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gemcitabine + cisplatin + intensity-modulated radiation therapy (Sun Yat-sen University)

Development stage
Phase 3
Lead developer
Sun Yat-sen University
Modality
Small Molecules
Administration
Intravenous
01

Overview

This multimodal treatment regimen is designed for patients with locoregionally advanced nasopharyngeal carcinoma (NPC). It consists of an induction phase involving chemotherapy with **gemcitabine** and **cisplatin** (GP), followed by definitive **intensity-modulated radiation therapy** (IMRT), often with concurrent cisplatin. Developed and extensively studied by the Sun Yat-sen University Cancer Center, this protocol aims to reduce tumor burden and eliminate micrometastases before local radiation. Gemcitabine acts as a nucleoside analog that inhibits DNA synthesis by targeting ribonucleoside reductase and competing for DNA polymerase incorporation. Cisplatin is a platinum-based cytotoxic agent that induces DNA cross-linking, leading to apoptosis. IMRT provides highly precise radiation delivery, allowing for dose escalation to the tumor while minimizing toxicity to adjacent critical structures. Phase 3 clinical trials have demonstrated that this regimen significantly improves recurrence-free and overall survival compared to standard concurrent chemoradiotherapy alone in high-risk NPC patients.

Other names
GP induction chemotherapy followed by IMRTGemcitabine and Cisplatin induction chemotherapy plus IMRTSYSUCC NPC regimen
02

Targets

DNAENT1 (Solute carrier family 29 member 1)RNR (Ribonucleotide reductase)DNA polymerase family

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