Drug intelligence / Profile preview

pembrolizumab + paclitaxel + carboplatin + epirubicin + cyclophosphamide

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

Overview

This regimen represents the standard of care (SOC) neoadjuvant systemic therapy used in the LESLIE trial (NCT05840003) for patients with early-stage triple-negative breast cancer (TNBC). Developed and evaluated by Universitaire Ziekenhuizen KU Leuven, the regimen consists of a sequential treatment plan: four cycles of pembrolizumab (a PD-1 inhibitor) combined with paclitaxel (a microtubule stabilizer) and carboplatin (a DNA alkylating agent), followed by four cycles of epirubicin (an anthracycline) and cyclophosphamide (an alkylating agent) with continued pembrolizumab. The regimen aims to achieve a pathological complete response (pCR) by combining immunotherapy with cytotoxic chemotherapy, serving as the baseline against which lifestyle interventions like fasting-mimicking diets and exercise are tested.

Brand names
KeytrudaTaxolParaplatinEllenceCytoxan
Other names
SOCLESLIE trial SOC
02

Targets

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

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