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. 2018 Oct 2;92(1093):20180101. doi: 10.1259/bjr.20180101

Table 2.

Tumour visibility on DBT + FFDM and Clinicopathologic variables: Univariate analysis

Clinicopathologic variables Total (n = 106) Tumour visibility on DBT + FFDM
1 (n = 22) 2 (n = 11) 3 (n = 73) P-value a
Age (years)
 Mean ± SD 52.2 ± 11.4 (range 22–77) 47.6 ± 7.9 50.6 ± 8.2 53.9 ± 12.3 0.078
Tumour size(mm) b
 Mean ± SD 14.6 ± 4.6 (range 4–20) 12.7 ± 5.1 12.7 ± 3.4 14.1 ± 4.6 0.728
Tumour histology
 Ductal 97 (91.5) 18 (81.8) 11 (100.0) 68 (93.2) 0.396
 Lobular 5 (4.7) 2 (9.1) 0 (0) 3 (4.1)
 Others c 4 (3.8) 2 (9.1) 0 (0) 2 (2.7)
Histologic grade
 1or 2 55 (51.9) 13 (59.1) 7 (63.6) 35 (47.9) 0.468
 3 51 (48.1) 9 (40.9) 4 (36.4) 38 (52.1)
KI-67 (%)
 ≤14 95 (89.6) 20 (90.9) 11 (100) 64 (87.7) 0.222
 >14 11 (10.4) 2 (9.1) 0 (0) 9 (12.3)
IHC subtype
 ER-positive 86 (81.1) 20 (90.9) 9 (81.8) 57 (78.1) 0.318
 HER2-enriched 10 (9.4) 2 (9.1) 0 (0) 8 (11.0)
 Triple negative 10 (9.4) 0 (0) 2 (18.2) 8 (11.0)

DBT, digital breast tomosynthesis; FFDM, full-field digital mammography; SD, standard deviation; ER, estrogen receptor; HER2, human epidermal growth factor receptor 2; IHC, immuno histo chemistry.

Data are numbers of cases, and data in parentheses are percentages.

a

P-values were obtained by the Pearson’s Chi-square test or Fisher’s exact test for categorical variables and Mann-Whitney test for continuous variables. P-value < 0.050 was considered to indicate a statistically significant difference.

b

Determined by the greatest dimension of the invasive tumour on the basis of the surgically excised specimens.

c

Papillary (n = 2, 1.9%), mucinous (n = 1, 0.9%), and tubular (n = 1, 0.9%) cancers.