Drug intelligence / Profile preview

capecitabine + oxaliplatin + toripalimab + surufatinib

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

Overview

This experimental combination regimen is being evaluated as a neoadjuvant therapy for patients with high-risk, mid-to-low localized rectal cancer. The regimen consists of short-course radiotherapy (SCRT) followed by CapeOX chemotherapy (a combination of capecitabine and oxaliplatin) integrated with toripalimab, a PD-1 inhibitor, and surufatinib, a small molecule tyrosine kinase inhibitor targeting VEGFR and FGFR. This multi-modal approach aims to improve pathological complete response (pCR) rates by combining cytotoxic chemotherapy, radiation, immune checkpoint blockade, and anti-angiogenic therapy. The study is sponsored by The First Hospital of Jilin University and explores whether the addition of surufatinib to the chemo-immunotherapy backbone enhances efficacy in high-risk locally advanced rectal cancer (LARC).

Other names
experimental group-The First Hospital of Jilin University-rectal cancerCapeOX + toripalimab + surufatinibSCRT followed by CapeOX + toripalimab + surufatinib
02

Targets

VEGFR4 (Vascular endothelial growth factor Receptor-3)TS (Thymidylate synthase)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)DNAFGFR1 (Fibroblast growth factor receptor 1)CSF1R (Macrophage colony-stimulating factor receptor)PDCD1 (Programmed cell death protein 1 receptor)

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