Table 1.
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 |
For premenopausal women, fulvestrant was given upon the administration of gonadotropin‐releasing hormone agonist.
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.