Skip to main content
. 2020 Apr 28;25(11):927–936. doi: 10.1634/theoncologist.2019-0561

Table 1.

Patient demographic and disease characteristics at baseline

Characteristics Patients (n = 36) %
Median age (range), years 55.5 (31–78)
Menopausal status
Premenopausal a 8 22.2
Postmenopausal 28 77.8
Disease‐free interval, years b
>5 18 50.0
≤5 7 19.4
Pathologic type
Invasive ductal carcinoma 33 91.7
Invasive lobular carcinoma 2 5.6
Tubular carcinoma 1 2.7
PgR status
Positive 32 88.9
Negative 4 11.1
Metastatic sites
Nonvisceral 21 58.3
Bone 23 63.9
Bone‐only 2 5.6
Visceral disease 15 41.7
Any lung 11 30.6
Pleural 5 13.9
Peritoneum 1 2.8
No. of disease sites
1–3 9 25.0
4–6 9 25.0
7–9 7 19.4
≥10 11 30.6
De novo metastatic disease 11 30.6
Adjuvant ET
Antiestrogen 14 38.9
Aromatase inhibitor 4 11.1
Antiestrogen followed by aromatase inhibitor 2 5.6
None 5 13.9
Prior ET for metastatic disease
None 27 75.0
Yes 9 25.0
Prior ET type for metastatic disease
Antiestrogen ± LH‐RH analog 1 2.8
Aromatase inhibitor ± LH‐RH analog 8 22.2
Prior sensitivity to ET
Primary resistance 1 2.7
Secondary resistance 23 63.8
Prior chemotherapy for metastatic disease
None 31 86.1
Yes 5 13.9
Treatment immediately preceding fulvestrant
None 12 33.3
Chemotherapy 4 11.1
Antiestrogen 7 19.4
Aromatase inhibitor 13 36.1
Progression‐free survival
Events 19 (range 1.8–28.0 months) 52.8
Censored 17 (range 5.6–19.4 months) 47.2
With negative 18F‐FES lesions
None 26 72.2
Yes 10 27.8
a

For premenopausal women, fulvestrant was given upon the administration of gonadotropin‐releasing hormone agonist.

b

Patients with stage IV breast cancer at initial diagnosis were excluded (n = 11).

Abbreviations: ER, estrogen receptor; ET, endocrine therapy; FES, fluoroestradiol; LH‐RH, luteinizing hormone releasing hormone; PgR, progesterone receptor.