Skip to main content
. 2018 May 29;119(1):4–11. doi: 10.1038/s41416-018-0126-6

Table 1.

Immune checkpoint inhibitors in metastatic breast cancer

Study Phase Checkpoint inhibitor Combination Population Number of patients PD-L1 selection ORR (RECIST 1.1)
KEYNOTE-01227 1b Pembrolizumab Nil

TNBC

; pre-treated

32 PD-L1 positive (expression in stroma or ≥1% tumour cells) 18.5%
KEYNOTE-08629, 30 2 Pembrolizumab Nil

TNBC

; Cohort A, pre-treated;

Cohort B, first line

Cohort A: 170

Cohort B: 52

Cohort A, unselected;

Cohort B, PD-L1 positive (combined positive score ≥1%)

Cohort A: 5%

Cohort B: 23%

Emens et al.31 1a Atezolizumab Nil

TNBC

; majority pre-treated

21 PD-L1 positive (≥5% of infiltrating immune cells) 24%
Schmid et al.25 1a Atezolizumab Nil

TNBC

; first line or pre-treated

115 Unselected 10%
Tolaney et al.32 1b/2 Pembrolizumab Eribulin

TNBC

; first line or pre-treated

39 Unselected 33.3%
Adams et al.34 1b Atezolizumab Nab-paclitaxel

TNBC

; first line or pre-treated

32 Unselected 42%
KEYNOTE-02836 1b Pembrolizumab Nil ER+/HER2-; pre-treated 25 PD-L1 positive (expression in stroma or ≥1% tumour cells) 12%
JAVELIN39 1b Avelumab Nil

Unselected

; pre-treated

168 Unselected 5.4%

Summary of recently presented studies of anti-PD1/PD-L1 therapy in metastatic breast cancer.

ORR objective response rate, TNBC triple-negative breast cancer