Drug intelligence / Profile preview

pembrolizumab + nab-paclitaxel + doxorubicin + cyclophosphamide

Development stage
Unknown
Lead developer
Merck
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous
01

Overview

This is a **combination regimen** including four anticancer agents: pembrolizumab, nab-paclitaxel, doxorubicin, and cyclophosphamide, used primarily in the treatment of high-risk, early-stage or locally advanced triple-negative breast cancer (TNBC) and in investigational settings for other HER2-negative breast cancers. **Pembrolizumab** is a monoclonal antibody targeting PD-1, enabling T-cell mediated anti-tumor immunity (an immune checkpoint inhibitor). **Nab-paclitaxel** is an albumin-bound formulation of paclitaxel, a mitotic inhibitor targeting tubulin. **Doxorubicin** is an anthracycline antineoplastic agent acting primarily via DNA intercalation and topoisomerase II inhibition. **Cyclophosphamide** is an an alkylating agent that promotes cell death via DNA crosslinking. The combination leverages the immune-stimulating properties of pembrolizumab with the cytotoxic effects of chemotherapy to increase pathological complete response rates in the neoadjuvant or metastatic setting[1][5]. Clinical trials use this regimen or close variants to maximize responses in TNBC (notably NCT03289819[1]), although some studies substitute epirubicin for doxorubicin in the anthracycline component. The principal mechanism of benefit is synergistic immunotherapy and cytotoxic chemotherapy.

02

Targets

TOP2A (DNA topoisomerase II)TUBB (Tubulin (alpha and beta subunits))PDCD1 (Programmed cell death protein 1 receptor)DNA

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