Table 2.
Pretreatment assessment Variable | Patients Treated with Bevacizumab Plus Letrozole (n=112) |
|||
---|---|---|---|---|
# of Patients (%) |
Mean ± Standard Deviation |
Median (Range) |
||
OARS IADLa | Completely Independent | 76 (67.9%) | 13.2 ± 1.5 | 32 (6–32) |
OARS Comorbidity | 0 1 2 or more |
76 (67.9%) 19 (17.0%) 17 (15.2%) |
||
MOSb | Activities of Daily Living | 76.8 ± 26.5 | 90 (5–100) | |
Social Activity | 47.9 ± 9.6 | 50 (25–75) | ||
Timed Up and Go | Seconds | 13.0 ± 9.2 | 10 (2–60) | |
Falls in past 6 months | None 1 or more Unavailable |
88 (78.6%) 22 (19.6%) 2 (1.8%) |
||
Hearing |
Excellent/Good Fair/Poor/Deaf Unavailable |
97 (86.6%) 14 (12.5%) 1 (0.9%) |
||
Vision | Excellent/Good Fair/Poor/Blind Unavailable |
99 (88.4%) 12 (10.7%) 1 (0.9%) |
||
MHIc | Depression and Anxiety | 78.3 ± 33.0 | 81 (21–100) | |
BOMCd Cognition Score |
<11 ≥11 Unavailable |
108 (96.4%) 1 (0.9%) 3 (2.7%) |
||
BMI (kg/m²)e | <22 ≥30 Unavailable |
17 (15.2%) 46 (41.1%) 49 (43.7%) |
||
Weight Loss | Greater than 5% in the last 6 months |
0 (0.0%) |