Table 1.
Characteristic, N (%) unless stated | Total N = 47 |
---|---|
Sex | |
Male | 0 |
Female | 47 (100) |
Ethnicity | |
Caucasian/White | 41 (87.2) |
Non-Caucasian/non-White | 3 (6.4) |
Age, years; median (range) | 48.0 (35–73) |
Baseline ECOG PS | |
0 | 25 (53.2) |
1 | 22 (46.8) |
Prior anticancer therapy | |
Chemotherapy | 45 (95.7) |
Immunotherapy | 1 (2.1) |
Other | 11 (23.4) |
Missing | 2 (4.3) |
Number of previous anticancer therapy regimens | |
Neoadjuvant | 16 (34.0) |
Adjuvant | 27 (57.4) |
1st line, metastatic disease | 24 (51.1) |
2nd line, metastatic disease | 10 (21.3) |
>2nd line, metastatic disease | 5 (10.6) |
Missing | 2 (4.3) |
TP53a | |
Wild type | 2 (4.3) |
Mutant | 34 (72.3) |
Missing | 11 (23.4) |
BRCA1/2b | |
Wild type | 31 (66) |
Mutant | 5 (10.6) |
Missing | 11 (23.4) |
Basal subtypec | |
Yes | 36 (76.6) |
No | 7 (14.9) |
Missing | 4 (8.5) |
ATM ataxia-telangiectasia mutated, BRCA1/2 breast cancer gene 1/2, ECOG PS Eastern Cooperative Oncology Group Performance Status, TP53 tumor protein 53.
aOnly patients with biomarker status determined by FoundationOne® CDx next generation sequencing were reported.
bPatients with unknown BRCA1/2 status were prospectively tested at screening by BRCAnalysis assay (Myriad Genetics); patients that were found to be BRCA1/2 germline mutant were still enrolled in the study.
cAssessment for basal subtype was performed retrospectively via PAM50 analysis (Prosigna).