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

Table 2.

Immune checkpoint inhibitors in primary breast cancer

Study Phase Checkpoint inhibitor Chemotherapy Population No. of patients pCR (ypT0/is and ypN0)
I-SPY 243 2 Pembrolizumab Paclitaxel or paclitaxel/pembro followed by doxorubicin/cyclophosphamide

TNBC

; HR+/HER2-

; PD-L1 unselected

; tumour size > 2.5 cm; mammaprint high risk

(nodal involvement in 37.7% pembro, 43.9% control)

69 pembro, 180 control

TNBC: 60% pembro vs. 20% controla

HR+/HER2-: 34% pembro vs. 13% controla

KEYNOTE-17341 1b Pembrolizumab

A: pembro followed by pembro + nab-paclitaxel followed by pembro + doxorubicin/cyclophosphamide

. B: pembro followed by pembro + nab-paclitaxel + carboplatin followed by pembro + doxorubicin/cyclophosphamide

TNBC

; PD-L1 unselected

; locally advanced (primary tumour stage ≥T2 in 90%, nodal involvement in 75%)

20

Cohort A, 60%;

Cohort B, 90%

Pusztai et al.42 1 MEDI4736 MEDI4736 + nab-paclitaxel followed by dose dense doxorubicin/cyclophosphamide

TNBC

; PD-L1 unselected; stage I-III (primary tumour stage ≥T2 in 57%, nodal involvement in 57%)

7 71.4%

Recently presented studies of anti-PD1/PD-L1 agents in neoadjuvant breast cancer therapy.

pCR pathological complete response.

aEstimated pCR