Drug intelligence / Profile preview

gemcitabine + FOLFIRINOX

Development stage
Unknown
Lead developer
University of Erlangen-Nürnberg Medical School
Modality
Small Molecules
Administration
Intravenous
01

Overview

This refers to a treatment strategy or combination of chemotherapy regimens evaluated in the CONKO-007 clinical trial for locally advanced, unresectable pancreatic cancer. The trial, sponsored by the University of Erlangen-Nürnberg Medical School, compares the efficacy of chemoradiotherapy (using gemcitabine) against chemotherapy alone (either gemcitabine or FOLFIRINOX) following an induction phase of chemotherapy. Gemcitabine is a nucleoside analog that inhibits DNA synthesis, while FOLFIRINOX is a multi-drug regimen consisting of oxaliplatin (DNA cross-linker), irinotecan (topoisomerase I inhibitor), leucovorin (folinic acid), and 5-fluorouracil (thymidylate synthase inhibitor). The study aims to determine if adding radiotherapy to these systemic treatments improves overall survival in patients with non-metastatic, non-resectable pancreatic ductal adenocarcinoma.

Other names
gemcitabine plus FOLFIRINOXCONKO-007 regimenCONKO007 regimenCONKO 007 regimen
02

Targets

TS (Thymidylate synthase)DNARNR (Ribonucleotide reductase)DNA polymerase familyTOP1 (DNA Topoisomerase I)

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