Table I.
Parameters (n=40) | Patient no. (%) |
---|---|
Age (years) | 64 (range, 44-88) |
Menopause | |
Post-/premenopausal | 34 (85.0)/6 (15.0) |
Degree of progression (metastasis) | |
Bone or soft tissue/visceral | 21 (52.5)/19 (47.5) |
Estrogen receptor | |
Strongly positive/weakly positive | 33 (82.5)/7 (17.5) |
Progesterone receptor | |
Strongly positive/weakly positive | 14 (35.0)/26 (65.0) |
HER2 | |
Negative/positive | 36 (90.0)/4 (10.0) |
Ki67 | |
≤14/>14% | 33 (82.5)/7 (17.5) |
Treatment | |
Letrozole/anastrozole/tamoxifen ± LHRH agonist/exemestane | 22 (55.0)/11 (27.5)/6 (15.0)/1 (2.5) |
Clinical response | |
CR/PR/SD ≥24 weeks/SD <24 weeks/PD | 0 (0.0)/30 (75.0)/4 (10.0)/2 (5.0)/4 (10.0) |
Clinical response | |
ORR/CBR/DCR | 30 (75.0)/30 (85.0)/4 (90.0) |
HER2, human epidermal growth factor receptor 2; LHRH, luteinizing hormone-releasing hormone; pCR, pathological complete response; CR, complete response; PR, partial response; SD, stable disease; PD, progressive disease; ORR, objective response rate; CBR, clinical benefit response; DCR, disease control rate.