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Gemcitabine + cisplatin + S-1

AstraZeneca · Phase 3 active Small molecule

This combination uses gemcitabine and cisplatin as DNA-damaging chemotherapy agents alongside S-1, an oral fluoropyrimidine, to inhibit cancer cell proliferation and survival through multiple pathways.

This combination uses gemcitabine and cisplatin as DNA-damaging chemotherapy agents alongside S-1, an oral fluoropyrimidine, to inhibit cancer cell proliferation and survival through multiple pathways. Used for Gastric cancer or gastroesophageal junction cancer (Phase 3 development).

At a glance

Generic nameGemcitabine + cisplatin + S-1
Also known asBackground Gemcitabine-based Chemotherapy Regimen., This regimen is not allowed for countries in the European Union.
SponsorAstraZeneca
Drug classChemotherapy combination (nucleoside analog + platinum agent + fluoropyrimidine)
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Gemcitabine is a nucleoside analog that inhibits ribonucleotide reductase and gets incorporated into DNA, causing chain termination. Cisplatin is a platinum-based alkylating agent that forms DNA cross-links, preventing replication. S-1 is a combination of tegafur (a prodrug of 5-fluorouracil), gimeracil (dihydropyrimidine dehydrogenase inhibitor), and oteracil (orotate phosphoribosyltransferase inhibitor) that enhances fluoropyrimidine activity by inhibiting its degradation and reducing gastrointestinal toxicity.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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