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. 2024 Jul 19;18(10):2356–2368. doi: 10.1002/1878-0261.13698

Table 1.

Demographic and clinicopathologic features of endometrial cancers stratified by ERBB2 genetic alteration status. The number of cases in each category do not always sum up to the total number of cases in the cohort due to missing data values. amp, amplified; CN‐H/TP53abn, copy number‐high/TP53 abnormal; CN‐L/NSMP, copy number‐low/no specific molecular profile; FIGO, International Federation of Gynecology and Obstetrics; High‐grade EC‐NOS, high‐grade endometrial carcinoma, not otherwise specified; MSI‐H, microsatellite instability‐high; mut, mutated; non‐amp, non‐amplified; wt, wildtype.

Characteristic ERBB2 mutation/copy number status, N = 1859 P‐value a
wt/non‐amp, N = 1691, n (%) mut/non‐amp, N = 58, n (%) wt/amp, N = 99, n (%) mut/amp, N = 11, n (%) mut/non‐amp vs wt/non‐amp mut/non‐amp vs wt/amp
Age at diagnosis [median, years (range)] 63 (21–96) 60 (31–83) 66 (54–86) 70 (54–75) 0.041 < 0.001
BMI [median, kg·m−2, (range)] 29.7 (14.9–67.6) 28.0 (16.9–48.4) 28.3 (19.3–48.2) 29.3 (21.6–52.7) 0.08 0.95
Stage (FIGO 2009)
I 906 (59) 40 (71) 25 (29) 3 (33) 0.22 < 0.001
II 65 (4.2) 3 (5.4) 4 (4.7) 1 (11)
III 309 (20) 9 (16) 24 (28) 2 (22)
IV 251 (16) 4 (7.1) 32 (38) 3 (33)
Histologic type
Endometrioid 948 (56) 38 (66) 7 (7.1) 1 (9.1) 0.12 < 0.001
Serous 233 (14) 4 (6.9) 34 (34) 8 (73)
Clear cell 47 (2.8) 4 (6.9) 5 (5.1) 1 (9.1)
Carcinosarcoma 196 (12) 4 (6.9) 25 (25) 1 (9.1)
Mixed/high‐grade EC‐NOS 140 (8.3) 6 (10) 23 (23) 0 (0)
Undifferentiated/de‐differentiated 36 (2.1) 2 (3.4) 1 (1.0) 0 (0)
Unclassifiable 91 (5.4) 0 (0) 4 (4.0) 0 (0)
FIGO grade (for endometrioid only)
1 or 2 741 (81) 30 (79) 5 (71) 0 (0) 0.84 0.64
3 175 (19) 8 (21) 2 (29) 1 (100)
Molecular subtype
POLE 95 (5.6%) 6 (11%) 0 0 < 0.001 < 0.001
MSI‐H 404 (24%) 32 (59%) 0 0
CN‐L/NSMP 561 (33%) 7 (13%) 8 (8.1%) 1 (9.1%)
CN‐H/TP53abn 631 (37%) 9 (17%) 91 (92%) 10 (91%)
a

Fisher exact test, two‐tailed.