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cyclophosphamide + doxorubicin + vincristine + prednisone + chidamide + tislelizumab

Development stage
Preclinical
Lead developer
Hengrui Pharmaceutical
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous, Oral
01

Overview

This is a multi-agent combination regimen consisting of six drugs: - Cyclophosphamide (an alkylating agent) - Doxorubicin (an anthracycline antibiotic) - Vincristine (a vinca alkaloid) - Prednisone (a synthetic glucocorticoid corticosteroid) - Chidamide (a histone deacetylase inhibitor, HDACi) - Tislelizumab (a monoclonal antibody targeting PD-1) The first four agents form the classic CHOP chemotherapy backbone, widely used for lymphomas. Cyclophosphamide crosslinks DNA to inhibit cell division; doxorubicin intercalates DNA and inhibits topoisomerase II; vincristine disrupts microtubule formation; prednisone induces apoptosis in certain cancer cells and modulates immune response[2][4][8]. Chidamide is an epigenetic modulator that inhibits histone deacetylases, leading to altered gene expression and apoptosis in malignant cells. Tislelizumab is an immune checkpoint inhibitor that blocks PD-1 on T-cells, enhancing anti-tumor immunity. This combination represents a novel approach integrating cytotoxic chemotherapy, epigenetic modulation, and immunotherapy. It may be under investigation for aggressive or refractory lymphomas or other hematologic malignancies where standard regimens are insufficient.

02

Targets

DNATOP2A (DNA topoisomerase II)HDAC1 (Histone Deacetylase 1)GR (Glucocorticoid receptor)TUBB (Tubulin (alpha and beta subunits))PDCD1 (Programmed cell death protein 1 receptor)

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