Drug intelligence / Profile preview

sunitinib + gemcitabine + paclitaxel + pembrolizumab

Development stage
Unknown
Lead developer
Hoosier Cancer Research Network
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Oral, Intravenous
01

Overview

SGP+P is a combination chemo-immunotherapy regimen consisting of sunitinib, gemcitabine, paclitaxel, and pembrolizumab. It has been primarily investigated for the treatment of advanced or metastatic urothelial carcinoma (bladder cancer). The regimen integrates the multi-targeted tyrosine kinase inhibitor sunitinib, which inhibits vascular endothelial growth factor receptors (VEGFR) and platelet-derived growth factor receptors (PDGFR) to disrupt tumor angiogenesis, with the cytotoxic chemotherapy agents gemcitabine and paclitaxel. Gemcitabine acts as a nucleoside analog that inhibits DNA synthesis, while paclitaxel stabilizes microtubules to prevent cell division. The addition of pembrolizumab, a monoclonal antibody targeting the programmed death receptor-1 (PD-1), serves to block the interaction between PD-1 and its ligands (PD-L1 and PD-L2), thereby reactivating the patient's immune system to recognize and attack malignant cells. This multi-pronged approach aims to overcome resistance and improve outcomes in patients with aggressive urothelial malignancies.

Other names
SGP plus pembrolizumabSGP-pembrolizumab
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)PDGFRB (Platelet-derived growth factor receptor beta)DNA polymerase familyRRM1TUBB (Tubulin (alpha and beta subunits))FLT3 (Fms related receptor tyrosine kinase 3)

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