Drug intelligence / Profile preview

bendamustine + pomalidomide + sintilimab

Development stage
Unknown
Lead developer
The First Affiliated Hospital of Guangxi Medical University
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Oral, Intravenous
01

Overview

This combination therapy consists of the alkylating agent bendamustine, the immunomodulatory drug pomalidomide, and the PD-1 checkpoint inhibitor sintilimab. It is primarily investigated for the treatment of relapsed or refractory diffuse large B-cell lymphoma (R/R DLBCL). Bendamustine acts as a cytotoxic agent by inducing DNA cross-linking and subsequent apoptosis. Pomalidomide, a thalidomide analogue, binds to the cereblon E3 ubiquitin ligase complex, leading to the degradation of transcription factors Ikaros and Aiolos, which enhances T-cell and NK-cell mediated immunity while directly inhibiting tumor cell growth. Sintilimab is a monoclonal antibody that blocks the interaction between the PD-1 receptor on T-cells and its ligands, thereby restoring the anti-tumor immune response. The triplet regimen aims to leverage the synergistic effects of direct cytotoxicity, immunomodulation, and checkpoint blockade to overcome resistance in aggressive lymphomas.

Other names
bendamustinepomalidomidesintilimab
02

Targets

CRBN (Cereblon)DNAPDCD1 (Programmed cell death protein 1 receptor)

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