Skip to main content

Table 1 Patient and tumor characteristics in all patients

From: Heregulin (HRG) assessment for clinical trial eligibility testing in a molecular registry (PRAEGNANT) in Germany

Characteristic

SHERBOC no(n = 525)

SHERBOC yes(n = 125)

Age at study entry (years)

60.9 (13.1)

61.1 (11.9)

BMI (kg/m2)

26.6 (5.9)

26.0 (5.6)

Time from diagnosis to metastasis (years)

6.0 (6.5)

6.9 (7.5)

Tumor grade

 1

38 (7.8)

13 (12.5)

 2

333 (68.4)

75 (72.1)

 3

116 (23.8)

16 (15.4)

ECOG score

 0

251 (50.3)

82 (67.8)

 1

192 (38.5)

33 (27.3)

  ≥ 2

56 (11.2)

6 (5.0)

Concomitant diseases

 0 or 1

242 (46.4)

62 (50.4)

 2 to 4

192 (36.8)

46 (37.4)

  ≥ 5

88 (16.9)

15 (12.2)

Metastasis pattern

 Brain

48 (9.2)

4 (3.3)

 Visceral

237 (45.3)

42 (34.1)

 Bone

88 (16.8)

29 (23.6)

 Other

150 (28.7)

48 (39.0)

HRG test

 Negative

–

18 (47.4)a

 Positive

–

14 (36.8)a

 Not evaluable

–

6 (15.8)a

Ever received chemotherapy

 No

279 (53.1)

125 (100.0)

 Yes

246 (46.9)

0 (0.0)

Ever received endocrine therapy

 No

109 (20.8)

12 (9.6)

 Yes

416 (79.2)

113 (90.4)

Ever received fulvestrant

 No

356 (67.8)

125 (100.0)

 Yes

169 (32.2)

0 (0.0)

Previous CDK4/6i documented

 No

405 (77.1)

4 (3.2)b

 Yes

120 (22.9)

121 (96.8)

SHERBOC line

 1

290 (55.2)

117 (93.6)

 2

235 (44.8)

8 (6.4)

  1. BMI Body mass index; ECOG Eastern Cooperative Oncology Group; HRG Heregulin. CDK4/6i CDK4/6 inhibitor
  2. Means and standard deviation (SD) are shown for continuous characteristics, and frequency and percentage for categorical characteristics
  3. a Percentages refer only to the 38 patients for whom a testing was done. For the rest of the population no test results are available due to the early termination of the trial
  4. bThese patients were confirmed to be clinically eligible for SHERBOC despite CDK4/6i was not documented yet at time of database closure