #4, peripheral blood mononuclear cells after four cycles of R‐CHOP; PBMC Pre‐Rx, peripheral blood mononuclear cells at diagnosis.