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. 2022 Mar 10;29(3):1902–1918. doi: 10.3390/curroncol29030155

Table 2.

Molecular profiling’s characteristics.

F1LCDx’s Characteristics Overall Population
n = 180
AMA
n = 100 (52%)
Non-AMA
n = 80 (42%)
p-Value *
Result Delay 0.56
  Median, days (range) 13 (5–38) 13 (5–28) 13 (7–27)
Timing of F1LCDx testing 0.0004
  Progression on non-TT 109 (61%) 74 (74%) 35 (44%)
  During treatment 44 (24%) 16 (16%) 28 (35%)
  Progression on TT 11 (6%) 6 (6%) 5 (6%)
  Diagnosis 7 (4%) 1 (1%) 6 (7%)
  Metastatic relapse 6 (3%) 2 (2%) 4 (5%)
  Other 3 (2%) 1 (1%) 2 (3%)
Previous Molecular Profile
  n (%) 147 (82%) 83 (83%) 64 (80%) -
  with previous MA 99/147 (67%) 60/83 (72%) 39/64 (61%) 0.7
  with previous AMA 53/147 (36%) 38/83 (46%) 15/64 (23%) 0.16
Tumor Fraction (%) 0.91
  Median (range) 21 (10–72) 21 (10–72) 19 (11–71)
Tumor Mutational Burden 0.01
  <10 mut/Mb 84 (47%) 43 (43%) 41 (51%)
  ≥10 mut/Mb 12 (6%) 11 (11%) 1 (1%)
  Missing 84 (47%) 46 (46%) 38 (48%)
MSI status 0.35
  MSI high 1 (1%) 1 (1%) 0
  MSI high not detected 28 (15%) 13 (13%) 15 (19%)
  Undetermined 151 (84%) 86 (86%) 65 (81%)

AMA: actionable molecular alteration; F1LCDx: FoundationOne Liquid CDx; MA: molecular alteration; MMT: molecularly matched therapy; TT: targeted therapy. * p-value is provided for comparison between groups: “AMA” vs. “non-AMA”.