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. 2022 Jun 14;17(3):355–368. doi: 10.1007/s11523-022-00886-x

Table 1.

Clinicopathological characteristics and treatment outcomes

Clinicopathological characteristics No. of patients (%)
All patients; N = 52 Sunitinib; N = 34 Bevacizumab; N = 18
Median age 52; range 29–70 52; range 30–69 52; range 29–70
Post-menopausal 30 (58%) 20 (59%) 10 (55%)
Pre-menopausal 22 (42%) 14 (41%) 8 (45%)
Chinese 34 (65%) 23 (68%) 11 (61%)
Malay 10 (19%) 5 (15%) 5 (28%)
Indian 3 (6%) 3 (9%) 0 (0%)
Others 5 (10%) 3 (9%) 2 (11%)
TNBC 12 (23%) 8 (24%) 4 (22%)
Non TNBC (HER2−/HR+) 40 (77%) 26 (76%) 14 (78%)
Grade 1 2 (4%) 2 (6%) 0 (0%)
Grade 2 19 (36%) 9 (26%) 10 (55%)
Grade 3 31 (60%) 23 (68%) 8 (45%)
Clinical stage
Stage I 1 (2%) 0 (0%) 1 (6%)
Stage II 29 (55%) 19 (56%) 10 (55%)
Stage III 17 (33%) 10 (29%) 7 (39%)
Stage IV 5 (10%) 5 (15%) 0 (0%)
Non metastatic 47 (90%) 29 (85%) 18 (100%)
Metastatic 5 (10%) 5 (15%) 0 (0%)
Pathological response
Pathological complete response 2 (4%) 1 (3%) 1 (6%)
Residual tumor present 50 (96%) 33 (97%) 17 (94%)
Miller Payne histological response
Good 29 (56%) 18 (53%) 11 (61%)
Poor 15 (29%) 11 (32%) 4 (22%)
Unable to assessa 8 (15%) 5 (15%) 3 (17%)
Clinical objective response on CT imaging by RECIST
Clinical CR/PR 38 (73%) 23 (67%) 15 (83%)
Clinical stable disease 12 (23%) 9 (27%) 3 (17%)
Primary progression of disease 0 (0%) 0 (0%) 0 (0%)
No imaging for RECIST assessment done after treatment 2 (4%) 2 (6%) 0 (0%)
Dead 2 (4%) 1 (3%) 1 (6%)
Alive 50 (96%) 33 (97%) 17 (94%)
Stage I–III patients who developed relapse 4 (9%) 3 (10%) 1 (6%)
Stage I–III patients who remained disease free 43 (91%) 26 (90%) 17 (94%)
Stage IV patients who developed progression of disease 3 (60%) 3 (60%) 0
Stage IV patients who remained progression free after mastectomy and radiotherapy 2 (40%) 2 (40%) 0

CR/PR complete response/partial response; CT computed tomography; HER2− human epidermal growth factor receptor 2 negative; HR+ hormone receptor positive; IHC immunohistochemistry; RECIST response evaluation criteria in solid tumors

aMiller Payne score could not be assessed in patients if there was insufficient tissue after prior sectioning for IHC analysis or if the baseline tumor content was <5% in the baseline samples