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. 2020 Mar 7;10(3):415. doi: 10.3390/biom10030415

Table 4.

Comparison clinicopathological characteristics of high-grade serous ovarian carcinomas (HGSOC) patients with and without serum tumor-specific TP53 mutation at diagnosis.

HGSOC Patients Serum cfDNA at Diagnosis:
Without Tumor-Cpecific TP53 Mutation With Tumor-Specific TP53 Mutation p-Value
Number of patients 8 9
Average TP53 mutation allele frequency (MAF in %):
in tumor tissue 58% 62% 0.819
in cfDNA 0% 7% 0.115
NGS workflow (N):
I 4 4 0.819
II 4 5
Age at diagnosis (average):
57 55 0.703
FIGO Stage (N):
IC 1 0 0.024
IIIC 6 2
IV 1 7
Debulking surgery (N):
PDS 4 3 0.614
IDS 4 5
Residual Disease (N):
0–1 cm (optimal debulking) 6 5 0.402
1 cm or more (non-optimal debulking) 2 5
Progression-Free Survival (PFS):
0–6 months (n) 1 3 0.312
>6 months (n) 7 6
average cfDNA yield (ng/mL serum):
at diagnosis 129 95 0.363
after chemotherapy 31 45 0.106
at progression 117 45 0.268
TP53 mutation at progression measured by dPCR (N):
Yes 1 4 0.079
No 1 0
Other gene mutations detected in cfDNA at diagnosis:
PIK3CA p.H1047R 1.30%
ESR1 p.R394S 0.30%
TP53 p.T253I * 0.10%

PDS = primary Debulking surgery, IDS = interval Debulking surgery, NGS = next generation sequencing, dPCR = digital PCR, N = number of patients, * = TP53 p.T253I was identified in serum but not in tumor tissue.