OnCo

KEYNOTE-522 (pembrolizumab + chemotherapy, then adjuvant pembrolizumab)

Checked 2026-09-09

Stage II-III triple-negative breast cancer

One cycle

every 21 days × 4 · about 12 weeks in total
178141521Pembrolizumab: 200 mg, IntravenousPembrolizumabPaclitaxel: 80 mg/m², IntravenousPaclitaxelCarboplatin: AUC 5 day 1 (or AUC 1.5 weekly), IntravenousCarboplatinDoxorubicin: 60 mg/m² (or epirubicin 90 mg/m²), IntravenousDoxorubicinCyclophosphamide: 600 mg/m², IntravenousCyclophosphamide
21-day cycle × 4 paclitaxel-carboplatin then 4 AC/EC, surgery, then 9 adjuvant pembrolizumab (about 12 weeks)Intravenous

Components

DrugDoseRouteDays
Pembrolizumab
Monoclonal antibody (anti-PD-1)
200 mgIVD1
Paclitaxel
Cytotoxic chemotherapy (taxane)
80 mg/m²IVD1, 8, 15
Carboplatin
Cytotoxic chemotherapy (platinum)
AUC 5 day 1 (or AUC 1.5 weekly)IVD1
Doxorubicin
Cytotoxic chemotherapy (anthracycline)
60 mg/m² (or epirubicin 90 mg/m²)IVD1
Cyclophosphamide
Alkylating agent (oxazaphosphorine prodrug)
600 mg/m²IVD1
Cycles
4 paclitaxel-carboplatin then 4 AC/EC, surgery, then 9 adjuvant pembrolizumab
21-day cycle
Emetogenicity
High (>90%)
G-CSF
Consider (10-20% FN risk)

Notes

  • pCR 64.8% vs 51.2%; event-free survival and overall survival benefit confirmed at later analyses.
  • Immune-related endocrinopathies (thyroid, adrenal, hypophysitis) can be permanent; check baseline TSH and cortisol.

Used in

Source

KEYNOTE-522, NEJM 2020 (Schmid)

Reference doses for a typical adult from the cited protocol or label. Doses are adjusted for renal and hepatic function, age, performance status and prior toxicity, and institutional protocols vary. Verify against the current label and your local protocol before treating. Not medical advice.

Other regimens for these cancers